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多发性硬化症中T8 +细胞介导的抑制和细胞毒性功能比较

Comparison of T8+ cell-mediated suppressor and cytotoxic functions in multiple sclerosis.

作者信息

Antel J P, Nicholas M K, Bania M B, Reder A T, Arnason B G, Joseph L

出版信息

J Neuroimmunol. 1986 Sep;12(3):215-24. doi: 10.1016/s0165-5728(86)80005-4.

Abstract

Patients with progressive multiple sclerosis (MS) and controls were compared with regard to: (a) in vitro pokeweed mitogen (pwm)-induced IgG secretion, as an indirect measure of T8+ cell-mediated suppressor function; (b) alloantigen-directed cytotoxic activity, a predominantly T8+ cell-mediated function. The MS group had increased IgG secretion (4790 +/- 372 ng/ml vs. 1866 +/- 233 ng/ml, P less than 0.001) compared to controls. In contrast, alloantigen-directed cytotoxic activity did not differ between MS and control groups. These results suggest a selective defect of suppressor cell function in MS rather than a generalized dysfunction of T8+ cells. Defective immunoregulatory control coupled with preserved effector functions may contribute to the autoimmune process, suspected to underlie the pathogenesis of MS.

摘要

对进行性多发性硬化症(MS)患者和对照组在以下方面进行了比较:(a)体外商陆有丝分裂原(PWM)诱导的IgG分泌,作为T8 +细胞介导的抑制功能的间接指标;(b)同种异体抗原导向的细胞毒性活性,这是一种主要由T8 +细胞介导的功能。与对照组相比,MS组的IgG分泌增加(4790±372 ng/ml对1866±233 ng/ml,P<0.001)。相反,MS组和对照组之间的同种异体抗原导向的细胞毒性活性没有差异。这些结果表明MS中存在抑制细胞功能的选择性缺陷,而不是T8 +细胞的普遍功能障碍。免疫调节控制缺陷与效应功能保留相结合可能导致自身免疫过程,怀疑这是MS发病机制的基础。

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