Rodriguez N, Yano N, Eylar E, Yamamura Y
Ponce School of Medicine AIDS Research Program, Puerto Rico 00732, USA.
Cell Mol Biol (Noisy-le-grand). 1997 Nov;43(7):951-8.
Qualitative and quantitative changes in immune functions of different T-cell subsets associated with infection by human immunodeficiency virus type 1 (HIV-1) were analyzed by flow cytometric assessment of intracytoplasmic cytokines. The T(H)1 cytokines, interleukin-2 (IL-2) and interferon-gamma (IFN-gamma), were produced by both CD4 and CD8 T-cell subsets. When normal peripheral blood mononuclear cells (PBMC) were activated in culture, both cytokines were produced predominantly by CD4 (CD4) cell and only a minor fraction of normal CD8 cells produced these cytokines. In the cultures of PBMC from HIV-1-infected individuals (HIV+PBMC), more HIV+CD8 cells produced IL-2 and IFN-gamma. Production of IFN-gamma by HIV+CD4 cells was markedly reduced, while IL-2nd tumor necrosis factor-alpha (TNF-alpha) production by HIV+CD4 remained relatively intact until the disease progressed further. Normal CD4 cells which were isolated by using a cell sorter, FACSCalibur was still able to produce IL-2 and TNF-alpha. But for full production of IFN-gamma, normal CD4 required some accessory cells, the identity of which could not yet be established.
通过对细胞内细胞因子进行流式细胞术评估,分析了与1型人类免疫缺陷病毒(HIV-1)感染相关的不同T细胞亚群免疫功能的定性和定量变化。辅助性T细胞1(TH1)细胞因子白细胞介素-2(IL-2)和干扰素-γ(IFN-γ)由CD4和CD8 T细胞亚群产生。当正常外周血单个核细胞(PBMC)在培养中被激活时,这两种细胞因子主要由CD4(CD4)细胞产生,只有一小部分正常CD8细胞产生这些细胞因子。在来自HIV-1感染个体的PBMC(HIV + PBMC)培养物中,更多的HIV + CD8细胞产生IL-2和IFN-γ。HIV + CD4细胞产生IFN-γ的能力明显降低,而HIV + CD4细胞产生IL-2和肿瘤坏死因子-α(TNF-α)的能力在疾病进一步进展之前仍相对保持完整。使用细胞分选仪FACSCalibur分离的正常CD4细胞仍能够产生IL-2和TNF-α。但对于IFN-γ的完全产生,正常CD4细胞需要一些辅助细胞,其身份尚未确定。