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For this goal, molecular vaccines against other virus protein(s), as for instance, against gene, coding virus membrane (M) protein or against virus gene, coding viral envelope (E) protein, but also specific siRNAs against the virus gene, coding viral Spike (S) protein, should be developed and tested. Additionally, taking in consideration the eventual changes in many physical and chemical properties of the viral particle after its connection with respective generated antibodies against any of the mentioned proteins, probability for connection of the virion with the cellular receptor by viral S protein would eventually also be prevented. In this connection, the main idea is directed to application of strategies of priming with molecular vaccine against any of the viral genes, coding the mentioned above proteins, and boosting with specific siRNAs against virus gene, coding viral S protein. Both siRNAs and molecular vaccines should be constructed and applied by ways, by which maximal safety for the cell and the organism to be achieved. So, in vitro-incubated cells should be inoculated with viral strain with RNA-genome (if is possible, belonging to Coronaviridae family), which should then be treated with appropriate siRNAs against the virus gene, coding viral S protein, necessary about viral penetration in the cell. Molecular vaccines against other virus protein(s) should also be designed. Subsequent evaluation on the in vivo-influence of the tested siRNAs against virus S protein and molecular vaccines against other viral protein(s) on appropriate experimental animals, both non-infected and previously infected with the same RNA-viral strain, should be performed. After performance of all steps, evaluation on the in vivo-influence of the tested siRNAs against virus S protein and molecular vaccines against other viral protein(s) on appropriate immunodeficiency rodents as NOD or SCID mice is necessary, among which should also be available sub-groups, previously infected with the same RNA-virus strain"> <meta name="citation_abstract_html_url" content="https://hindi.pulsus.com/abstract/development-of-new-strategies-against-sars-cov2covid19-10307.html"> </head> <body> <header class="m-b-0"> <div class="container py-3 d-none d-lg-block"> <div class="row justify-content-between"> <div class="col-12 col-sm-4 col-md-3"> <a href="https://hindi.pulsus.com/" title="पल्सस ग्रुप"> <img alt="पल्सस ग्रुप" src="/images/pulsus-logo-red.svg" class="img-fluid"></a> </div> <div class="col-12 col-sm-8 my-4 my-sm-0 top_img_head"> <a href="https://hindi.pulsus.com/submit-manuscript.html"><img alt="पल्सस ग्रुप" src="/images/80.jpg" class="img-fluid float-right" /> 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For this goal, molecular vaccines against other virus protein(s), as for instance, against gene, coding virus membrane (M) protein or against virus gene, coding viral envelope (E) protein, but also specific siRNAs against the virus gene, coding viral Spike (S) protein, should be developed and tested. Additionally, taking in consideration the eventual changes in many physical and chemical properties of the viral particle after its connection with respective generated antibodies against any of the mentioned proteins, probability for connection of the virion with the cellular receptor by viral S protein would eventually also be prevented. In this connection, the main idea is directed to application of strategies of priming with molecular vaccine against any of the viral genes, coding the mentioned above proteins, and boosting with specific siRNAs against virus gene, coding viral S protein. Both siRNAs and molecular vaccines should be constructed and applied by ways, by which maximal safety for the cell and the organism to be achieved. So, in vitro-incubated cells should be inoculated with viral strain with RNA-genome (if is possible, belonging to Coronaviridae family), which should then be treated with appropriate siRNAs against the virus gene, coding viral S protein, necessary about viral penetration in the cell. Molecular vaccines against other virus protein(s) should also be designed. Subsequent evaluation on the in vivo-influence of the tested siRNAs against virus S protein and molecular vaccines against other viral protein(s) on appropriate experimental animals, both non-infected and previously infected with the same RNA-viral strain, should be performed. After performance of all steps, evaluation on the in vivo-influence of the tested siRNAs against virus S protein and molecular vaccines against other viral protein(s) on appropriate immunodeficiency rodents as NOD or SCID mice is necessary, among which should also be available sub-groups, previously infected with the same RNA-virus strain</p> <div class="alert alert-info text-left"><b>अस्वीकृति:</b> इस सारांश का अनुवाद कृत्रिम बुद्धिमत्ता उपकरणों का उपयोग करके किया गया है और इसे अभी तक समीक्षा या सत्यापित नहीं किया गया है।</div> </div>  <div class="col-md-2"><ul class="sidebar-soc"> <li><a class="soc-twitter" href="https://twitter.com/pulsus5" target="_blank"><i class="fa fa-twitter" aria-hidden="true"></i></a></li> <li><a class="soc-linkedin" href="https://www.linkedin.com/company/pulsus-journals" target="_blank"><i aria-hidden="true" class="fa fa-linkedin"></i></a></li> </ul> <div> </div> <div class="card shadow-sm sidebar mb-3"> <h4 class="card-header pr-0" style="padding:6px 0px 6px 7px; 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