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Recapitulation of HIV-1 Env-Antibody Coevolution in Macaques Leading to Neutralization Breadth

Authors :
Shuyi Wang
Chengyan Zhao
Anya M. Bauer
Fang-Hua Lee
Cara W. Chao
Emily Lindemuth
Nicole A. Doria-Rose
Juliette Rando
Frederic Bibollet-Ruche
Kevin Wiehe
Mario Roederer
Chaim A. Schramm
Bette T. Korber
Donald D. Raymond
Kwan-Ki Hwang
Weimin Liu
George M. Shaw
Mark G. Lewis
Ronnie M. Russell
Hui Li
Stephen C. Harrison
Baoshan Zhang
Ryan S. Roark
Andrew G. Smith
Jesse Connell
Kevin O. Saunders
Hui Geng
Alexander I. Murphy
Mattia Bonsignori
Elena E. Giorgi
Maho Okumura
Hema Chug
Beatrice H. Hahn
John R. Mascola
Peter D. Kwong
Peter T. Hraber
Christina Rosario
Jessica G. Smith
David R. Ambrozak
Yu Ding
Wenge Ding
Richard Nguyen
Rosemarie D. Mason
Barton F. Haynes
Mark K. Louder
Daniel C. Douek
Kshitij Wagh
Jason Gorman
Bob C. Lin
Thomas B. Kepler
Wilton B. Williams
Neha Chohan
Garnett Kelsoe
Gwo-Yu Chuang
Julia DeVoto
Katharine J. Bar
M. Anthony Moody
Source :
Science
Publication Year :
2020
Publisher :
Cold Spring Harbor Laboratory, 2020.

Abstract

Convergent HIV evolution across species Human immunodeficiency virus (HIV) has a highly diverse envelope protein that it uses to target human cells, and the complexity of the viral envelope has stymied vaccine development. Roark et al. report that the immediate and short-term evolutionary potential of the HIV envelope is constrained because of a number of essential functions, including antibody escape. Consequently, when introduced into humans as HIV or into rhesus macaque monkeys as chimeric simian-human immunodeficiency virus, homologous envelope glycoproteins appear to exhibit conserved patterns of sequence evolution, in some cases eliciting broadly neutralizing antibodies in both hosts. Conserved patterns of envelope variation and homologous B cell responses in humans and monkeys represent examples of convergent evolution that may serve to guide HIV vaccine development. Science , this issue p. eabd2638

Details

Database :
OpenAIRE
Journal :
Science
Accession number :
edsair.doi.dedup.....4ed080ccce387e2255c23bd3823a0579