[扩张型心肌病和心肌炎患者的免疫学背景:临床和实验研究]。

Journal of cardiography. Supplement Pub Date : 1986-01-01
C Kishimoto, A Matsumori, N Tomioka, T Sakurai, C Kawai
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引用次数: 0

摘要

免疫遗传机制可能参与了特发性心肌病的发病机制。病毒性心肌炎被认为是扩张型心肌病的一个原因。本研究通过微滴细胞毒性试验检测了心肌病(DCM)和心肌炎(MC)患者的主要组织相容性复合体(人白细胞抗原:HLA),激光流式细胞术检测了淋巴细胞亚群,以及植物血凝素(PHA)和魔豆蛋白A (Con A)诱导的淋巴细胞成胚活性。我们还采用免疫荧光技术检测了近交系小鼠脑心肌炎(EMC)病毒心肌炎的发病率和组织病理学,以及接种EMC病毒的DBA/2小鼠外周血T淋巴细胞和b淋巴细胞的一系列变化。结果如下:主要组织相容性复合体(HLA和H-2);DCM患者HLA-B12和MC患者HLA-DR8的出现频率高于对照组。在EMC病毒感染中,近交系A/J (H-2a)、C57BL/6 (H-2b)、BALB/c (H-2d)、DBA/2 (H-2d)和C3H/He (H-2k)小鼠发生MC的频率存在差异。遗传机制可能起着类似于DCM患者病变的作用,在慢性mc2期DBA/2小鼠中发现了对病毒感染的易感性。淋巴细胞群研究;在DCM和肥厚性心肌病(HCM)患者中,okt8(抑制性t细胞)明显低于对照组。与对照组相比,MC患者淋巴细胞亚群无明显变化。(摘要删节250字)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Immunological background of patients with dilated cardiomyopathy and myocarditis: clinical and experimental studies].

Immunogenetic mechanism may be involved in the pathogenesis of idiopathic cardiomyopathy. Viral myocarditis is considered a cause of dilated cardiomyopathy. In this study, we examined the major histocompatibility complexes (human leukocyte antigens: HLA) by microdroplet cytotoxicity test, lymphocyte subsets by laser flow cytometry, and the activity of lymphocyte blastoformation induced by phytohemagglutinin (PHA) and concanavalin A (Con A) in patients with cardiomyopathies (DCM) and myocarditis (MC). We also examined the incidence and histopathology of encephalomyocarditis (EMC) virus myocarditis in inbred strains of mice, and serial changes of T- and B-lymphocytes in the peripheral blood of DBA/2 mice inoculated with EMC virus by immunofluorescence techniques. The results were as follows: Major histocompatibility complex (HLA and H-2); HLA-B12 in patients with DCM and HLA-DR8 in patients with MC were more frequent than in controls. In EMC virus infection, differences were found in the frequency of occurrence of MC in inbred strains of A/J (H-2a), C57BL/6 (H-2b), BALB/c (H-2d), DBA/2 (H-2d) and C3H/He (H-2k) mice. Genetic mechanism may play a role heart similar to lesions in patients with DCM were seen in DBA/2 mice in the chronic stage of MC. in susceptibility to virus infection. Lymphocyte population study; OKT 8 (suppressor T-cell) was significantly lower in patients with DCM and hypertrophic cardiomyopathy (HCM) than in controls. There were no significant changes of lymphocyte subsets in patients with MC as compared with the controls.(ABSTRACT TRUNCATED AT 250 WORDS)

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