HLA Transgenic Mice based SIAT® Immunogenicity Assessment Service

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However, many small animal models cannot accurately predict human response due to their different genetic backgrounds and cannot eliminate the influence of species specificity on preclinical research, so many preclinical animal experimental results are very different from the human clinical response. </p> <p> Some studies have shown that major histocompatibility complex (MHC) plays important roles in biological defense system by expressing a variety of antigen peptides and inducing T cell immune response, and the genetic difference of MHC molecules among species is one of the important factors leading to this difference. Therefore, it can be considered to replace animal MHC molecules with human leukocyte antigen (HLA) molecules in the experimental animals, so as to effectively improve the accuracy of animal models in predicting human immune response. <strong>Creative Biolabs</strong> makes full use of this difference and cooperates with partners to develop the HLA transgenic mouse model. With the unique SIAT® platform, we can provide a one-stop <em>in vivo</em> immunogenicity analysis service. </p> <p class="ServiceShowPic"> <img loading="lazy" src="static/img/SIAT-Immunologic-Analysis-in-HLA-Transgenic-Mice-1.png" width="600" height="200" alt="Immunogenicity assessment workflow." /> Fig.1 Immunogenicity assessment workflow. </p> <h2 class="h2_tit page_tab_margin" id="tab1"> Background of HLA Transgenic Mice Progress </h2> <p> T cell receptors (TCRs) are the antigen recognition mechanism on the surface of T lymphocyte. TCR forms homologous interactions with antigens through MHC in mice, human HLA on the surface of somatic cells, and specialized antigen-presenting cells of the innate immune system. TCR recognition activates the downstream immune response, which produces strong adaptive immunity. </p> <p> The transplantation of HLA into immunocompromised mice is an important new tool for understanding human-specific pathogens and their immune responses. Using the mouse model, we can find the specific haplotype T cell epitope, which provides a powerful evaluation method for immunogenicity analysis. </p> <p class="ServiceShowPic"> <img loading="lazy" src="static/img/SIAT-Immunologic-Analysis-in-HLA-Transgenic-Mice-2.png" width="600" height="220" alt="Genetic humanization of individual targets or of entire portions of the immune system." /> Fig.2 Genetic humanization of individual targets or of entire portions of the immune system. (Zitvogel, 2016) </p> <h2 class="h2_tit page_tab_margin" id="tab2"> HLA Transgenic Mice in Immunologic Analysis </h2> <p> Immunologic analysis in HLA transgenic mice as the most important step in the immunogenicity test, a large amount of literature research and information retrieval are needed in the early stage. This model that can replicate human antigen presentation with HLA epitope binding specificity will continue to be used in more and more ways. Traditional vaccine methods, including epitope identification and validation, have been extended to cancer vaccine research. The evaluation of the antitumor activity of the tumor vaccine can be carried out directly in HLA transgenic mice. In T cell immunotherapy, HLA transgenic mice have been used to identify the sequence of high-affinity TCR, so as to develop a new chimeric antigen receptor (CAR) T-cell therapy. With the increase of immunotherapy research, these tools will become more and more important. </p> <p> In addition, an experiment has been applied to the evaluation of HLA transgenic mice to Graves' disease. Scientists combined the histocompatibility complex binding test with the immune and tolerance induction test of HLA transgenic mice to prepare epitopes (antigen processing independent epitopes) from the thyroid-stimulating hormone receptor (TSHR). When the HLA transgenic mice were injected, the mixture of two immunodominant epitopes was sufficient to inhibit the response of T cells and antibodies to TSHR without damaging the tolerance of the mice. </p> <p> In terms of immunologic analysis, <strong>Creative Biolabs</strong> has rich experimental experience and advanced technology. If you have any requirements, please <a class="inquiry-button">contact us</a>. </p> <h2 class="h2_tit