Broliden P A, von Gegerfelt A, Clapham P, Rosen J, Fenyö E M, Wahren B, Broliden K
Department of Virology, National Bacteriological Laboratory, Stockholm, Sweden.
Proc Natl Acad Sci U S A. 1992 Jan 15;89(2):461-5. doi: 10.1073/pnas.89.2.461.
Four major neutralizing regions of the human immunodeficiency virus type 1 (HIV-1) envelope glycoprotein were identified and characterized with a panel of 80 HIV-1 antibody-positive human sera. Levels of neutralizing antibodies against the HIV-1 strains IIIB, SF2, and RF were compared with reactivity in ELISAs against peptides that correspond to certain regions of the HIV-1 envelope. A correlation between high neutralizing activity and strong seroreactivity against specific peptides suggested that the corresponding regions might be involved in neutralization. This was further substantiated by using peptides to inhibit neutralization by a panel of 10 HIV-1 antibody-positive sera. The positions of three neutralizing sites, defined earlier mostly by antisera from animals, were confirmed in the present study. Human sera thus recognize the strain-specific third variable region of gp120 (amino acids 304-318), the C-terminal end of gp120 (amino acids 489-508), and the conserved region in the intracellular part of gp41 (amino acids 732-746). It is likely that these different regions mediate help rather than self-sufficient neutralization. Furthermore, a human neutralizing region was detected in a conserved part of gp41 (amino acids 647-671). Accordingly, neutralizing antibodies directed to this region were found to be cross-reactive between HIV-1 strains. Peptides corresponding to these four regions were able to inhibit neutralization mediated by serum from HIV-1 antibody-positive individuals. These results indicate that this conserved B-cell epitope of the HIV-1 envelope elicits a virus-neutralizing antibody response during natural infection in humans and may therefore be considered for inclusion in a vaccine against HIV-1.
利用一组80份HIV-1抗体阳性的人血清,鉴定并表征了1型人类免疫缺陷病毒(HIV-1)包膜糖蛋白的四个主要中和区域。将针对HIV-1毒株IIIB、SF2和RF的中和抗体水平与针对对应于HIV-1包膜某些区域的肽的ELISA反应性进行了比较。高中和活性与针对特定肽的强血清反应性之间的相关性表明相应区域可能参与中和作用。通过使用肽抑制一组10份HIV-1抗体阳性血清的中和作用,进一步证实了这一点。本研究证实了先前主要由动物抗血清确定的三个中和位点的位置。人血清因此识别gp120的毒株特异性第三个可变区(氨基酸304 - 318)、gp120的C末端(氨基酸489 - 508)以及gp41细胞内部分的保守区(氨基酸732 - 746)。很可能这些不同区域介导辅助作用而非自身充分的中和作用。此外,在gp41的一个保守部分(氨基酸647 - 671)检测到一个人中和区域。因此,发现针对该区域的中和抗体在HIV-1毒株之间具有交叉反应性。对应于这四个区域的肽能够抑制HIV-1抗体阳性个体血清介导的中和作用。这些结果表明,HIV-1包膜的这个保守B细胞表位在人类自然感染期间引发病毒中和抗体反应,因此可考虑将其纳入抗HIV-1疫苗。