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Development of potency, breadth and resilience to viral escape mutations in SARS-CoV-2 neutralizing antibodies.

Authors :
Muecksch F
Weisblum Y
Barnes CO
Schmidt F
Schaefer-Babajew D
Lorenzi JCC
Flyak AI
DeLaitsch AT
Huey-Tubman KE
Hou S
Schiffer CA
Gaebler C
Wang Z
Da Silva J
Poston D
Finkin S
Cho A
Cipolla M
Oliveira TY
Millard KG
Ramos V
Gazumyan A
Rutkowska M
Caskey M
Nussenzweig MC
Bjorkman PJ
Hatziioannou T
Bieniasz PD
Source :
BioRxiv : the preprint server for biology [bioRxiv] 2021 Mar 08. Date of Electronic Publication: 2021 Mar 08.
Publication Year :
2021

Abstract

Antibodies elicited in response to infection undergo somatic mutation in germinal centers that can result in higher affinity for the cognate antigen. To determine the effects of somatic mutation on the properties of SARS-CoV-2 spike receptor-binding domain (RBD)-specific antibodies, we analyzed six independent antibody lineages. As well as increased neutralization potency, antibody evolution changed pathways for acquisition of resistance and, in some cases, restricted the range of neutralization escape options. For some antibodies, maturation apparently imposed a requirement for multiple spike mutations to enable escape. For certain antibody lineages, maturation enabled neutralization of circulating SARS-CoV-2 variants of concern and heterologous sarbecoviruses. Antibody-antigen structures revealed that these properties resulted from substitutions that allowed additional variability at the interface with the RBD. These findings suggest that increasing antibody diversity through prolonged or repeated antigen exposure may improve protection against diversifying SARS-CoV-2 populations, and perhaps against other pandemic threat coronaviruses.<br />Competing Interests: Declaration of Interests The Rockefeller University has filed provisional patent applications in connection with this work on which M.C.N. (US patent 63/021,387) and Y.W., F.S., T.H. and P.D.B. (US patent 63/036,124) are listed as inventors.

Details

Language :
English
ISSN :
2692-8205
Database :
MEDLINE
Journal :
BioRxiv : the preprint server for biology
Accession number :
33758864
Full Text :
https://doi.org/10.1101/2021.03.07.434227