Robert-Guroff M, Roilides E, Muldoon R, Venzon D, Husson R, Marshall D, Gallo R C, Pizzo P A
Laboratory of Tumor Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.
J Infect Dis. 1993 Mar;167(3):538-46. doi: 10.1093/infdis/167.3.538.
Protective immunity to human immunodeficiency virus (HIV) was examined in 228 serial sera from 58 HIV-infected children before and during antiretroviral therapy. Binding antibodies to putative protective V3 epitopes of HIV-1IIIB and HIV-1MN were investigated by a peptide ELISA, and neutralizing antibodies by inhibition of HIV-1MN cell-free viral infection. No difference in binding of total IgG or IgG subclasses was observed between patients with mild (group A) or advanced disease (group B). However, group A patients were more likely to possess neutralizing antibody titers > or = 225 (P = .040 after adjustment for CD4). This threshold titer also predicted clinical outcome in patients with age-adjusted CD4 count > 10% of normal median. Patients with titers < 225 more frequently encountered major clinical events during follow-up than did patients with titers > or = 225 (P = .0028). Epitopes other than the linear V3 loop contribute to this protective immune response. Identification of these epitopes should assist immune therapy of AIDS and HIV vaccine development.
在58名感染人类免疫缺陷病毒(HIV)的儿童接受抗逆转录病毒治疗之前及治疗期间,对其228份系列血清进行了HIV保护性免疫研究。通过肽酶联免疫吸附测定(ELISA)研究了针对HIV-1IIIB和HIV-1MN假定保护性V3表位的结合抗体,并通过抑制HIV-1MN无细胞病毒感染研究了中和抗体。在轻度疾病患者(A组)和晚期疾病患者(B组)之间,未观察到总IgG或IgG亚类结合的差异。然而,A组患者更有可能拥有中和抗体滴度≥225(校正CD4后P = 0.040)。该阈值滴度还可预测年龄校正CD4计数>正常中位数10%的患者的临床结局。随访期间,滴度<225的患者比滴度≥225的患者更频繁地发生重大临床事件(P = 0.0028)。除线性V3环外的其他表位也有助于这种保护性免疫反应。鉴定这些表位应有助于艾滋病的免疫治疗和HIV疫苗的开发。