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慢性活动性肝病中的细胞免疫和体液免疫反应。I. 未经治疗的特发性自身免疫性肝炎、慢性乙型活动性肝炎和原发性胆汁性肝硬化患者肝活检中的淋巴细胞亚群。

Cellular and humoral immune reactions in chronic active liver disease. I. Lymphocyte subsets in liver biopsies of patients with untreated idiopathic autoimmune hepatitis, chronic active hepatitis B and primary biliary cirrhosis.

作者信息

Eggink H F, Houthoff H J, Huitema S, Gips C H, Poppema S

出版信息

Clin Exp Immunol. 1982 Oct;50(1):17-24.

PMID:6983407
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1536867/
Abstract

In liver biopsies of 37 patients with chronic active liver disease (CALD) the inflammatory infiltrate was studied with monoclonal antibodies to the surface antigens on helper/inducer (OKT4+), suppressor/cytotoxic (OKT8+), killer/natural killer (OKM1,2+) cells and common T cell antigens (OKT1+, OKT3+). Furthermore OKT11 antibody was applied, which defines the E rosette receptor. Special emphasis was given to areas with piece-meal necrosis (PMN). In areas with PMN in idiopathic autoimmune CALD (IA-CALD, n = 15) OKT8+ and OKM+ lymphocytes and IgG plasma cells were present, whereas in hepatitis B-CALD (HB-CALD, n = 12) almost exclusively OKT8+ cells were found. In PBC (n = 10) OKT4+ cells in central parts of portal tracts and OKT8+ cells in areas with PMN predominated. These findings indicate that in IA-CALD antibody-dependent cell-mediated cytotoxicity (ADCC), as well as T cell cytotoxicity may be responsible for liver cell damage, while in HB-CALD T cell cytotoxicity seems to be the only mechanism. In PBC liver cell damage also predominantly is the result of T cell cytotoxicity. In addition, helper T lymphocytes seem to play a role since these are found in central areas of the portal tracts.

摘要

在37例慢性活动性肝病(CALD)患者的肝活检中,运用针对辅助/诱导性(OKT4+)、抑制/细胞毒性(OKT8+)、杀伤/自然杀伤(OKM1,2+)细胞以及常见T细胞抗原(OKT1+、OKT3+)表面抗原的单克隆抗体对炎性浸润进行了研究。此外,还应用了OKT11抗体,其可界定E玫瑰花结受体。研究特别关注了桥接坏死(PMN)区域。在特发性自身免疫性CALD(IA-CALD,n = 15)的PMN区域,存在OKT8+和OKM+淋巴细胞以及IgG浆细胞,而在乙型肝炎相关性CALD(HB-CALD,n = 12)中,几乎仅发现OKT8+细胞。在原发性胆汁性肝硬化(PBC,n = 10)中,门管区中央部分的OKT4+细胞以及PMN区域的OKT8+细胞占主导。这些发现表明,在IA-CALD中,抗体依赖性细胞介导的细胞毒性(ADCC)以及T细胞细胞毒性可能是肝细胞损伤的原因,而在HB-CALD中,T细胞细胞毒性似乎是唯一的机制。在PBC中,肝细胞损伤主要也是T细胞细胞毒性的结果。此外,辅助性T淋巴细胞似乎发挥了作用,因为在门管区中央区域发现了这些细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af6/1536867/b2759247d5cf/clinexpimmunol00163-0028-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af6/1536867/b2759247d5cf/clinexpimmunol00163-0028-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1af6/1536867/b2759247d5cf/clinexpimmunol00163-0028-a.jpg

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