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10.3390/v13061037

http://scihub22266oqcxt.onion/10.3390/v13061037
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34072720!8226613!34072720
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suck abstract from ncbi


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pmid34072720      Viruses 2021 ; 13 (6): ä
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  • Requirement of Fc-Fc Gamma Receptor Interaction for Antibody-Based Protection against Emerging Virus Infections #MMPMID34072720
  • Keeler SP; Fox JM
  • Viruses 2021[May]; 13 (6): ä PMID34072720show ga
  • Identification of therapeutics against emerging and re-emerging viruses remains a continued priority that is only reinforced by the recent SARS-CoV-2 pandemic. Advances in monoclonal antibody (mAb) isolation, characterization, and production make it a viable option for rapid treatment development. While mAbs are traditionally screened and selected based on potency of neutralization in vitro, it is clear that additional factors contribute to the in vivo efficacy of a mAb beyond viral neutralization. These factors include interactions with Fc receptors (FcRs) and complement that can enhance neutralization, clearance of infected cells, opsonization of virions, and modulation of the innate and adaptive immune response. In this review, we discuss recent studies, primarily using mouse models, that identified a role for Fc-FcgammaR interactions for optimal antibody-based protection against emerging and re-emerging virus infections.
  • |Animals[MESH]
  • |Antibodies, Monoclonal/immunology/therapeutic use[MESH]
  • |Antibodies, Neutralizing/immunology/therapeutic use[MESH]
  • |Antibody-Dependent Cell Cytotoxicity[MESH]
  • |Communicable Diseases, Emerging/*immunology/therapy/virology[MESH]
  • |Humans[MESH]
  • |Immunization, Passive[MESH]
  • |Immunoglobulin Fc Fragments/*immunology[MESH]
  • |Phagocytosis[MESH]
  • |Receptors, IgG/*immunology[MESH]
  • |Virus Diseases/*immunology/therapy/virology[MESH]


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