Vaccine-induced Env V1-V2 IgG3 correlates with lower HIV-1 infection risk and declines soon after vaccination.

Vaccine-induced Env V1-V2 IgG3 correlates with lower HIV-1 infection risk and declines soon after vaccination.
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疫苗诱导的ENV V1-V2 IgG3与HIV-1感染风险较低相关,并在疫苗接种后不久下降。

DOI:
10.1126/scitranslmed.3007730
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发表时间:
2014-03-19
影响因子:
17.1
通讯作者:
Tomaras GD
Tomaras GD
中科院分区:
医学1区
文献类型:
--
作者:
Yates NL;Liao HX;Fong Y;deCamp A;Vandergrift NA;Williams WT;Alam SM;Ferrari G;Yang ZY;Seaton KE;Berman PW;Alpert MD;Evans DT;O'Connell RJ;Francis D;Sinangil F;Lee C;Nitayaphan S;Rerks-Ngarm S;Kaewkungwal J;Pitisuttithum P;Tartaglia J;Pinter A;Zolla-Pazner S;Gilbert PB;Nabel GJ;Michael NL;Kim JH;Montefiori DC;Haynes BF;Tomaras GD

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HIV-1–specific immunoglobulin G (IgG) subclass antibodies bind to distinct cellular Fc receptors. Antibodies of the same epitope specificity but of a different subclass therefore can have different antibody effector functions. The study of IgG subclass profiles between different vaccine regimens used in clinical trials with divergent efficacy outcomes can provide information on the quality of the vaccine-induced B cell response. We show that HIV-1–specific IgG3 distinguished two HIV-1 vaccine efficacy studies (RV144 and VAX003 clinical trials) and correlated with decreased risk of HIV-1 infection in a blinded follow-up case-control study with the RV144 vaccine. HIV-1–specific IgG3 responses were not long-lived, which was consistent with the waning efficacy of the RV144 vaccine. These data suggest that specific vaccine-induced HIV-1 IgG3 should be tested in future studies of immune correlates in HIV-1 vaccine efficacy trials.
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