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Melvin Berger - Academia.edu
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class="u-taCenter"></div><div class="profile--tab_content_container js-tab-pane tab-pane active" id="all"><div class="profile--tab_heading_container js-section-heading" data-section="Papers" id="Papers"><h3 class="profile--tab_heading_container">Papers by Melvin Berger</h3></div><div class="js-work-strip profile--work_container" data-work-id="48834432"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/48834432/Isolation_and_Characterization_of_Complement_Receptor_Type_1_CR1_Storage_Vesicles_From_Human_Neutrophils_Using_Antibodies_to_the_Cytoplasmic_Tail_of_CR1"><img alt="Research paper thumbnail of Isolation and Characterization of Complement Receptor Type 1 (CR1) Storage Vesicles From Human Neutrophils Using Antibodies to the Cytoplasmic Tail of CR1" class="work-thumbnail" src="https://attachments.academia-assets.com/67253852/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/48834432/Isolation_and_Characterization_of_Complement_Receptor_Type_1_CR1_Storage_Vesicles_From_Human_Neutrophils_Using_Antibodies_to_the_Cytoplasmic_Tail_of_CR1">Isolation and Characterization of Complement Receptor Type 1 (CR1) Storage Vesicles From Human Neutrophils Using Antibodies to the Cytoplasmic Tail of CR1</a></div><div class="wp-workCard_item"><span>Blood</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Neutrophil (PMN) activation is associated with increased surface expression of several membrane p...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Neutrophil (PMN) activation is associated with increased surface expression of several membrane proteins that are translocated from intracellular pools. Indirect evidence suggests that the intracellular storage pools of complement receptor type 1 (CR1) in resting PMN are distinct from traditional granules and may be the secretory vesicles in which albumin is also stored, but it is not known if this compartment is homogeneous or heterogeneous. To isolate and characterize the CR1-containing vesicles, we used antibodies against unique sequences in the cytoplasmic tail of CR1. Affinity-purified IgG was used to adsorb CR1 storage vesicles from the light membrane fraction (纬-band) of nitrogen cavitates of resting PMN. The immunoadsorbent could quantitatively remove the CR1-containing vesicles, whereas control adsorbents with nonimmune IgG showed no specific binding of CR1. Immunoblots of specifically isolated vesicles also showed enrichment of albumin, decay-accelerating factor, Fc纬RIII, ...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="f4618ea5165916ed4adac9f40e156c4d" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":67253852,"asset_id":48834432,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/67253852/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834432"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834432"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834432; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=48834431]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":48834431,"title":"Update on C1 Esterase Inhibitor (C1-INH) in Human Solid Organ Transplantation","internal_url":"https://www.academia.edu/48834431/Update_on_C1_Esterase_Inhibitor_C1_INH_in_Human_Solid_Organ_Transplantation","owner_id":38990937,"coauthors_can_edit":true,"owner":{"id":38990937,"first_name":"Melvin","middle_initials":null,"last_name":"Berger","page_name":"BergerMelvin","domain_name":"independent","created_at":"2015-11-23T12:17:10.855-08:00","display_name":"Melvin Berger","url":"https://independent.academia.edu/BergerMelvin"},"attachments":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="48834430"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/48834430/Alpha_1_antitrypsin_in_cell_and_organ_transplantation"><img alt="Research paper thumbnail of Alpha-1-antitrypsin in cell and organ transplantation" class="work-thumbnail" src="https://attachments.academia-assets.com/67253893/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/48834430/Alpha_1_antitrypsin_in_cell_and_organ_transplantation">Alpha-1-antitrypsin in cell and organ transplantation</a></div><div class="wp-workCard_item"><span>American Journal of Transplantation</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Despite significant advances in surgical technique and immunosuppression, challenges continue to ...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Despite significant advances in surgical technique and immunosuppression, challenges continue to restrict the number of transplants. Although the number of transplants performed each year in the United States is increasing, the number of people on waiting lists has nearly doubled in the past 15 years. 1 Improving the viability of donor organs by reducing the damage caused by ischemia-reperfusion injury (IRI) and activation of the innate immune system are thus key areas of ongoing research. Alpha-1-antitrypsin (AAT) is a serine protease inhibitor and acute phase reactant produced mainly by the liver that limits tissue damage caused by neutrophil elastase and other extracellular enzymes. 2-4 Consistent with this role, plasma concentrations of AAT can increase up to 4-fold in response to inflammatory stimuli. Mutations in AAT can cause emphysema due to deficiency in circulating AAT, and/or liver disease likely due to a "misfolded protein response." 2-4 AAT-deficient patients may also experience extrapulmonary pathologies, particularly panniculitis</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="aa7859e322f4593e08a5b5184be77ea9" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":67253893,"asset_id":48834430,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/67253893/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834430"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834430"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834430; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="48834429"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/48834429/Antibodies_to_vaccine_antigens_in_pooled_polyclonal_human_IgG_products"><img alt="Research paper thumbnail of Antibodies to vaccine antigens in pooled polyclonal human IgG products" class="work-thumbnail" src="https://attachments.academia-assets.com/67253897/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/48834429/Antibodies_to_vaccine_antigens_in_pooled_polyclonal_human_IgG_products">Antibodies to vaccine antigens in pooled polyclonal human IgG products</a></div><div class="wp-workCard_item"><span>Transfusion</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">* In this table, data from Wu et al. 42 is for products made from US plasma only.