page_tab_margin" id="tab3"> Published Data </h2> <ul class="ullist"> <li> <strong>Vaccine's Ability Assessment by HLA Transgenic Mice</strong> </li> </ul> <p class="show-center"> <img loading="lazy" src="static/img/1-2-8-1-4-1-immunologic-analysis-in-hla-transgenic-mice-3.jpg" width="300" height="243" alt="" />Fig. 3 Virus-specific antibody responses elicited in vaccinated HLA-DR3 mice. (Callie E. Bounds, 2017) </p> <p> The research described in the article demonstrates the utility of an immunoinformatics-derived DNA vaccine encoding class II T cell epitopes from various viruses, which proved immunogenic in HLA transgenic mice. This study underscores the potential for using HLA transgenic mice to evaluate the immunogenicity of vaccines designed based on human immune responses, thereby bridging a crucial gap between preclinical studies and human trials. HLA transgenic mice were crucial for confirming the vaccine's ability to induce a human-like immune response, notably demonstrating significant cellular and humoral responses upon vaccination. This model system is particularly valuable for assessing vaccine efficacy before clinical trials, highlighting its role in preclinical vaccine development. </p> <div class="reference"> <strong>References</strong> <ol class="ollist decimal"> <li> Zitvogel, L.; <em>et al</em>. Mouse models in oncoimmunology. <em>Nature Reviews Cancer. </em>2016, 16: 759-773. </li> <li> Bounds, Callie E., et al. "An immunoinformatics-derived DNA vaccine encoding human class II T cell epitopes of Ebola virus, Sudan virus, and Venezuelan equine encephalitis virus is immunogenic in HLA transgenic mice."<em>Human vaccines & immunotherapeutics</em>13.12 (2017): 2824-2836. </li> </ol> </div> <script type="text/javascript"> window.addEventListener('load',function(){ faqlist(4); }); </script> <h2 class="h2_tit page_tab_margin" id="tab4"> FAQ </h2> <ol class="ollist faqlist"> <li> <span class="sFAQTit">What is the purpose of using HLA transgenic mice in immunogenicity assessment?</span> <p> HLA transgenic mice are utilized to evaluate the immunogenicity of biotherapeutics and vaccines. By expressing human leukocyte antigen (HLA) molecules, these mice provide a model that more closely mimics the human immune response, enabling researchers to predict potential immunogenic reactions in humans more accurately. </p> </li> <li> <span class="sFAQTit">How do HLA transgenic mice differ from normal mice in immunogenicity studies?</span> <p> Unlike standard mice, HLA transgenic mice are genetically modified to express specific HLA molecules that are found in humans. This modification allows them to present peptides and proteins in a way that mimics human immune mechanisms, offering more relevant data on how a drug might interact with the human immune system. </p> </li> <li> <span class="sFAQTit">What types of HLA alleles are typically used in these transgenic models?</span> <p> Common HLA alleles used in transgenic models include HLA-DR, HLA-DQ, and HLA-A2 among others. These alleles are selected based on their prevalence in the human population and their known roles in drug-related immune responses, ensuring broad applicability of the results. </p> </li> <li> <span class="sFAQTit">Can HLA transgenic mice predict all types of immune responses?</span> <p> While HLA transgenic mice are excellent tools for predicting T-cell mediated immune responses due to their expression of human HLA molecules, they may not fully predict other immune responses, such as those mediated by antibodies or innate immune cells. Combining their use with other models can provide a comprehensive immunogenicity assessment. </p> </li> <li> <span class="sFAQTit">What are the limitations of using HLA transgenic mice for immunogenicity testing?</span> <p> One limitation is that while they express human HLA molecules, other aspects of their immune system remain murine. This can affect the interaction between cells and cytokines, potentially leading to differences in immune response compared to humans. Additionally, these models can be expensive and require specialized breeding and handling. </p> </li> <li> <span class="sFAQTit">How are HLA transgenic mice developed?