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白细胞介素与免疫抑制因子:一种调节系统?

Interleukins and immunosuppressive factors: a regulatory system?

作者信息

Blazsek I, Mathé G

出版信息

Biomed Pharmacother. 1983;37(6):258-65.

PMID:6322876
Abstract

On exogenous stimulus immunocompetent leucocytes produce antigen-specific factors, which essentially determine the magnitude and duration of T-lymphocyte dependent immunoreactions. Interleukin 1 (IL-1, monokin) and interleukin 2 (IL-2, lymphokine) form a bimodal amplification system which may operate in vivo at the level of peripheral lymphoid organs, which interleukin 3 (IL 3, lymphokine) may function as a positive feed-back signal at the level of multipotential stem cells. The physiological IL-2 has wider importance, since the permanent expression of Il-2 gene due to the insertion of the viral promoter sequence (HTLV in human) led to uncontrolled proliferation of T-cells and to the development of lymphomas and leukemias of mature T-cell phenotype. On the afferent arc of immunoreactions endogenous factors mediate T-cell proliferation inhibitory effect probably via interaction with the interleukin system. Some practical aspects of these two antagonistic group of factors are presented and discussed.

摘要

在外部刺激下,免疫活性白细胞产生抗原特异性因子,这些因子本质上决定了T淋巴细胞依赖性免疫反应的强度和持续时间。白细胞介素1(IL-1,单核因子)和白细胞介素2(IL-2,淋巴因子)形成一个双峰放大系统,该系统可能在外周淋巴器官水平在体内发挥作用,而白细胞介素3(IL-3,淋巴因子)可能在多能干细胞水平作为正反馈信号发挥作用。生理性IL-2具有更广泛的重要性,因为由于病毒启动子序列(人类中的HTLV)的插入导致Il-2基因的持续表达,从而导致T细胞不受控制的增殖以及成熟T细胞表型的淋巴瘤和白血病的发生。在免疫反应的传入弧上,内源性因子可能通过与白细胞介素系统相互作用介导T细胞增殖抑制作用。本文介绍并讨论了这两类拮抗因子的一些实际方面。

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