Santra S, Fultz P N, Letvin N L
Division of Viral Pathogenesis, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA.
J Virol. 1999 Aug;73(8):7065-9. doi: 10.1128/JVI.73.8.7065-7069.1999.
Chimpanzees have been important in studies of human immunodeficiency virus type 1 (HIV-1) pathogenesis and in evaluation of HIV-1 candidate vaccines. However, little information is available about HIV-1-specific cytotoxic T lymphocytes (CTL) in these animals. In the present study, in vitro stimulation of peripheral blood mononuclear cells (PBMC) from infected chimpanzees with HIV-1 Gag peptides was shown to be a sensitive, reproducible method of expanding HIV-1-specific CD8(+) effector CTL. Of interest, PBMC from two chimpanzees had CTL activity against Gag epitopes also recognized by major histocompatibility complex class I-restricted CTL from HIV-1-infected humans. The use of peptide stimulation will help to clarify the role of CTL in vaccine-mediated protection and HIV-1 disease progression in this important animal model.
黑猩猩在1型人类免疫缺陷病毒(HIV-1)发病机制研究以及HIV-1候选疫苗评估中具有重要作用。然而,关于这些动物体内HIV-1特异性细胞毒性T淋巴细胞(CTL)的信息却很少。在本研究中,用HIV-1 Gag肽体外刺激受感染黑猩猩的外周血单个核细胞(PBMC),被证明是一种扩增HIV-1特异性CD8(+)效应CTL的灵敏且可重复的方法。有趣的是,两只黑猩猩的PBMC对Gag表位具有CTL活性,这些表位也被HIV-1感染人类的主要组织相容性复合体I类限制性CTL所识别。肽刺激的应用将有助于阐明CTL在这一重要动物模型中疫苗介导的保护作用以及HIV-1疾病进展中的作用。