Seattle BioMed, Seattle, Washington, USA.
PLoS Pathog. 2011 Jan 13;7(1):e1001251. doi: 10.1371/journal.ppat.1001251.
Recent cross-sectional analyses of HIV-1+ plasmas have indicated that broadly cross-reactive neutralizing antibody responses are developed by 10%-30% of HIV-1+ subjects. The timing of the initial development of such anti-viral responses is unknown. It is also unknown whether the emergence of these responses coincides with the appearance of antibody specificities to a single or multiple regions of the viral envelope glycoprotein (Env). Here we analyzed the cross-neutralizing antibody responses in longitudinal plasmas collected soon after and up to seven years after HIV-1 infection. We find that anti-HIV-1 cross-neutralizing antibody responses first become evident on average at 2.5 years and, in rare cases, as early as 1 year following infection. If cross-neutralizing antibody responses do not develop during the first 2-3 years of infection, they most likely will not do so subsequently. Our results indicate a potential link between the development of cross-neutralizing antibody responses and specific activation markers on T cells, and with plasma viremia levels. The earliest cross-neutralizing antibody response targets a limited number of Env regions, primarily the CD4-binding site and epitopes that are not present on monomeric Env, but on the virion-associated trimeric Env form. In contrast, the neutralizing activities of plasmas from subjects that did not develop cross-neutralizing antibody responses target epitopes on monomeric gp120 other than the CD4-BS. Our study provides information that is not only relevant to better understanding the interaction of the human immune system with HIV but may guide the development of effective immunization protocols. Since antibodies to complex epitopes that are present on the virion-associated envelope spike appear to be key components of earliest cross-neutralizing activities of HIV-1+ plasmas, then emphasis should be made to elicit similar antibodies by vaccination.
最近对 HIV-1+ 血浆的横断面分析表明,10%-30%的 HIV-1+ 个体产生了广泛交叉反应的中和抗体反应。这些抗病毒反应最初发展的时间尚不清楚。也不知道这些反应的出现是否与针对病毒包膜糖蛋白(Env)单一或多个区域的抗体特异性的出现相一致。在这里,我们分析了 HIV-1 感染后不久和长达 7 年内采集的纵向血浆中的交叉中和抗体反应。我们发现,抗 HIV-1 交叉中和抗体反应平均在感染后 2.5 年首次明显出现,在极少数情况下,早在感染后 1 年就出现。如果在感染的头 2-3 年内没有产生交叉中和抗体反应,那么它们随后很可能也不会产生。我们的研究结果表明,交叉中和抗体反应的发展与 T 细胞上特定的激活标记物以及与血浆病毒血症水平之间存在潜在联系。最早的交叉中和抗体反应针对Env 区域的有限数量,主要是 CD4 结合位点和单体 Env 上不存在的表位,但存在于病毒相关的三聚体 Env 形式上。相比之下,未产生交叉中和抗体反应的受试者的血浆中的中和活性针对除 CD4-BS 之外的单体 gp120 上的表位。我们的研究提供了不仅与更好地理解人类免疫系统与 HIV 的相互作用相关的信息,而且可能为有效的免疫接种方案的制定提供指导。由于针对病毒相关包膜刺突上存在的复杂表位的抗体似乎是 HIV-1+ 血浆中最早的交叉中和活性的关键组成部分,那么应该通过接种来强调引发类似抗体。