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从感染HIV者的大肠活检组织中分离出的T细胞亚群分布、激活及分化异常。柏林腹泻/消瘦综合征研究小组。

Abnormalities in subset distribution, activation, and differentiation of T cells isolated from large intestine biopsies in HIV infection. The Berlin Diarrhoea/Wasting Syndrome Study Group.

作者信息

Schneider T, Ullrich R, Bergs C, Schmidt W, Riecken E O, Zeitz M

机构信息

Department of Medicine, Klinikum Steglitz, Free University of Berlin, Germany.

出版信息

Clin Exp Immunol. 1994 Mar;95(3):430-5. doi: 10.1111/j.1365-2249.1994.tb07014.x.

Abstract

Intestinal T cells have a unique state of activation and differentiation which might specifically affect or be affected by HIV infection. Lymphocyte subsets in the peripheral blood are well characterized, but our knowledge about intestinal lymphocytes in HIV infection is incomplete. We therefore analysed lymphocytes isolated from large intestine biopsies of AIDS patients and controls by three-colour cytofluorometry. In the large intestine of HIV-infected patients CD4 T cells were reduced and CD8 T cells were increased compared with controls. Most of the CD8 T cells in the colorectal mucosa of AIDS patients were of the cytotoxic phenotype. Activated and resting CD4 T cells were similarly reduced, the expression of CD25 and HLA-DR of CD8 T cells was unaltered and increased, respectively. In intestinal CD4 T cells the expression of CD29 was decreased, but the expression of CD45RO and HML-1 was normal. CD8 T cells had a decreased expression of all these differentiation markers. Our findings demonstrate substantial alterations in subset distribution, activation, and differentiation of large intestine T cells, which may contribute to the secondary infections and malignancies commonly observed in the gut of AIDS patients.

摘要

肠道T细胞具有独特的激活和分化状态,这可能会特异性地影响HIV感染或受其影响。外周血中的淋巴细胞亚群已得到充分表征,但我们对HIV感染时肠道淋巴细胞的了解并不完整。因此,我们通过三色细胞荧光分析法分析了从艾滋病患者和对照组的大肠活检组织中分离出的淋巴细胞。与对照组相比,HIV感染患者的大肠中CD4 T细胞减少,CD8 T细胞增加。艾滋病患者结直肠黏膜中的大多数CD8 T细胞具有细胞毒性表型。活化的和静息的CD4 T细胞同样减少,CD8 T细胞的CD25和HLA-DR表达分别未改变和增加。在肠道CD4 T细胞中,CD29的表达降低,但CD45RO和HML-1的表达正常。CD8 T细胞所有这些分化标志物的表达均降低。我们的研究结果表明,大肠T细胞的亚群分布、激活和分化存在显著改变,这可能导致艾滋病患者肠道中常见的继发感染和恶性肿瘤。

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