Brinchmann J E, Dobloug J H, Heger B H, Haaheim L L, Sannes M, Egeland T
Institute of Transplantation Immunology, National Hospital, Oslo, Norway.
J Infect Dis. 1994 Apr;169(4):730-8. doi: 10.1093/infdis/169.4.730.
To study the functional integrity of T cells from human immunodeficiency virus type 1 (HIV-1)-infected persons, CD4+ and CD8+ cells were examined for proliferation and secretion of interleukin-2 (IL-2) in response to staphylococcal superantigens and antibodies to CD3 and the alpha beta T cell receptor. A functional defect within CD8+ but not within CD4+ cells from HIV-1-infected persons was observed. Within CD8+ cells, proliferation and secretion of IL-2 was restricted to cells expressing the costimulatory molecule CD28. Such cells were proportionally reduced in HIV-1-infected persons. In patients with advanced immunodeficiency, however, evidence of functional derangement was found also within the CD28+ CD8+ cells. In a cross-sectional study of 73 HIV-infected persons and 15 controls, a significant correlation was observed between the number of CD28+ CD8+ cells and the presence of HIV-related disease. Our results suggest that regulation of expression of CD28 may play an important role in the immunopathogenesis of AIDS.
为研究来自人类免疫缺陷病毒1型(HIV-1)感染者的T细胞的功能完整性,检测了CD4⁺和CD8⁺细胞对葡萄球菌超抗原、抗CD3抗体及αβT细胞受体的增殖反应和白细胞介素-2(IL-2)分泌情况。观察到HIV-1感染者的CD8⁺细胞而非CD4⁺细胞存在功能缺陷。在CD8⁺细胞内,IL-2的增殖和分泌仅限于表达共刺激分子CD28的细胞。HIV-1感染者中此类细胞比例降低。然而,在晚期免疫缺陷患者中,在CD28⁺CD8⁺细胞内也发现了功能紊乱的证据。在一项对73名HIV感染者和15名对照者的横断面研究中,观察到CD28⁺CD8⁺细胞数量与HIV相关疾病的存在之间存在显著相关性。我们的结果表明,CD28表达的调节可能在艾滋病的免疫发病机制中起重要作用。