Chehimi J, Bandyopadhyay S, Prakash K, Perussia B, Hassan N F, Kawashima H, Campbell D, Kornbluth J, Starr S E
Division of Infectious Diseases and Immunology, Joseph Stokes, Jr. Research Institute, Chiildren's Hospital of Philadelphia, Pennsylvania.
J Virol. 1991 Apr;65(4):1812-22. doi: 10.1128/JVI.65.4.1812-1822.1991.
Natural killer (NK) cells are a discrete subset of leukocytes, distinct from T and B lymphocytes. NK cells mediate spontaneous non-MHC-restricted killing of a wide variety of target cells without prior sensitization and appear to be involved in initial protection against certain viral infections. Depressed NK cell-mediated cytotoxicity, one of the many immunological defects observed in AIDS patients, may contribute to secondary virus infections. Here we report that clonal and purified polyclonal populations of NK cells, which expressed neither surface CD4 nor CD4 mRNA, were susceptible to infection with various isolates of human immunodeficiency virus type 1 (HIV-1). Viral replication was demonstrated by detection of p24 antigen intracellularly and in culture supernatants, by the presence of HIV DNA within infected cells, and by the ability of supernatants derived from HIV-infected NK cells to infect peripheral blood mononuclear cells or CD4+ cell lines. Infection of NK cells was not blocked by anti-CD4 or anti-Fc gamma RIII monoclonal antibodies. NK cells from HIV-infected and uninfected cultures were similar in their ability to lyse three different target cells. Considerable numbers of cells died in HIV-infected NK cell cultures. These results suggest that loss of NK cells in AIDS patients is a direct effect of HIV infection but that reduced NK cell function involves another mechanism. The possibility that NK cells serve as a potential reservoir for HIV-1 must be considered.
自然杀伤(NK)细胞是白细胞中的一个独特亚群,与T淋巴细胞和B淋巴细胞不同。NK细胞可介导对多种靶细胞的自发的非主要组织相容性复合体(MHC)限制的杀伤,无需预先致敏,并且似乎参与针对某些病毒感染的初始保护。NK细胞介导的细胞毒性降低是艾滋病患者中观察到的众多免疫缺陷之一,可能导致继发病毒感染。在此我们报告,既不表达表面CD4也不表达CD4 mRNA的NK细胞克隆和纯化的多克隆群体,易受1型人类免疫缺陷病毒(HIV-1)各种分离株的感染。通过在细胞内和培养上清液中检测p24抗原、通过感染细胞内存在HIV DNA以及通过来自HIV感染的NK细胞的上清液感染外周血单个核细胞或CD4 +细胞系的能力来证明病毒复制。抗CD4或抗FcγRIII单克隆抗体不能阻断NK细胞的感染。来自HIV感染和未感染培养物的NK细胞在裂解三种不同靶细胞的能力方面相似。在HIV感染的NK细胞培养物中有相当数量的细胞死亡。这些结果表明,艾滋病患者中NK细胞的丧失是HIV感染的直接后果,但NK细胞功能降低涉及另一种机制。必须考虑NK细胞作为HIV-1潜在储存库的可能性。