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作 者:余永胜[1,2,3] 潘沛恩[1,2,3] 侯英勇[1,2,3] 张瑞云 张琴冈[1,2,3]
机构地区:[1]皖南医学院弋矶山医院,山东医科大学 [2]=,解放军第一四八医院 [3]济南市传染病院
出 处:《中华传染病杂志》1996年第3期134-136,共3页Chinese Journal of Infectious Diseases
摘 要:为观察细胞间粘附分子-1(ICAM-1)在乙型肝炎肝组织内的表达状况,探讨ICAM-1在乙型肝炎肝细胞免疫损伤中的作用。采用链菌素亲生物蛋白法(LSAB),以ICAM-1的单克隆抗体,检测104例急、慢性乙型肝炎,9例无症状携带者,10例正常肝组织标本内ICAM-1抗原表达情况。结果发现:ICAM-1在正常肝细胞无表达,肝窦内皮细胞弱表达;HBV感染后肝细胞呈不同程度的表达,肝窦内皮表达增强;中、重度慢性肝炎,活动性肝硬化肝细胞ICAM-1表达较急性肝炎,轻度慢性肝炎显著增强(P<0.01);急性肝炎较轻度慢性肝炎显著增强(P<0.01);轻度慢性肝炎较无症状携带者,正常肝组织显著增强(P<0.01)。表明ICAM-1在乙型肝炎肝细胞内表达与肝细胞损伤有关,对HBV的清除可能起着重要作用,ICAM-1在肝窦内皮的表达有助于淋巴细胞向肝组织内浸润。In order to study the role of intercellular adhesion molecule-1(ICAM-1)in the mechanism of hepatocellular immune injury,the expression status of ICAM-1 was observed in hep-atitis B.Labelling streptoavidin biotin (LSAB) was a sensitive method.By using monoclonal anti-body of ICAM-1,113 liver biopsy specimens including 104 cases of acute or chronic hepatitis B and 9 cases of HBV asymptomatic carrier were examined and l0 normal liver specimens were detected in the mean time. Hepatocytes had no ICAM-1 expression andsinusoidal endotheliocytes showed low level of ICAM-1 expression in normal liver tissues.In HBV infected cases,hepatocytes demonstrat-ed ICAM-1 expression to different degrees,while sinusoidal endotheliocyte expression increased.Enhanced expression of ICAMlon hepatocyte membrane or cytoplasm was observed in moderate or severe chronic hepatitis B and in active cirrhosis in comparision with acute hepatitis B and mild chronic hepatitis B (P< 0.01).Increased expression of ICAM-1 was observed in acute hepatitis in conparision with mild chronic hepatitis(P<0.01).And expression of ICAM-1 in chronic hepatitis also increased compared to asymptomatic carrier and normal liver(P<0.01).We concluded that the expression of ICAM-1 on hepatocytes was involved in the mechanism of hepatocellular immune in-jury and might play an important role in eliminating HBV.The ICAM-1 expression of sinusoidal en-dotheliocyte contributed to lymphocyte infiltrating toward liver tissue.
分 类 号:R512.620.2[医药卫生—内科学]
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