Neurath A R, Strick N, Taylor P, Rubinstein P, Stevens C E
Lindsley F. Kimball Research Institute, New York Blood Center, NY 10021.
AIDS Res Hum Retroviruses. 1990 Oct;6(10):1183-92. doi: 10.1089/aid.1990.6.1183.
It is essential for the development of strategies for prevention and therapy of human immunodeficiency virus (HIV-1) infections to define host factors playing a dominant role in determining the clinical outcome of infection. Antibodies directed against restricted regions of the HIV-1 glycoproteins gp120 and gp41 are likely to represent important factors involved in host defense against HIV-1. Definition of qualitative and quantitative differences in the spectrum of anti-gp120 and anti-gp41 antibodies between two vastly different groups of HIV-1-infected individuals, long-term asymptomatic carriers, and individuals with acquired immunodeficiency syndrome (AIDS) who died, might reveal the epitope specificity of antibodies contributing to prevention of clinical disease. To accomplish this goal, sera from both groups were assayed for antibodies recognizing synthetic peptides from gp120/gp41 which were shown in earlier experiments to mimic epitopes on the two HIV-1 glycoproteins. None of the sera recognized all of the distinct 27 peptides from gp120 and gp41. The spectrum of antibodies was distinct for each of the sera from both groups of HIV-1-infected individuals. Nevertheless, antibody responses distinguishing the two groups from each other were discerned. In particular, it was possible to predict the unfavorable outcome of disease by comparative measurements of levels of antibodies to a peptide (303-338), corresponding to the entire V3 hypervariable loop of gp120 and/or by providing evidence for declining levels of these antibodies during the course of infection. Antibodies recognizing additional peptides [(219-245), (280-306), (425-452), (658-682), (729-758), (808-845), and (845-862)] were significantly less prevalent in AIDS patients than in asymptomatic carriers. It appears possible that maintenance of high levels of the respective antibodies would contribute to preventing AIDS in HIV-1-infected individuals. Active immunization with antigens containing epitopes defined by the respective peptides and/or administration of the corresponding antibodies may be considered as a modality for therapy of HIV-1 infections.
确定在决定感染临床结果中起主导作用的宿主因素,对于制定人类免疫缺陷病毒(HIV-1)感染的预防和治疗策略至关重要。针对HIV-1糖蛋白gp120和gp41受限区域的抗体可能是宿主抵御HIV-1的重要因素。定义两组截然不同的HIV-1感染个体(长期无症状携带者和已死亡的获得性免疫缺陷综合征患者)之间抗gp120和抗gp41抗体谱的定性和定量差异,可能会揭示有助于预防临床疾病的抗体的表位特异性。为实现这一目标,检测了两组的血清中识别来自gp120/gp41的合成肽的抗体,这些合成肽在早期实验中显示可模拟两种HIV-1糖蛋白上的表位。没有一份血清能识别来自gp120和gp41的所有27种不同肽段。两组HIV-1感染个体的每份血清的抗体谱都不同。然而,还是识别出了区分这两组的抗体反应。特别是,通过比较针对对应于gp120整个V3高变环的肽段(303-338)的抗体水平,和/或通过提供感染过程中这些抗体水平下降的证据,可以预测疾病的不良结局。识别其他肽段[(219-245)、(280-306)、(425-452)、(658-682)、(729-758)、(808-845)和(845-862)]的抗体在艾滋病患者中的流行率明显低于无症状携带者。维持相应抗体的高水平似乎可能有助于预防HIV-1感染个体患艾滋病。用含有由相应肽段定义的表位的抗原进行主动免疫和/或给予相应抗体,可被视为治疗HIV-1感染的一种方式。