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环孢菌素A对不同细胞密度的T淋巴细胞混合淋巴细胞培养诱导的增殖和细胞毒性反应的差异效应。

Differential effect of cyclosporin-A on the mixed-lymphocyte culture-induced proliferative and cytotoxic responses of T lymphocytes with different cell densities.

作者信息

Bejarano M T, Masucci M G, Klein E

出版信息

Cell Immunol. 1986 Dec;103(2):409-16. doi: 10.1016/0008-8749(86)90100-0.

Abstract

We have analyzed the effect of cyclosporin-A (CsA) on the proliferative and cytotoxic responses induced by mixed-lymphocyte cultures (MLC-s) on low and high density T lymphocytes. Allogeneic stimulation had a different impact on the two subsets. Proliferative and cytotoxic responses were inversely correlated; i.e., high density cells proliferated but exerted low levels of cytotoxicity while the lytic activity of the low density subset was stronger and the proliferation was weak. CsA impaired the proliferative and cytotoxic responses of the high density T lymphocytes but influenced less markedly the response of the low density cells. In both subsets CsA inhibited the MLC-induced interleukin 2 (IL-2) production. The generation of specific cytotoxicity was markedly suppressed by CsA, whereas the generation of anomalous activity was less affected. Addition of exogenous IL-2 to the CsA-containing cultures fully restored the proliferation and the generation of nonspecific cytotoxicity. In contrast, addition of interferon gamma (IFN-gamma) restored neither of these responses. However, for complete restoration of the stimulation-specific cytotoxicity, addition of both lymphokines was required. Taken together these results suggest that the CsA-induced suppression of the lymphokine production has different consequences in the low and high density subsets; the expression of anomalous and specific cytotoxicities require different signals; CsA interferes with several steps in the T-cell activation.

摘要

我们分析了环孢素A(CsA)对混合淋巴细胞培养(MLC)诱导的低密度和高密度T淋巴细胞增殖及细胞毒性反应的影响。同种异体刺激对这两个亚群有不同影响。增殖反应和细胞毒性反应呈负相关,即高密度细胞增殖但细胞毒性水平低,而低密度亚群的裂解活性更强但增殖较弱。CsA损害高密度T淋巴细胞的增殖和细胞毒性反应,但对低密度细胞反应的影响不太明显。在两个亚群中,CsA均抑制MLC诱导的白细胞介素2(IL-2)产生。CsA显著抑制特异性细胞毒性的产生,而异常活性的产生受影响较小。向含CsA的培养物中添加外源性IL-2可完全恢复增殖和非特异性细胞毒性的产生。相反,添加干扰素γ(IFN-γ)不能恢复这些反应中的任何一个。然而,为了完全恢复刺激特异性细胞毒性,需要同时添加两种淋巴因子。综合这些结果表明,CsA诱导的淋巴因子产生抑制在低密度和高密度亚群中有不同后果;异常和特异性细胞毒性的表达需要不同信号;CsA干扰T细胞活化的多个步骤。

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