</span> <p> These mice are developed through genetic engineering techniques where genes encoding human HLA molecules are inserted into the mouse genome. This process often involves the use of vectors and promoters to ensure the correct expression of the HLA genes in appropriate tissues. </p> </li> <li> <span class="sFAQTit">What kind of studies typically use HLA transgenic mice?</span> <p> These mice are primarily used in preclinical studies to assess the immunogenic potential of therapeutic proteins, vaccines, and other biologics. Their use is crucial in drug development for autoimmune diseases, cancer, and infectious diseases where immune response plays a significant role. </p> </li> <li> <span class="sFAQTit">How do the results from HLA transgenic mice impact drug development?</span> <p> Results from studies using HLA transgenic mice can significantly influence the development pathway of a biotherapeutic. Data on immunogenicity can lead to modifications in the drug's molecular structure, dosing regimens, or delivery methods to minimize adverse immune reactions in humans. </p> </li> </ol> <h2 class="h2_tit page_tab_margin" id="tab5"> Resources </h2> <p> Use the resources in our library to help you understand your options and make critical decisions for your study. </p> <div class="tab_nav"> <span class="tab_choosebg">Videos</span><span>Articles</span> </div>  <div class="tab_cont" style="display:block;"> <div class="row pagerow_pt"> <div class="col-md-4"> <div class="pagerow_pt_unit"> <img loading="lazy" src="../static/img/immunogenicity-overview-of-therapeutic-biologics.jpg" alt="" /> </div> <a href="https://youtu.be/J430752_dTo" target="_blank">Immunogenicity overview of therapeutic biologics</a> </div> </div> </div>  <div class="tab_cont"> <div class="row pagerow_pt"> <div class="col-md-4"> <div class="pagerow_pt_unit_2"> <img loading="lazy" src="static/img/4-2-14-immune-monitoring-for-immunogenicity-assessment-1.jpg" alt="" /> </div> <a href="/immune-monitoring-for-immunogenicity-assessment.html">Immune Monitoring for Immunogenicity Assessment</a> </div> <div class="col-md-4"> <div class="pagerow_pt_unit_2"> <img loading="lazy" src="static/img/4-2-14-current-immunogenicity-evaluation-systems-a-deep-dive-by-creative-biolabs-1.jpg" alt="" /> </div> <a href="/current-immunogenicity-evaluation-systems.html">Current Immunogenicity Evaluation Systems: A Deep Dive by Creative Biolabs</a> </div> <div class="col-md-4"> <div class="pagerow_pt_unit_2"> <img loading="lazy" src="static/img/4-2-14-1-in-silico-immunogenicity-assessment-the-leading-edge-approach-to-drug-development-1.jpg" alt="" /> </div> <a href="/in-silico-immunogenicity-assessment-the-leading-edge-approach-to-drug-development.html"><i>In Silico</i> Immunogenicity Assessment: The Leading-edge Approach to Drug Development</a> </div> <div class="col-md-4"> <div class="pagerow_pt_unit_2"> <img loading="lazy" src="static/img/4-2-14-4-how-to-evaluate-the-immunogenicity-of-therapeutic-protein-drugs-in-vivo-1.jpg" alt="" /> </div> <a href="/how-to-evaluate-the-immunogenicity-of-therapeutic-protein-drugs-in-vivo.html">How to Evaluate the Immunogenicity of Therapeutic Protein Drugs <i>In Vivo</i></a> </div> <div class="col-md-4"> <div class="pagerow_pt_unit_2"> <img loading="lazy" src="static/img/4-2-14-5-the-origin-and-detection-methods-of-anti-drug-antibodies-1.jpg" alt="" /> </div> <a href="/the-origin-and-detection-methods-of-anti-drug-antibodies.html">The Origin and Detection Methods of Anti-Drug Antibodies</a> </div> <div class="col-md-4"> <div class="pagerow_pt_unit_2"> <img loading="lazy" src="static/img/4-2-14-1-8-immunogenic-risk-assessment-of-therapeutic-proteins-1.jpg" alt="" /> </div> <a href="/immunogenic-risk-assessment-of-therapeutic-proteins.html">Immunogenic Risk Assessment of Therapeutic Proteins</a> </div> <div class="col-md-4"> <div class="pagerow_pt_unit_2"> <img loading="lazy" src="static/img/anti-drug-antibody-introduction-1.jpg" alt="" /> </div> <a href="/anti-drug-antibody-introduction.html">Anti-Drug Antibody Introduction</a> </div> </div> </div> <script> window.addEventListener('load',function(){ // $(function () { $(".tab_nav span").click(function(){ var eqindex=$(this).index(); $(this).addClass("tab_choosebg"); $(this).siblings("span").removeClass("tab_choosebg"); $(".tab_cont").hide().eq(eqindex).show(); }) // }) }); </script><br> <p class="pronote"><i class="fa fa-exclamation-triangle"></i>All listed services and products are For Research Use Only. 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