Borrow P, Lewicki H, Hahn B H, Shaw G M, Oldstone M B
Department of Neuropharmacology, Scripps Research Institute, La Jolla, California 92037.
J Virol. 1994 Sep;68(9):6103-10. doi: 10.1128/JVI.68.9.6103-6110.1994.
Human immunodeficiency virus type 1 (HIV-1) Env-, Gag-, Pol-, Nef-, and Tat-specific cytotoxic T-lymphocyte (CTL) activities were quantitated temporally in five patients with symptomatic primary HIV-1 infection. A dominant CD8(+)-mediated, major histocompatibility complex class I-restricted CTL response to the HIV-1 envelope glycoprotein, gp160, was noted in four of the five patients studied. The level of HIV-1-specific CTL activity in the five patients paralleled the efficiency of control of primary viremia. Patients who mounted strong gp160-specific CTL responses showed rapid reduction of acute plasma viremia and antigenemia, while in contrast, primary viremia and antigenemia were poorly controlled in patients in whom virus-specific CTL activity was low or undetectable. These results suggest that HIV-1-specific CTL activity is a major component of the host immune response associated with the control of virus replication following primary HIV-1 infection and have important implications for the design of antiviral vaccines.
对五例有症状的原发性人类免疫缺陷病毒1型(HIV-1)感染患者,对其HIV-1包膜、群特异性抗原、多聚酶、负调控因子和反式激活因子特异性细胞毒性T淋巴细胞(CTL)活性进行了时间定量分析。在研究的五例患者中,有四例观察到由CD8(+)介导的、主要组织相容性复合体I类分子限制的针对HIV-1包膜糖蛋白gp160的CTL优势反应。五例患者中HIV-1特异性CTL活性水平与原发性病毒血症的控制效率平行。产生强烈gp160特异性CTL反应的患者急性血浆病毒血症和抗原血症迅速降低,相反,病毒特异性CTL活性低或检测不到的患者原发性病毒血症和抗原血症控制不佳。这些结果表明,HIV-1特异性CTL活性是宿主免疫反应的主要组成部分,与原发性HIV-1感染后病毒复制的控制相关,并且对抗病毒疫苗的设计具有重要意义。