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="b2890bdaf32e2d0123899e6abc854b9a" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":67253897,"asset_id":48834429,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/67253897/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834429"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834429"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834429; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="48834428"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" rel="nofollow" href="https://www.academia.edu/48834428/_content_IgPro20_the_Polyneuropathy_and_Treatment_with_Hizentra_study_PATH_and_the_treatment_of_chronic_inflammatory_demyelinating_polyradiculoneuropathy_with_subcutaneous_IgG_sup_content_"><img alt="Research paper thumbnail of {"__content__"=>"IgPro20, the Polyneuropathy and Treatment with Hizentra study (PATH), and the treatment of chronic inflammatory demyelinating polyradiculoneuropathy with subcutaneous IgG.", "sup"=>{"__content__"=>"庐"}}" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/48834428/_content_IgPro20_the_Polyneuropathy_and_Treatment_with_Hizentra_study_PATH_and_the_treatment_of_chronic_inflammatory_demyelinating_polyradiculoneuropathy_with_subcutaneous_IgG_sup_content_">{"__content__"=>"IgPro20, the Polyneuropathy and Treatment with Hizentra study (PATH), and the treatment of chronic inflammatory demyelinating polyradiculoneuropathy with subcutaneous IgG.", "sup"=>{"__content__"=>"庐"}}</a></div><div class="wp-workCard_item"><span>Immunotherapy</span><span>, Jan 16, 2018</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Subcutaneous IgG (SCIG) administration may be preferred over the intravenous route (IVIG) in chro...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Subcutaneous IgG (SCIG) administration may be preferred over the intravenous route (IVIG) in chronic inflammatory demyelinating polyneuropathy (CIDP) because it minimizes &#39;end of cycle&#39; treatment-related fluctuations, reduces systemic adverse effects, improves convenience/quality of life and potentially lowers overall costs. Early reports of the use of highly concentrated SCIG preparations suggested they were effective and well-tolerated in chronic inflammatory demyelinating polyneuropathy. This was confirmed in the Polyneuropathy and Treatment with Hizentra study of 172 subjects randomized to receive maintenance therapy with placebo or one of two doses of IgPro20 (20% IgG stabilized with L-Proline) for 6聽months. Risk of relapse was reduced by SCIG in a dose-related manner as compared with placebo. A total of 88% of polyneuropathy and treatment with hizentra subjects felt the subcutaneous method was聽&#39;easy to learn&#39;. Local adverse events were mostly mild or moderate, ...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834428"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834428"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834428; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=48834428]").text(description); $(".js-view-count[data-work-id=48834428]").attr('title', description).tooltip(); 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="48834427"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/48834427/Individualized_immunoglobulin_therapy_in_chronic_immune_mediated_peripheral_neuropathies"><img alt="Research paper thumbnail of Individualized immunoglobulin therapy in chronic immune-mediated peripheral neuropathies" class="work-thumbnail" src="https://attachments.academia-assets.com/67253895/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/48834427/Individualized_immunoglobulin_therapy_in_chronic_immune_mediated_peripheral_neuropathies">Individualized immunoglobulin therapy in chronic immune-mediated peripheral neuropathies</a></div><div class="wp-workCard_item"><span>Journal of the peripheral nervous system : JPNS</span><span>, Jan 23, 2018</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Despite the well-recognized importance of immunoglobulin therapy individualization during the tre...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Despite the well-recognized importance of immunoglobulin therapy individualization during the treatment of chronic inflammatory demyelinating polyneuropathy (CIDP), the pathway to best achieve optimization is unknown. There are many pharmacokinetic and immunobiologic variables that can potentially influence the appropriateness of any individual therapy. Although identification of specific autoantibodies and their targets has only been accomplished in a minority of patients with CIDP, already the diagnostic and treatment implications of specific autoantibody detection are being realized. Individual variability in IgG pharmacokinetic properties including IgG catabolic rates and distribution, as well as the IgG level necessary for disease control also require consideration during the optimization process. For optimization to be successful there must be a measure of treatment response that has a clinically meaningful interpretation. There are currently available well-defined and validat...