Chen Y H, Dierich M P
Department of Biology, Tsinghua University, china.
Immunol Lett. 1996 Sep;52(2-3):153-6. doi: 10.1016/0165-2478(96)02603-x.
Previous studies by us and others showed that HIV-1 gp41 by the immunosuppressive domain (amino acids 583-599) could bind to human T, B and monocytic cells. Here, we characterize a region (amino acids 641-685) of HIV-1 gp41 that may be another site for gp41 binding. Besides peptides of the gp41 immunosuppressive domain, peptides of a second region (amino acids 641-685) could also inhibit rsgp41 (amino acids 539-684) binding to human cell lines U937 (monocytic cell line) and Raji (B cell line). An epitope (amino acids 669-674, ELDKWA) within this region is recognized by human monoclonal antibody 2F5. 2F5 shows broad-spectrum neutralizing capacity against HIV-1 laboratory strains and primary isolates (J. Virol. 1994, 68: 4031-4034; AIDS Res. Hum. Retrovir. 1994, 10: 1651-1658). We demonstrated by flow cytometry that mAb 2F5 could block gp41-binding to human cell lines H9 (T cells), Raji and U937, but the control mAb 4E10 that recognizes another region of gp41 (amino acids 686-728) and can not inhibit HIV infection, did not block this binding. These results indicate that the region (amino acids 641-685) of HIV-1 gp41 is the second site by which gp41 interacts with human cells, and suggest that the neutralization of HIV-1 infection by mAb 2F5 may be based on the fact that it blocks interaction of gp41 on virions with the gp41 binding molecules on human cells.
我们和其他研究人员之前的研究表明,HIV-1 gp41的免疫抑制结构域(氨基酸583 - 599)可与人T细胞、B细胞和单核细胞结合。在此,我们对HIV-1 gp41的一个区域(氨基酸641 - 685)进行了表征,该区域可能是gp41的另一个结合位点。除了gp41免疫抑制结构域的肽段外,第二个区域(氨基酸641 - 685)的肽段也能抑制重组gp41(氨基酸539 - 684)与人细胞系U937(单核细胞系)和Raji(B细胞系)的结合。该区域内的一个表位(氨基酸669 - 674,ELDKWA)可被人单克隆抗体2F5识别。2F5对HIV-1实验室毒株和原代分离株具有广谱中和能力(《病毒学杂志》1994年,68卷:4031 - 4034;《艾滋病研究与人类逆转录病毒》1994年,10卷:1651 - 1658)。我们通过流式细胞术证明,单克隆抗体2F5可阻断gp41与人细胞系H9(T细胞)、Raji和U937的结合,但识别gp41另一个区域(氨基酸686 - 728)且不能抑制HIV感染的对照单克隆抗体4E10则不能阻断这种结合。这些结果表明,HIV-1 gp41的该区域(氨基酸641 - 685)是gp41与人细胞相互作用的第二个位点,并提示单克隆抗体2F5对HIV-1感染的中和作用可能基于其阻断病毒体上的gp41与人类细胞上的gp41结合分子相互作用这一事实。