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[从多发性硬化症患者获取的外周血淋巴细胞的干扰素产生及自然杀伤活性]

[Interferon production and natural killer activity of peripheral blood lymphocytes obtained from patients with multiple sclerosis].

作者信息

Maruo Y

机构信息

Department of Microbiology, Hokkaido University School of Medicine, Sapporo, Japan.

出版信息

Hokkaido Igaku Zasshi. 1988 Jul;63(4):521-33.

PMID:2464533
Abstract

Interferon (IFN) -system of patients with multiple sclerosis (MS) during the stable stage of the disease activity was investigated. Thirty six patients were divided into 3 groups of mild, moderate and severe patients according to the scores of disability status scale (DSS). IFN-alpha producibility and natural killer (NK) activity of peripheral blood lymphocytes (PBL) or large granular lymphocytes (LGL) fractionated from PBL were determined by culturing with HeLa cells persistently infected with measles virus (HeLa/MV) and K562 cells. IFN-gamma was induced in PBL obtained from the patients using killed cells of Propionibacterium acnes (P. acnes), Listeria monocytogenes (LM) and Streptococcus salivarius (Str. sal.) and a lectin of concanavalin A (Con A). Both IFN-alpha producibility and NK activity of PBL obtained from the patients were depressed in parallel with the severity of DSS of the patients. The depressed NK activity of the patients could be recovered by neither IFN-alpha nor interleukin-2 added exogenously. In addition, the induction of IFN-gamma was also depressed in the patients in response to P. acnes and LM, but not Str. sal. or Con A. These results suggest that the defect of IFN-system observed in PBL of the patients may result from the depressed function of both LGL and T lymphocyte subpopulations which are responsive to P. acnes and LM. It is postulated that these immunocompetent cells might migrate to subclinical demyelinating lesions of central nervous system where cytokines including IFN-gamma were produced locally, and that their migration might result in the quantitative decrease of lymphocytes participating in IFN-system in PBL of patients with MS.

摘要

对处于疾病活动稳定期的多发性硬化症(MS)患者的干扰素(IFN)系统进行了研究。根据残疾状态量表(DSS)评分,将36例患者分为轻度、中度和重度三组。通过与持续感染麻疹病毒的HeLa细胞(HeLa/MV)和K562细胞共培养,测定外周血淋巴细胞(PBL)或从PBL中分选的大颗粒淋巴细胞(LGL)的IFN-α产生能力和自然杀伤(NK)活性。使用痤疮丙酸杆菌(P. acnes)、单核细胞增生李斯特菌(LM)、唾液链球菌(Str. sal.)的灭活细胞和伴刀豆球蛋白A(Con A)凝集素诱导患者PBL产生IFN-γ。患者PBL的IFN-α产生能力和NK活性均与患者DSS的严重程度呈平行下降。患者NK活性的降低不能通过外源性添加IFN-α或白细胞介素-2来恢复。此外,患者对P. acnes和LM刺激的IFN-γ诱导也降低,但对Str. sal.或Con A刺激的诱导未降低。这些结果表明,在患者PBL中观察到的IFN系统缺陷可能是由于对P. acnes和LM有反应的LGL和T淋巴细胞亚群功能降低所致。据推测,这些免疫活性细胞可能迁移至中枢神经系统的亚临床脱髓鞘病变部位,在那里局部产生包括IFN-γ在内的细胞因子,并且它们的迁移可能导致MS患者PBL中参与IFN系统的淋巴细胞数量减少。

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