Vaccination induces HIV broadly neutralizing antibody precursors in humans

Broadly neutralizing antibodies (bnAbs) can protect against HIV infection but have not been induced by human vaccination. A key barrier to bnAb induction is vaccine priming of rare bnAb-precursor B cells. In a randomized, double-blind, placebo-controlled phase 1 clinical trial, the HIV vaccine-primi...

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Veröffentlicht in:Science (American Association for the Advancement of Science) 2022-12, Vol.378 (6623), p.eadd6502-eadd6502
Hauptverfasser: Leggat, David J, Cohen, Kristen W, Willis, Jordan R, Fulp, William J, deCamp, Allan C, Kalyuzhniy, Oleksandr, Cottrell, Christopher A, Menis, Sergey, Finak, Greg, Ballweber-Fleming, Lamar, Srikanth, Abhinaya, Plyler, Jason R, Schiffner, Torben, Liguori, Alessia, Rahaman, Farhad, Lombardo, Angela, Philiponis, Vincent, Whaley, Rachael E, Seese, Aaron, Brand, Joshua, Ruppel, Alexis M, Hoyland, Wesley, Yates, Nicole L, Williams, LaTonya D, Greene, Kelli, Gao, Hongmei, Mahoney, Celia R, Corcoran, Martin M, Cagigi, Alberto, Taylor, Alison, Brown, David M, Ambrozak, David R, Sincomb, Troy, Hu, Xiaozhen, Tingle, Ryan, Georgeson, Erik, Eskandarzadeh, Saman, Alavi, Nushin, Lu, Danny, Mullen, Tina-Marie, Kubitz, Michael, Groschel, Bettina, Maenza, Janine, Kolokythas, Orpheus, Khati, Nadia, Bethony, Jeffrey, Crotty, Shane, Roederer, Mario, Karlsson Hedestam, Gunilla B, Tomaras, Georgia D, Montefiori, David, Diemert, David, Koup, Richard A, Laufer, Dagna S, McElrath, M Juliana, McDermott, Adrian B, Schief, William R
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Sprache:eng
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Zusammenfassung:Broadly neutralizing antibodies (bnAbs) can protect against HIV infection but have not been induced by human vaccination. A key barrier to bnAb induction is vaccine priming of rare bnAb-precursor B cells. In a randomized, double-blind, placebo-controlled phase 1 clinical trial, the HIV vaccine-priming candidate eOD-GT8 60mer adjuvanted with AS01 had a favorable safety profile and induced VRC01-class bnAb precursors in 97% of vaccine recipients with median frequencies reaching 0.1% among immunoglobulin G B cells in blood. bnAb precursors shared properties with bnAbs and gained somatic hypermutation and affinity with the boost. The results establish clinical proof of concept for germline-targeting vaccine priming, support development of boosting regimens to induce bnAbs, and encourage application of the germline-targeting strategy to other targets in HIV and other pathogens.
ISSN:0036-8075
1095-9203
1095-9203
DOI:10.1126/science.add6502