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实验性及人类非甲非乙型肝炎的形态学与免疫组织化学

Morphology and immunohistochemistry of experimental and human non-A, non-B hepatitis.

作者信息

Schaff Z, Seto B, Coleman W G, Lapis K

机构信息

First Institute of Pathology and Experimental Cancer Research, Semmelweis Medical University, Budapest, Hungary.

出版信息

Tokai J Exp Clin Med. 1986;11 Suppl:111-20.

PMID:2454517
Abstract

The diagnosis of non-A, non-B hepatitis (NANBH) presently depends on the exclusion of hepatitis A, B and other causes of hepatitis, because no specific tests are available for diagnosis. Different approaches were used in order to detect NANBH infection in human and chimpanzee tissue. Endogenous interferon production was not detected in the weekly serum samples of 6 chimpanzees inoculated with a human agent of NANBH in contrast to the 5 HBV-infected animals. An antibody raised against a glycoprotein (GP77) associated with NANBH reacted immunohistochemically with liver biopsies obtained from NANBH-infected chimpanzees and with 11 out of 14 human liver biopsies from patients with NANBH. Two out of 12 human biopsies taken from patients with other liver diseases were positive. Diffuse reaction was noted in the cytoplasm of hepatocytes in chimpanzees. Three reaction patterns--diffuse, submembranous and perinuclear--were observed in human liver biopsies. A 35S radiolabeled DNA-probe of 780 base pairs--specific activity 5.4 x 10(4) cmp/micrograms DNA--isolated from NANBH-infected chimpanzees has been shown to hybridize in situ with liver sections from NANBH-infected chimpanzees. Data suggest that immunohistochemical and in situ hybridization methods can be successfully used for detection of NANBH infection in the liver of humans and chimpanzees.

摘要

目前,非甲非乙型肝炎(NANBH)的诊断依赖于排除甲型、乙型肝炎及其他肝炎病因,因为尚无特异性诊断检测方法。为检测人类和黑猩猩组织中的NANBH感染,采用了不同方法。与5只感染乙肝病毒的动物不同,在接种人类NANBH病原体的6只黑猩猩的每周血清样本中未检测到内源性干扰素产生。一种针对与NANBH相关的糖蛋白(GP77)产生的抗体,通过免疫组织化学方法与来自感染NANBH的黑猩猩的肝活检组织以及14例NANBH患者的11例人类肝活检组织发生反应。12例其他肝病患者的人类活检组织中有2例呈阳性。在黑猩猩肝细胞的细胞质中观察到弥漫性反应。在人类肝活检组织中观察到三种反应模式——弥漫性、膜下和核周。从感染NANBH的黑猩猩中分离出的一段780个碱基对的35S放射性标记DNA探针——比活性为5.4 x 10(4) cmp/微克DNA——已显示可与感染NANBH的黑猩猩的肝切片进行原位杂交。数据表明,免疫组织化学和原位杂交方法可成功用于检测人类和黑猩猩肝脏中的NANBH感染。

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