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肾移植排斥反应期间T淋巴细胞与肾上皮细胞之间的相互作用。

Interaction between T lymphocytes and kidney epithelial cells during renal allograft rejection.

作者信息

Kirby J A, Rajasekar M R, Lin Y, Proud G, Taylor R M

机构信息

Department of Surgery, Medical School, University of Newcastle upon Tyne, England, United Kingdom.

出版信息

Kidney Int Suppl. 1993 Jan;39:S124-8.

PMID:7682262
Abstract

Cultured human renal epithelial cells were treated with the cytokines IFN-gamma and TNF-alpha and alteration in expression and function of markers including Classes I and II MHC antigens and the adhesion molecules LFA-3 and ICAM-1 was examined. It was found that a mixture of IFN-gamma and TNF-alpha induced Class II MHC antigens, up-regulated expression of Class I, LFA-3 and ICAM-1 molecules and enhanced binding of 51Cr-labeled mononuclear immune cells. However, lymphocytes failed to proliferate in response to allo-stimulation by renal epithelial cells. Lymphocytes recovered after four days in mixed culture with allogeneic renal cells were purified and re-stimulated with irradiated spleen cells for five days prior to measurement of proliferation. These lymphocytes failed to proliferate if the spleen cells were syngeneic with the renal cells used in the primary stimulation. However, if the renal cells were from a third-party donor the lymphocytes showed a normal proliferative response to the allogeneic spleen cells. It has been demonstrated that cytokine-stimulated renal epithelial cells bind, but fail to initiate proliferation of, resting allogenic lymphocytes and that activated renal cells can specifically anergise potentially graft damaging allospecific T lymphocytes.

摘要

用细胞因子γ干扰素(IFN-γ)和肿瘤坏死因子-α(TNF-α)处理培养的人肾上皮细胞,并检测包括Ⅰ类和Ⅱ类主要组织相容性复合体(MHC)抗原以及黏附分子淋巴细胞功能相关抗原-3(LFA-3)和细胞间黏附分子-1(ICAM-1)在内的标志物的表达和功能变化。结果发现,IFN-γ和TNF-α的混合物可诱导Ⅱ类MHC抗原,上调Ⅰ类、LFA-3和ICAM-1分子的表达,并增强51Cr标记的单核免疫细胞的结合。然而,淋巴细胞对肾上皮细胞的同种异体刺激无增殖反应。将与同种异体肾细胞混合培养4天后恢复的淋巴细胞纯化,并用经照射的脾细胞再次刺激5天,然后检测增殖情况。如果脾细胞与初次刺激所用的肾细胞是同基因的,则这些淋巴细胞不会增殖。然而,如果肾细胞来自第三方供体,则淋巴细胞对同种异体脾细胞表现出正常的增殖反应。已证明细胞因子刺激的肾上皮细胞可结合静止的同种异体淋巴细胞,但不能启动其增殖,并且活化的肾细胞可特异性地使可能损害移植物的同种特异性T淋巴细胞失能。

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