Wu Lan, Yang Zhi-Yong, Xu Ling, Welcher Brent, Winfrey Sarah, Shao Yiming, Mascola John R, Nabel Gary J
Vaccine Research Center, NIAID, National Institutes of Health, Room 4502, Bldg. 40, MSC-3005, 40 Convent Drive, Bethesda, MD 20892-3005, USA.
Vaccine. 2006 Jun 5;24(23):4995-5002. doi: 10.1016/j.vaccine.2006.03.083. Epub 2006 Apr 18.
To understand the cross-reactivity of antibodies directed against variable regions of human immunodeficiency virus-1 (HIV-1) envelope (Env), chimeric immunogens were prepared from different clades with modifications in variable regions, and the resulting neutralizing antibody response was evaluated. The V3-specific neutralization activity induced by a clade B immunogen was limited to clade B viruses and was blocked by a clade B V3 peptide, but not by analogous clade A or C V3 peptides. In contrast, the V3 response elicited by a clade C immunogen cross-reacted with sensitive clade B viruses. The V3 region from a clade C virus, when introduced into a clade B sequence, elicited cross-clade activity, which could be reversed by V3 peptides derived from clades A and C. Thus, the anti-V3 antibody response elicited by a clade C immunogen could cross-react with heterologous clade viruses. Additionally, we describe a V1-specific immune response that mediated neutralization limited to the homologous HIV IIIB isolate and may be partially responsible for the commonly observed strain-specific neutralization responses elicited by vaccine immunogens.
为了解针对人类免疫缺陷病毒1型(HIV-1)包膜(Env)可变区的抗体的交叉反应性,制备了来自不同分支且可变区有修饰的嵌合免疫原,并评估了由此产生的中和抗体反应。B分支免疫原诱导的V3特异性中和活性仅限于B分支病毒,可被B分支V3肽阻断,但不能被A或C分支的类似V3肽阻断。相比之下,C分支免疫原引发的V3反应与敏感的B分支病毒发生交叉反应。将C分支病毒的V3区引入B分支序列时,会引发跨分支活性,这种活性可被A和C分支的V3肽逆转。因此,C分支免疫原引发的抗V3抗体反应可与异源分支病毒发生交叉反应。此外,我们描述了一种V1特异性免疫反应,该反应介导的中和作用仅限于同源的HIV IIIB分离株,可能部分解释了疫苗免疫原引发的常见的毒株特异性中和反应。