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="f58237164d2d9db3dd4b22df54cf9bfc" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":67253895,"asset_id":48834427,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/67253895/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834427"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834427"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834427; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="48834426"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/48834426/Primary_immune_deficiency_diseases_as_unrecognized_causes_of_chronic_respiratory_disease"><img alt="Research paper thumbnail of Primary immune deficiency diseases as unrecognized causes of chronic respiratory disease" class="work-thumbnail" src="https://attachments.academia-assets.com/67253894/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/48834426/Primary_immune_deficiency_diseases_as_unrecognized_causes_of_chronic_respiratory_disease">Primary immune deficiency diseases as unrecognized causes of chronic respiratory disease</a></div><div class="wp-workCard_item"><span>Respiratory medicine</span><span>, 2017</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">More than half of all primary immune deficiency diseases (PIDD) affect antibody production and ar...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">More than half of all primary immune deficiency diseases (PIDD) affect antibody production and are well known as causes of recurrent sinusitis and lung infections. Chronic and recurrent infections of the upper and/or lower airways can contribute to inflammatory and obstructive processes in the lower airways which are initially reversible and considered &quot;asthma&quot;, but can eventually cause irreversible remodeling and chronic obstructive pulmonary disease (COPD). Conversely, several lines of evidence suggest that many patients who present with a diagnosis of asthma have an increased incidence of infection, suggesting underlying host-defense defects. Asthma and respiratory infections in the first decades of life are recognized as risk factors for development of COPD, but when patients present with COPD as adults, underlying primary immune deficiency disease may be unrecognized. Detection of PIDD as a potentially treatable underlying contributor to recurrent/acute exacerbations ...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="b6241641781cd44bc5510045e4143f98" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":67253894,"asset_id":48834426,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/67253894/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834426"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834426"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834426; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "b6241641781cd44bc5510045e4143f98" } } $('.js-work-strip[data-work-id=48834426]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":48834426,"title":"Primary immune deficiency diseases as unrecognized causes of chronic respiratory disease","internal_url":"https://www.academia.edu/48834426/Primary_immune_deficiency_diseases_as_unrecognized_causes_of_chronic_respiratory_disease","owner_id":38990937,"coauthors_can_edit":true,"owner":{"id":38990937,"first_name":"Melvin","middle_initials":null,"last_name":"Berger","page_name":"BergerMelvin","domain_name":"independent","created_at":"2015-11-23T12:17:10.855-08:00","display_name":"Melvin Berger","url":"https://independent.academia.edu/BergerMelvin"},"attachments":[{"id":67253894,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/67253894/thumbnails/1.jpg","file_name":"pdf.pdf","download_url":"https://www.academia.edu/attachments/67253894/download_file","bulk_download_file_name":"Primary_immune_deficiency_diseases_as_un.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/67253894/pdf-libre.pdf?1620414305=\u0026response-content-disposition=attachment%3B+filename%3DPrimary_immune_deficiency_diseases_as_un.pdf\u0026Expires=1739840592\u0026Signature=drRe-AHLUoDFzbTFB5MTUX3CKa2Orc9cz0UeGywYNLIVmF6~owDSw3Le8sF3LNt3ub6l2lGJcWBxT7z4OhRrMstKQ0tLoXhNx5qKNHEaTLesnotDjH6j0Lcn3Pt4paNGH8RgaxzIrit4avnxCPn0xSbJpwxoGiHgLKJZhLJPIJAxneRfwZSI1MXOUmwDOywA8c1Dy~5cwVpO1ogUwbgSGK9J-AAIa2YhQ6awhlgV6fS2cqecj0B4eF9heCRS7OfMDCcMOPwuFNIoLgfSvOoPEn6-xkCH5Fd1smjjDSrmXCCVzP9qstx37MnEqRbD6SkJeYLuCHcXhKr2K6S3QCcKCA__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="48834425"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" rel="nofollow" href="https://www.academia.edu/48834425/Immunoglobulin_therapy_in_hematologic_neoplasms_and_after_hematopoietic_cell_transplantation"><img alt="Research paper thumbnail of Immunoglobulin therapy in hematologic neoplasms and after hematopoietic cell transplantation" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/48834425/Immunoglobulin_therapy_in_hematologic_neoplasms_and_after_hematopoietic_cell_transplantation">Immunoglobulin therapy in hematologic neoplasms and after hematopoietic cell transplantation</a></div><div class="wp-workCard_item"><span>Blood Reviews</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Immunoglobulins are used to prevent or reduce infection risk in primary immune deficiencies and i...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Immunoglobulins are used to prevent or reduce infection risk in primary immune deficiencies and in settings which exploit its anti-inflammatory and immune-modulatory effects. Rigorous proof of immunoglobulin efficacy in persons with lympho-proliferative neoplasms, plasma cell myeloma, and persons receiving hematopoietic cell transplants is lacking despite many clinical trials. Further, there are few consensus guidelines or algorithms for use in these conditions. Rapid development of new therapies targeting B-cell signaling and survival pathways and increased use of chimeric antigen receptor T-cell (CAR-T) therapy will likely result in more acquired deficiencies of humoral immunity and infections in persons with cancer. We review immunoglobulin formulations and discuss efficacy and potential adverse effects in the context of preventing infections and in graft-versus-host disease. We suggest an algorithm for evaluating acquired deficiencies of humoral immunity in persons with hematologic neoplasms and recommend appropriate use of immunoglobulin therapy.