Institut de recerca de la SIDA IrsiCaixa-HIVACAT, Institut d'Investigació en Ciències de la Salut Germans Trias I Pujol, Badalona, Spain.
AIDS. 2013 Jun 1;27(9):1375-85. doi: 10.1097/QAD.0b013e32835fac08.
Susceptibility to HIV transmission by sexual intercourse has been associated with cellular anti-HIV responses. We aimed to also evaluate potential systemic humoral responses against HIV in a group of HIV-exposed seronegative individuals (HESN) in stable relationship with HIV-infected partners.
We recruited 27 serodiscordant couples. HESN were classified according to HIV exposure into very low/low and moderate/high risk. Plasma from HESN and HIV partners were tested for neutralizing capacity and for the recognition of cell-surface expressed and recombinant forms of HIV envelope glycoproteins (Env). Healthy individuals (healthy control, n=11) were used as controls.
Recognition of cell-surface expressed Env by both immunoglobulin (Ig)G and IgA was higher in plasma samples from HESN than in healthy controls (P=0.0062 and P=0.0144, respectively). IgG binding to Env was significantly increased in HESN after unmasking CD4-induced epitopes (P=0.001), suggesting a wide range of targeted epitopes. Remarkably, ELISA assays using trimeric gp140 or monomeric gp120 failed to detect significant differences in reactivity between groups. Neutralization analysis showed residual activity in only three HESN samples (11%), whereas 70% of HIV-infected partners showed neutralizing activity. Although anti-Env humoral responses were found in 85% of HESN, their magnitude was not associated with the estimated level of exposure or the detection of HIV-specific cellular immune responses.
A high proportion of HESN show detectable plasma IgG or IgA recognizing different exposed and cryptic Env native epitopes unrelated to neutralizing capacity. Therefore, low but persistent HIV exposure induces new virus-specific systemic humoral responses or boosts preexisting natural antibodies.
性传播感染 HIV 的易感性与细胞抗 HIV 反应有关。我们旨在评估一组与 HIV 感染伴侣稳定关系的 HIV 暴露血清阴性个体 (HESN) 中针对 HIV 的潜在系统体液反应。
我们招募了 27 对血清不一致的夫妇。HESN 根据 HIV 暴露情况分为低/极低风险和中/高风险。检测 HESN 和 HIV 伴侣血浆的中和能力以及对细胞表面表达和重组 HIV 包膜糖蛋白 (Env) 的识别。健康个体(健康对照组,n=11)作为对照。
与健康对照组相比,HESN 血浆样本中 IgG 和 IgA 识别细胞表面表达的 Env 的能力更高(P=0.0062 和 P=0.0144)。在未掩蔽 CD4 诱导的表位后,HESN 中 IgG 与 Env 的结合显著增加(P=0.001),表明存在广泛的靶向表位。值得注意的是,使用三聚体 gp140 或单体 gp120 的 ELISA 检测未能检测到各组之间反应性的显著差异。中和分析仅在三个 HESN 样本(11%)中显示出残留活性,而 70%的 HIV 感染伴侣显示出中和活性。尽管 85%的 HESN 中存在抗 Env 体液反应,但它们的幅度与估计的暴露水平或 HIV 特异性细胞免疫反应的检测无关。
很大一部分 HESN 可检测到识别不同暴露和隐匿性 Env 天然表位的血浆 IgG 或 IgA,与中和能力无关。因此,低但持续的 HIV 暴露会诱导新的病毒特异性系统性体液反应或增强先前存在的天然抗体。