Klein M R, van Baalen C A, Holwerda A M, Kerkhof Garde S R, Bende R J, Keet I P, Eeftinck-Schattenkerk J K, Osterhaus A D, Schuitemaker H, Miedema F
Department of Clinical Viro-Immunology, Central Laboratory of The Netherlands Red Cross Blood Transfusion Service, Amsterdam.
J Exp Med. 1995 Apr 1;181(4):1365-72. doi: 10.1084/jem.181.4.1365.
To gain more insight into the role of HIV-1-specific cytotoxic T lymphocytes (CTL) in the pathogenesis of AIDS, we investigated temporal relations between HIV-1 Gag-specific precursor CTL (CTLp), HIV-1 viral load, CD4+ T cell counts, and T cell function. Six HIV-1-infected subjects, who were asymptomatic for more than 8 yr with CD4+ counts > 500 cells/mm3, were compared with six subjects who progressed to AIDS within 5 yr after HIV-1 seroconversion. In the long-term asymptomatics, persistent HIV-1 Gag-specific CTL responses and very low numbers of HIV-1-infected CD4+ T cells coincided with normal and stable CD4+ counts and preserved CD3 mAb-induced T cell reactivity for more than 8 yr. In five out of six rapid progressors Gag-specific CTLp were also detected. However, early in infection the number of circulating HIV-1-infected CD4+ T cells increased despite strong and mounting Gag-specific CTL responses. During subsequent clinical progression to AIDS, loss of Gag-specific CTLp coincided with precipitating CD4+ counts and severe deterioration of T cell function. The possible relationships of HIV-1 Gag-specific CTLp to disease progression are discussed.
为了更深入了解HIV-1特异性细胞毒性T淋巴细胞(CTL)在艾滋病发病机制中的作用,我们研究了HIV-1 Gag特异性前体细胞毒性T淋巴细胞(CTLp)、HIV-1病毒载量、CD4+ T细胞计数和T细胞功能之间的时间关系。将6名感染HIV-1且无症状超过8年、CD4+细胞计数>500个/mm3的受试者与6名在HIV-1血清转化后5年内进展为艾滋病的受试者进行了比较。在长期无症状感染者中,持续的HIV-1 Gag特异性CTL反应和极少量的HIV-1感染CD4+ T细胞与正常且稳定的CD4+细胞计数以及超过8年的CD3单克隆抗体诱导的T细胞反应性保留同时存在。在6名快速进展者中的5名中也检测到了Gag特异性CTLp。然而,在感染早期,尽管有强烈且不断增强的Gag特异性CTL反应,循环中HIV-1感染的CD4+ T细胞数量仍增加。在随后临床进展为艾滋病的过程中,Gag特异性CTLp的丧失与CD4+细胞计数的急剧下降和T细胞功能的严重恶化同时发生。讨论了HIV-1 Gag特异性CTLp与疾病进展的可能关系。