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834425"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834425"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834425; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); 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</script> <div class="js-work-strip profile--work_container" data-work-id="48834422"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" rel="nofollow" href="https://www.academia.edu/48834422/Assessment_of_protein_antibody_response_in_patients_with_suspected_immune_deficiency"><img alt="Research paper thumbnail of Assessment of protein antibody response in patients with suspected immune deficiency" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/48834422/Assessment_of_protein_antibody_response_in_patients_with_suspected_immune_deficiency">Assessment of protein antibody response in patients with suspected immune deficiency</a></div><div class="wp-workCard_item"><span>Annals of Allergy Asthma Immunology Official Publication of the American College of Allergy Asthma Immunology</span><span>, Mar 1, 2008</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834422"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834422"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834422; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="48834420"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" rel="nofollow" href="https://www.academia.edu/48834420/Intravenous_%CE%B3_globulin_therapy_in_bronchial_asthma"><img alt="Research paper thumbnail of Intravenous 纬-globulin therapy in bronchial asthma" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/48834420/Intravenous_%CE%B3_globulin_therapy_in_bronchial_asthma">Intravenous 纬-globulin therapy in bronchial asthma</a></div><div class="wp-workCard_item"><span>Allergy and Asthma Proceedings</span><span>, 2002</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834420"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834420"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834420; 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</script> <div class="js-work-strip profile--work_container" data-work-id="48834418"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" rel="nofollow" href="https://www.academia.edu/48834418/Subcutaneous_Immunoglobulin_Replacement_Therapy_in_Infants_and_Children_with_Primary_Immunodeficiencies"><img alt="Research paper thumbnail of Subcutaneous Immunoglobulin Replacement Therapy in Infants and Children with Primary Immunodeficiencies" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/48834418/Subcutaneous_Immunoglobulin_Replacement_Therapy_in_Infants_and_Children_with_Primary_Immunodeficiencies">Subcutaneous Immunoglobulin Replacement Therapy in Infants and Children with Primary Immunodeficiencies</a></div><div class="wp-workCard_item"><span>Journal of Allergy and Clinical Immunology</span><span>, Feb 1, 2011</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834418"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834418"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834418; 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</script> <div class="js-work-strip profile--work_container" data-work-id="48834417"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" rel="nofollow" href="https://www.academia.edu/48834417/Immunoglobulins_in_the_newborn"><img alt="Research paper thumbnail of Immunoglobulins in the newborn" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/48834417/Immunoglobulins_in_the_newborn">Immunoglobulins in the newborn</a></div><div class="wp-workCard_item"><span>Curr Opin Infect Dis</span><span>, 1991</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834417"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834417"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834417; 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ABSENCE OF THE THIRD COMPONENT OF COMPLEMENT Melvin Berger, MD, Ph.D., James E. Balow, MD, Cu...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">... ABSENCE OF THE THIRD COMPONENT OF COMPLEMENT Melvin Berger, MD, Ph.D., James E. Balow, MD, Curtis B. Wilson, MD, and Michael M. Frank, MD THE third component of complement (C3) is criti-cally involved in host defense and the mainte-nance of normal ...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834415"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834415"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834415; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=48834415]").text(description); 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</script> <div class="js-work-strip profile--work_container" data-work-id="48834414"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" rel="nofollow" href="https://www.academia.edu/48834414/_74_Third_component_of_human_complement_C3"><img alt="Research paper thumbnail of [74] Third component of human complement: C3" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/48834414/_74_Third_component_of_human_complement_C3">[74] Third component of human complement: C3</a></div><div class="wp-workCard_item"><span>Methods in Enzymology</span><span>, 1990</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834414"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834414"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834414; 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</script> </div><div class="profile--tab_content_container js-tab-pane tab-pane" data-section-id="4121119" id="papers"><div class="js-work-strip profile--work_container" data-work-id="48834432"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/48834432/Isolation_and_Characterization_of_Complement_Receptor_Type_1_CR1_Storage_Vesicles_From_Human_Neutrophils_Using_Antibodies_to_the_Cytoplasmic_Tail_of_CR1"><img alt="Research paper thumbnail of Isolation and Characterization of Complement Receptor Type 1 (CR1) Storage Vesicles From Human Neutrophils Using Antibodies to the Cytoplasmic Tail of CR1" class="work-thumbnail" src="https://attachments.academia-assets.com/67253852/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/48834432/Isolation_and_Characterization_of_Complement_Receptor_Type_1_CR1_Storage_Vesicles_From_Human_Neutrophils_Using_Antibodies_to_the_Cytoplasmic_Tail_of_CR1">Isolation and Characterization of Complement Receptor Type 1 (CR1) Storage Vesicles From Human Neutrophils Using Antibodies to the Cytoplasmic Tail of CR1</a></div><div class="wp-workCard_item"><span>Blood</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Neutrophil (PMN) activation is associated with increased surface expression of several membrane p...