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肠道固有层淋巴细胞对人类免疫缺陷病毒(HIV)感染细胞的细胞毒性活性。

Cytotoxic activity of intestinal lamina propria lymphocytes on human immunodeficiency virus (HIV)-infected cells.

作者信息

Di Massimo A M, Placido R, Bach S, Anastasi A M, Mastino A, Capobianchi M R, Colizzi V

机构信息

Department of Biology, II University of Rome, Italy.

出版信息

Immunology. 1992 May;76(1):117-21.

Abstract

The phenotype and cytotoxic activity of lamina propria lymphocytes (LPL) from the colorectal mucosa have been investigated primarily to analyse the role of LPL in human immunodeficiency virus (HIV) infection. The results reported here show that LPL strictly required a proliferative stimulus [either interleukin-2 (IL-2) or phytohaemaglutinin (PHA) to develop strong in vitro cytotoxicity, since freshly isolated LPL do not exhert cytotoxicity against either natural killer (NK)-sensitive or NK-resistant target cells. The cytotoxicity of activated LPL against a large panel of myeloid tumours or colorectal carcinoma target cells shows the irrelevance of the tissue origin of target cells. Moreover, activated LPL lysed HIV-infected H9 cells more efficiently than peripheral blood lymphocytes (PBL), and were susceptible to HIV infection. In contrast, unstimulated LPL failed to be cytotoxic and susceptible to HIV. Thus, we strongly suggest that for the lymphocytes of the colorectal mucosa expression of cytotoxic activity and susceptibility to HIV-infection show two faces of the same coin, and therefore may be relevant in understanding the mechanisms and paths of transmission of HIV infection.

摘要

对来自结直肠黏膜的固有层淋巴细胞(LPL)的表型和细胞毒性活性进行了研究,主要目的是分析LPL在人类免疫缺陷病毒(HIV)感染中的作用。此处报告的结果表明,LPL严格需要增殖刺激(白细胞介素-2(IL-2)或植物血凝素(PHA))才能在体外产生强大的细胞毒性,因为新鲜分离的LPL对自然杀伤(NK)敏感或NK抗性靶细胞均无细胞毒性。活化的LPL对大量髓系肿瘤或结直肠癌靶细胞的细胞毒性表明靶细胞的组织来源无关紧要。此外,活化的LPL比外周血淋巴细胞(PBL)更有效地裂解HIV感染的H9细胞,并且易受HIV感染。相比之下,未刺激的LPL没有细胞毒性且不易受HIV感染。因此,我们强烈建议,对于结直肠黏膜淋巴细胞而言,细胞毒性活性的表达和对HIV感染的易感性是同一枚硬币的两面,因此可能与理解HIV感染的机制和传播途径有关。

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