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多发性硬化症中细胞毒性T淋巴细胞反应的麻疹病毒-多肽特异性

Measles virus-polypeptide specificity of the cytotoxic T-lymphocyte response in multiple sclerosis.

作者信息

Dhib-Jalbut S, McFarlin D E, McFarland H F

机构信息

Neuroimmunology Branch, NINCDS, Bethesda, MD 20892.

出版信息

J Neuroimmunol. 1989 Feb;21(2-3):205-12. doi: 10.1016/0165-5728(89)90176-8.

Abstract

Some patients with multiple sclerosis (MS) have been shown previously to have a reduced capacity to generate measles virus (MV)-specific cytotoxic T-lymphocytes (CTLs). The mechanism of this reduction is not understood. Possibilities include sequestration of MV-CTLs within the central nervous system (CNS), abnormalities in regulation of this response (e.g., suppression), a defect in the T-cell repertoire of MS patients and a defect in the induction or maintenance of the CTL response to MV. To examine these possibilities, the CTL response to three purified polypeptides of MV (hemagglutinin (HA), fusion (F), and nucleocapsid (NC] was studied in eight healthy controls and 14 patients with multiple sclerosis. A defect in the response to two polypeptides of the virus (HA and NC) was found in the MS patients with reduced MV-CTL response. The response to F was also reduced but to a lesser extent. Limiting dilution analysis of the MV polypeptide-specific CTL response indicated that suppression is an unlikely cause for the reduction in CTL activity. The lymphoproliferative response to MV, HA, F, and NC was comparable in three MS patients and three controls examined. Together, the results of these studies indicate that the reduced MV-CTL response in MS patients was not due to a defect in the T-cell repertoire or sequestration due to cross-reactivity with a single myelin antigen. More likely mechanisms include abnormalities in the induction or maintenance of the MV-CTL response or sequestration within the CNS due to recognition of MV antigens.

摘要

先前已表明,一些多发性硬化症(MS)患者产生麻疹病毒(MV)特异性细胞毒性T淋巴细胞(CTL)的能力降低。这种降低的机制尚不清楚。可能的原因包括MV-CTL在中枢神经系统(CNS)内的隔离、这种反应调节异常(如抑制)、MS患者T细胞库缺陷以及对MV的CTL反应诱导或维持缺陷。为了研究这些可能性,在8名健康对照者和14名多发性硬化症患者中研究了对MV的三种纯化多肽(血凝素(HA)、融合蛋白(F)和核衣壳(NC))的CTL反应。在MV-CTL反应降低的MS患者中发现对病毒的两种多肽(HA和NC)反应存在缺陷。对F的反应也降低,但程度较轻。对MV多肽特异性CTL反应的有限稀释分析表明,抑制不太可能是CTL活性降低的原因。在检测的3名MS患者和3名对照者中,对MV、HA、F和NC的淋巴细胞增殖反应相当。总之,这些研究结果表明,MS患者中MV-CTL反应降低不是由于T细胞库缺陷或与单一髓鞘抗原交叉反应导致的隔离。更可能的机制包括MV-CTL反应诱导或维持异常或由于识别MV抗原而在CNS内隔离。

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