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Neutrophil (PMN) activation is associated with increased surface expression of several membrane proteins that are translocated from intracellular pools. Indirect evidence suggests that the intracellular storage pools of complement receptor type 1 (CR1) in resting PMN are distinct from traditional granules and may be the secretory vesicles in which albumin is also stored, but it is not known if this compartment is homogeneous or heterogeneous. To isolate and characterize the CR1-containing vesicles, we used antibodies against unique sequences in the cytoplasmic tail of CR1. Affinity-purified IgG was used to adsorb CR1 storage vesicles from the light membrane fraction (纬-band) of nitrogen cavitates of resting PMN. The immunoadsorbent could quantitatively remove the CR1-containing vesicles, whereas control adsorbents with nonimmune IgG showed no specific binding of CR1. Immunoblots of specifically isolated vesicles also showed enrichment of albumin, decay-accelerating factor, Fc纬RIII, ...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="f4618ea5165916ed4adac9f40e156c4d" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":67253852,"asset_id":48834432,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/67253852/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834432"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834432"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834432; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "-1" } } $('.js-work-strip[data-work-id=48834431]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":48834431,"title":"Update on C1 Esterase Inhibitor (C1-INH) in Human Solid Organ Transplantation","internal_url":"https://www.academia.edu/48834431/Update_on_C1_Esterase_Inhibitor_C1_INH_in_Human_Solid_Organ_Transplantation","owner_id":38990937,"coauthors_can_edit":true,"owner":{"id":38990937,"first_name":"Melvin","middle_initials":null,"last_name":"Berger","page_name":"BergerMelvin","domain_name":"independent","created_at":"2015-11-23T12:17:10.855-08:00","display_name":"Melvin Berger","url":"https://independent.academia.edu/BergerMelvin"},"attachments":[]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="48834430"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/48834430/Alpha_1_antitrypsin_in_cell_and_organ_transplantation"><img alt="Research paper thumbnail of Alpha-1-antitrypsin in cell and organ transplantation" class="work-thumbnail" src="https://attachments.academia-assets.com/67253893/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/48834430/Alpha_1_antitrypsin_in_cell_and_organ_transplantation">Alpha-1-antitrypsin in cell and organ transplantation</a></div><div class="wp-workCard_item"><span>American Journal of Transplantation</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Despite significant advances in surgical technique and immunosuppression, challenges continue to ...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Despite significant advances in surgical technique and immunosuppression, challenges continue to restrict the number of transplants. Although the number of transplants performed each year in the United States is increasing, the number of people on waiting lists has nearly doubled in the past 15 years. 1 Improving the viability of donor organs by reducing the damage caused by ischemia-reperfusion injury (IRI) and activation of the innate immune system are thus key areas of ongoing research. Alpha-1-antitrypsin (AAT) is a serine protease inhibitor and acute phase reactant produced mainly by the liver that limits tissue damage caused by neutrophil elastase and other extracellular enzymes. 2-4 Consistent with this role, plasma concentrations of AAT can increase up to 4-fold in response to inflammatory stimuli. Mutations in AAT can cause emphysema due to deficiency in circulating AAT, and/or liver disease likely due to a "misfolded protein response." 2-4 AAT-deficient patients may also experience extrapulmonary pathologies, particularly panniculitis</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="aa7859e322f4593e08a5b5184be77ea9" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":67253893,"asset_id":48834430,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/67253893/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834430"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834430"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834430; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="48834429"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/48834429/Antibodies_to_vaccine_antigens_in_pooled_polyclonal_human_IgG_products"><img alt="Research paper thumbnail of Antibodies to vaccine antigens in pooled polyclonal human IgG products" class="work-thumbnail" src="https://attachments.academia-assets.com/67253897/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/48834429/Antibodies_to_vaccine_antigens_in_pooled_polyclonal_human_IgG_products">Antibodies to vaccine antigens in pooled polyclonal human IgG products</a></div><div class="wp-workCard_item"><span>Transfusion</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">* In this table, data from Wu et al. 42 is for products made from US plasma only.