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An HIV Vaccine Targeting the V2 Region of the HIV Envelope Induces a Highly Durable Polyfunctional Fc-Mediated Antibody Response in Rhesus Macaques
Author(s) -
Rebecca Powell,
Svenja Weiß,
Alisa Fox,
Xiaomei Liu,
Vincenza Itri,
Xunqing Jiang,
Christina C. Luo,
David A. Spencer,
Shilpi Pandey,
Tracy Cheever,
Deborah H. Fuller,
Maxim Totrov,
Ann J. Hessell,
Nancy L. Haigwood,
XiangPeng Kong,
Susan ZollaPazner
Publication year - 2020
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.01175-20
Subject(s) - hiv vaccine , virology , aids vaccines , biology , human immunodeficiency virus (hiv) , immunology , vaccine efficacy , antibody , lentivirus , antibody response , vaccine trial , simian immunodeficiency virus , vaccination , viral disease
The only HIV vaccine trial for which protective efficacy was detected correlated this efficacy with V2-specific Abs that were effectively nonneutralizing. This result has fueled a decade of HIV vaccine research focused on designing an HIV vaccine capable of eliciting V2-focused, polyfunctional Abs that effectively bind HIV and trigger various leukocytes to kill the virus and restrict viral spread. From the numerous vaccine candidates designed and tested as part of our V2-focused preclinical vaccine program, we have identified immunogens and a vaccine regimen that induces a highly durable and polyfunctional V2-focused Ab response in rhesus macaques, described herein.

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