Antibody‐mediated control mechanisms of viral infections

Author:

Mackin Samantha R.12,Sariol Alan1,Diamond Michael S.12345ORCID

Affiliation:

1. Department of Medicine Washington University School of Medicine St. Louis Missouri USA

2. Department of Pathology & Immunology and Center for Genome Sciences, Lab & Genomic Medicine Washington University School of Medicine St. Louis Missouri USA

3. Department of Molecular Microbiology Washington University School of Medicine St. Louis Missouri USA

4. Andrew M. and Jane M. Bursky the Center for Human Immunology and Immunotherapy Programs Washington University School of Medicine St. Louis Missouri USA

5. Center for Vaccines and Immunity to Microbial Pathogens Washington University School of Medicine St. Louis Missouri USA

Abstract

SummaryAntibodies generated after vaccination or natural pathogen exposure are essential mediators of protection against many infections. Most studies with viruses have focused on antibody neutralization, in which protection is conferred by the fragment antigen binding region (Fab) through targeting of different steps in the viral lifecycle including attachment, internalization, fusion, and egress. Beyond neutralization, the fragment crystallizable (Fc) region of antibodies can integrate innate and adaptive immune responses by engaging complement components and distinct Fc gamma receptors (FcγR) on different host immune cells. In this review, we discuss recent advances in our understanding of antibody neutralization and Fc effector functions, and the assays used to measure them. Additionally, we describe the contexts in which these mechanisms are associated with protection against viruses and highlight how Fc‐FcγR interactions can improve the potency of antibody‐based therapies.

Funder

Division of Microbiology and Infectious Diseases

Publisher

Wiley

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