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="b2890bdaf32e2d0123899e6abc854b9a" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":67253897,"asset_id":48834429,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/67253897/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834429"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834429"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834429; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="48834428"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" rel="nofollow" href="https://www.academia.edu/48834428/_content_IgPro20_the_Polyneuropathy_and_Treatment_with_Hizentra_study_PATH_and_the_treatment_of_chronic_inflammatory_demyelinating_polyradiculoneuropathy_with_subcutaneous_IgG_sup_content_"><img alt="Research paper thumbnail of {"__content__"=>"IgPro20, the Polyneuropathy and Treatment with Hizentra study (PATH), and the treatment of chronic inflammatory demyelinating polyradiculoneuropathy with subcutaneous IgG.", "sup"=>{"__content__"=>"庐"}}" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/48834428/_content_IgPro20_the_Polyneuropathy_and_Treatment_with_Hizentra_study_PATH_and_the_treatment_of_chronic_inflammatory_demyelinating_polyradiculoneuropathy_with_subcutaneous_IgG_sup_content_">{"__content__"=>"IgPro20, the Polyneuropathy and Treatment with Hizentra study (PATH), and the treatment of chronic inflammatory demyelinating polyradiculoneuropathy with subcutaneous IgG.", "sup"=>{"__content__"=>"庐"}}</a></div><div class="wp-workCard_item"><span>Immunotherapy</span><span>, Jan 16, 2018</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Subcutaneous IgG (SCIG) administration may be preferred over the intravenous route (IVIG) in chro...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Subcutaneous IgG (SCIG) administration may be preferred over the intravenous route (IVIG) in chronic inflammatory demyelinating polyneuropathy (CIDP) because it minimizes &#39;end of cycle&#39; treatment-related fluctuations, reduces systemic adverse effects, improves convenience/quality of life and potentially lowers overall costs. Early reports of the use of highly concentrated SCIG preparations suggested they were effective and well-tolerated in chronic inflammatory demyelinating polyneuropathy. This was confirmed in the Polyneuropathy and Treatment with Hizentra study of 172 subjects randomized to receive maintenance therapy with placebo or one of two doses of IgPro20 (20% IgG stabilized with L-Proline) for 6聽months. Risk of relapse was reduced by SCIG in a dose-related manner as compared with placebo. A total of 88% of polyneuropathy and treatment with hizentra subjects felt the subcutaneous method was聽&#39;easy to learn&#39;. Local adverse events were mostly mild or moderate, ...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834428"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834428"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834428; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=48834428]").text(description); $(".js-view-count[data-work-id=48834428]").attr('title', description).tooltip(); 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="48834427"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/48834427/Individualized_immunoglobulin_therapy_in_chronic_immune_mediated_peripheral_neuropathies"><img alt="Research paper thumbnail of Individualized immunoglobulin therapy in chronic immune-mediated peripheral neuropathies" class="work-thumbnail" src="https://attachments.academia-assets.com/67253895/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/48834427/Individualized_immunoglobulin_therapy_in_chronic_immune_mediated_peripheral_neuropathies">Individualized immunoglobulin therapy in chronic immune-mediated peripheral neuropathies</a></div><div class="wp-workCard_item"><span>Journal of the peripheral nervous system : JPNS</span><span>, Jan 23, 2018</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Despite the well-recognized importance of immunoglobulin therapy individualization during the tre...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Despite the well-recognized importance of immunoglobulin therapy individualization during the treatment of chronic inflammatory demyelinating polyneuropathy (CIDP), the pathway to best achieve optimization is unknown. There are many pharmacokinetic and immunobiologic variables that can potentially influence the appropriateness of any individual therapy. Although identification of specific autoantibodies and their targets has only been accomplished in a minority of patients with CIDP, already the diagnostic and treatment implications of specific autoantibody detection are being realized. Individual variability in IgG pharmacokinetic properties including IgG catabolic rates and distribution, as well as the IgG level necessary for disease control also require consideration during the optimization process. For optimization to be successful there must be a measure of treatment response that has a clinically meaningful interpretation. There are currently available well-defined and validat...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="f58237164d2d9db3dd4b22df54cf9bfc" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":67253895,"asset_id":48834427,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/67253895/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834427"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834427"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834427; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="48834426"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" href="https://www.academia.edu/48834426/Primary_immune_deficiency_diseases_as_unrecognized_causes_of_chronic_respiratory_disease"><img alt="Research paper thumbnail of Primary immune deficiency diseases as unrecognized causes of chronic respiratory disease" class="work-thumbnail" src="https://attachments.academia-assets.com/67253894/thumbnails/1.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" href="https://www.academia.edu/48834426/Primary_immune_deficiency_diseases_as_unrecognized_causes_of_chronic_respiratory_disease">Primary immune deficiency diseases as unrecognized causes of chronic respiratory disease</a></div><div class="wp-workCard_item"><span>Respiratory medicine</span><span>, 2017</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">More than half of all primary immune deficiency diseases (PIDD) affect antibody production and ar...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">More than half of all primary immune deficiency diseases (PIDD) affect antibody production and are well known as causes of recurrent sinusitis and lung infections. Chronic and recurrent infections of the upper and/or lower airways can contribute to inflammatory and obstructive processes in the lower airways which are initially reversible and considered &quot;asthma&quot;, but can eventually cause irreversible remodeling and chronic obstructive pulmonary disease (COPD). Conversely, several lines of evidence suggest that many patients who present with a diagnosis of asthma have an increased incidence of infection, suggesting underlying host-defense defects. Asthma and respiratory infections in the first decades of life are recognized as risk factors for development of COPD, but when patients present with COPD as adults, underlying primary immune deficiency disease may be unrecognized. Detection of PIDD as a potentially treatable underlying contributor to recurrent/acute exacerbations ...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><a id="b6241641781cd44bc5510045e4143f98" class="wp-workCard--action" rel="nofollow" data-click-track="profile-work-strip-download" data-download="{"attachment_id":67253894,"asset_id":48834426,"asset_type":"Work","button_location":"profile"}" href="https://www.academia.edu/attachments/67253894/download_file?s=profile"><span><i class="fa fa-arrow-down"></i></span><span>Download</span></a><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834426"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834426"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834426; 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dispatcherData = { dispatcher: window.WowProfile.dispatcher, downloadLinkId: "b6241641781cd44bc5510045e4143f98" } } $('.js-work-strip[data-work-id=48834426]').each(function() { if (!$(this).data('initialized')) { new WowProfile.WorkStripView({ el: this, workJSON: {"id":48834426,"title":"Primary immune deficiency diseases as unrecognized causes of chronic respiratory disease","internal_url":"https://www.academia.edu/48834426/Primary_immune_deficiency_diseases_as_unrecognized_causes_of_chronic_respiratory_disease","owner_id":38990937,"coauthors_can_edit":true,"owner":{"id":38990937,"first_name":"Melvin","middle_initials":null,"last_name":"Berger","page_name":"BergerMelvin","domain_name":"independent","created_at":"2015-11-23T12:17:10.855-08:00","display_name":"Melvin Berger","url":"https://independent.academia.edu/BergerMelvin"},"attachments":[{"id":67253894,"title":"","file_type":"pdf","scribd_thumbnail_url":"https://attachments.academia-assets.com/67253894/thumbnails/1.jpg","file_name":"pdf.pdf","download_url":"https://www.academia.edu/attachments/67253894/download_file","bulk_download_file_name":"Primary_immune_deficiency_diseases_as_un.pdf","bulk_download_url":"https://d1wqtxts1xzle7.cloudfront.net/67253894/pdf-libre.pdf?1620414305=\u0026response-content-disposition=attachment%3B+filename%3DPrimary_immune_deficiency_diseases_as_un.pdf\u0026Expires=1739840592\u0026Signature=drRe-AHLUoDFzbTFB5MTUX3CKa2Orc9cz0UeGywYNLIVmF6~owDSw3Le8sF3LNt3ub6l2lGJcWBxT7z4OhRrMstKQ0tLoXhNx5qKNHEaTLesnotDjH6j0Lcn3Pt4paNGH8RgaxzIrit4avnxCPn0xSbJpwxoGiHgLKJZhLJPIJAxneRfwZSI1MXOUmwDOywA8c1Dy~5cwVpO1ogUwbgSGK9J-AAIa2YhQ6awhlgV6fS2cqecj0B4eF9heCRS7OfMDCcMOPwuFNIoLgfSvOoPEn6-xkCH5Fd1smjjDSrmXCCVzP9qstx37MnEqRbD6SkJeYLuCHcXhKr2K6S3QCcKCA__\u0026Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA"}]}, dispatcherData: dispatcherData }); $(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="48834425"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" rel="nofollow" href="https://www.academia.edu/48834425/Immunoglobulin_therapy_in_hematologic_neoplasms_and_after_hematopoietic_cell_transplantation"><img alt="Research paper thumbnail of Immunoglobulin therapy in hematologic neoplasms and after hematopoietic cell transplantation" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/48834425/Immunoglobulin_therapy_in_hematologic_neoplasms_and_after_hematopoietic_cell_transplantation">Immunoglobulin therapy in hematologic neoplasms and after hematopoietic cell transplantation</a></div><div class="wp-workCard_item"><span>Blood Reviews</span></div><div class="wp-workCard_item"><span class="js-work-more-abstract-truncated">Immunoglobulins are used to prevent or reduce infection risk in primary immune deficiencies and i...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">Immunoglobulins are used to prevent or reduce infection risk in primary immune deficiencies and in settings which exploit its anti-inflammatory and immune-modulatory effects. Rigorous proof of immunoglobulin efficacy in persons with lympho-proliferative neoplasms, plasma cell myeloma, and persons receiving hematopoietic cell transplants is lacking despite many clinical trials. Further, there are few consensus guidelines or algorithms for use in these conditions. Rapid development of new therapies targeting B-cell signaling and survival pathways and increased use of chimeric antigen receptor T-cell (CAR-T) therapy will likely result in more acquired deficiencies of humoral immunity and infections in persons with cancer. We review immunoglobulin formulations and discuss efficacy and potential adverse effects in the context of preventing infections and in graft-versus-host disease. We suggest an algorithm for evaluating acquired deficiencies of humoral immunity in persons with hematologic neoplasms and recommend appropriate use of immunoglobulin therapy.</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834425"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834425"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834425; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); 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</script> <div class="js-work-strip profile--work_container" data-work-id="48834422"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" rel="nofollow" href="https://www.academia.edu/48834422/Assessment_of_protein_antibody_response_in_patients_with_suspected_immune_deficiency"><img alt="Research paper thumbnail of Assessment of protein antibody response in patients with suspected immune deficiency" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/48834422/Assessment_of_protein_antibody_response_in_patients_with_suspected_immune_deficiency">Assessment of protein antibody response in patients with suspected immune deficiency</a></div><div class="wp-workCard_item"><span>Annals of Allergy Asthma Immunology Official Publication of the American College of Allergy Asthma Immunology</span><span>, Mar 1, 2008</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834422"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834422"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834422; 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$(this).data('initialized', true); } }); $a.trackClickSource(".js-work-strip-work-link", "profile_work_strip") }); </script> <div class="js-work-strip profile--work_container" data-work-id="48834420"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" rel="nofollow" href="https://www.academia.edu/48834420/Intravenous_%CE%B3_globulin_therapy_in_bronchial_asthma"><img alt="Research paper thumbnail of Intravenous 纬-globulin therapy in bronchial asthma" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/48834420/Intravenous_%CE%B3_globulin_therapy_in_bronchial_asthma">Intravenous 纬-globulin therapy in bronchial asthma</a></div><div class="wp-workCard_item"><span>Allergy and Asthma Proceedings</span><span>, 2002</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834420"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834420"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834420; 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</script> <div class="js-work-strip profile--work_container" data-work-id="48834418"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" rel="nofollow" href="https://www.academia.edu/48834418/Subcutaneous_Immunoglobulin_Replacement_Therapy_in_Infants_and_Children_with_Primary_Immunodeficiencies"><img alt="Research paper thumbnail of Subcutaneous Immunoglobulin Replacement Therapy in Infants and Children with Primary Immunodeficiencies" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/48834418/Subcutaneous_Immunoglobulin_Replacement_Therapy_in_Infants_and_Children_with_Primary_Immunodeficiencies">Subcutaneous Immunoglobulin Replacement Therapy in Infants and Children with Primary Immunodeficiencies</a></div><div class="wp-workCard_item"><span>Journal of Allergy and Clinical Immunology</span><span>, Feb 1, 2011</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834418"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834418"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834418; 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</script> <div class="js-work-strip profile--work_container" data-work-id="48834417"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" rel="nofollow" href="https://www.academia.edu/48834417/Immunoglobulins_in_the_newborn"><img alt="Research paper thumbnail of Immunoglobulins in the newborn" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/48834417/Immunoglobulins_in_the_newborn">Immunoglobulins in the newborn</a></div><div class="wp-workCard_item"><span>Curr Opin Infect Dis</span><span>, 1991</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834417"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834417"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834417; 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ABSENCE OF THE THIRD COMPONENT OF COMPLEMENT Melvin Berger, MD, Ph.D., James E. Balow, MD, Cu...</span><a class="js-work-more-abstract" data-broccoli-component="work_strip.more_abstract" data-click-track="profile-work-strip-more-abstract" href="javascript:;"><span> more </span><span><i class="fa fa-caret-down"></i></span></a><span class="js-work-more-abstract-untruncated hidden">... ABSENCE OF THE THIRD COMPONENT OF COMPLEMENT Melvin Berger, MD, Ph.D., James E. Balow, MD, Curtis B. Wilson, MD, and Michael M. Frank, MD THE third component of complement (C3) is criti-cally involved in host defense and the mainte-nance of normal ...</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834415"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834415"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834415; window.Academia.workViewCountsFetcher.queue(workId, function (count) { var description = window.$h.commaizeInt(count) + " " + window.$h.pluralize(count, 'View'); $(".js-view-count[data-work-id=48834415]").text(description); 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</script> <div class="js-work-strip profile--work_container" data-work-id="48834414"><div class="profile--work_thumbnail hidden-xs"><a class="js-work-strip-work-link" data-click-track="profile-work-strip-thumbnail" rel="nofollow" href="https://www.academia.edu/48834414/_74_Third_component_of_human_complement_C3"><img alt="Research paper thumbnail of [74] Third component of human complement: C3" class="work-thumbnail" src="https://a.academia-assets.com/images/blank-paper.jpg" /></a></div><div class="wp-workCard wp-workCard_itemContainer"><div class="wp-workCard_item wp-workCard--title"><a class="js-work-strip-work-link text-gray-darker" data-click-track="profile-work-strip-title" rel="nofollow" href="https://www.academia.edu/48834414/_74_Third_component_of_human_complement_C3">[74] Third component of human complement: C3</a></div><div class="wp-workCard_item"><span>Methods in Enzymology</span><span>, 1990</span></div><div class="wp-workCard_item wp-workCard--actions"><span class="work-strip-bookmark-button-container"></span><span class="wp-workCard--action visible-if-viewed-by-owner inline-block" style="display: none;"><span class="js-profile-work-strip-edit-button-wrapper profile-work-strip-edit-button-wrapper" data-work-id="48834414"><a class="js-profile-work-strip-edit-button" tabindex="0"><span><i class="fa fa-pencil"></i></span><span>Edit</span></a></span></span></div><div class="wp-workCard_item wp-workCard--stats"><span><span><span class="js-view-count view-count u-mr2x" data-work-id="48834414"><i class="fa fa-spinner fa-spin"></i></span><script>$(function () { var workId = 48834414; 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