Villari D, Pollicino T, Spinella S, Russo F, Campo S, Rodino G, Squadrito G, Longo G, Raimondo G
Dipartimento di Patologia Umana, Università di Messina, Italy.
Am J Clin Pathol. 1995 Feb;103(2):136-40. doi: 10.1093/ajcp/103.2.136.
The aim of this study is to investigate whether hepatitis B e antigen (HBeAg) reactivity can be detected on formalin-fixed, paraffin-embedded liver tissue, and whether immunohistochemical detection of intrahepatic HBeAg may help to distinguish between "wild-type" and "eminus" hepatitis B virus (HBV) infection. Liver biopsy specimens were analyzed from 27 patients with chronic type B hepatitis: 12 patients had serum HBeAg (group A), and 15 patients were anti-HBe positive (group B). Part of each biopsy fragment was processed for histologic and immunohistochemical studies, and a part was used for HBV-DNA analysis. Dewaxed sections from each specimen were tested with a specific monoclonal anti-HBe antibody; then a Biotin-Streptavidin kit was used as detection system. HBeAg was revealed in 10 of 12 cases of group A and in 6 of the 15 cases of group B. Pre-core region of HBV genomes, isolated from each biopsy specimen, was analyzed by direct sequencing: 10 cases of group A were found to be infected by wild-type HBV alone and 2 cases by both wild and e-minus HBV types. In group B, all the 6 cases with intrahepatic HBeAg reactivity were found to be infected by mixed viral population, whereas the 9 cases negative for such reactivity were found to be infected by e-minus HBV alone. These results show that HBeAg can be detected in formalin-fixed, paraffin-embedded liver specimens, and the method is sensitive and specific. Because the presence of HBeAg in the liver indicates a wild-type HBV infection, and the lack of detection of such antigen in the hepatocytes of anti-HBe positive subjects correlates with unmixed e-minus HBV infection, the authors conclude that this technique is a useful tool for recognizing the viral strains that infect patients with chronic type B hepatitis.
本研究的目的是调查在福尔马林固定、石蜡包埋的肝组织上能否检测到乙肝e抗原(HBeAg)反应性,以及肝内HBeAg的免疫组化检测是否有助于区分“野生型”和“e-减型”乙型肝炎病毒(HBV)感染。对27例慢性乙型肝炎患者的肝活检标本进行了分析:12例患者血清HBeAg阳性(A组),15例患者抗-HBe阳性(B组)。每个活检片段的一部分用于组织学和免疫组化研究,另一部分用于HBV-DNA分析。用特异性单克隆抗-HBe抗体检测每个标本的脱蜡切片;然后使用生物素-链霉亲和素试剂盒作为检测系统。A组12例中的10例和B组15例中的6例检测到HBeAg。通过直接测序分析从每个活检标本中分离的HBV基因组前核心区:发现A组10例仅感染野生型HBV,2例同时感染野生型和e-减型HBV。在B组中,6例肝内有HBeAg反应性的患者均感染了混合病毒群体,而9例无此反应性的患者仅感染了e-减型HBV。这些结果表明,在福尔马林固定、石蜡包埋的肝标本中可以检测到HBeAg,且该方法灵敏且特异。由于肝内HBeAg的存在表明野生型HBV感染,而在抗-HBe阳性受试者的肝细胞中未检测到该抗原与单纯e-减型HBV感染相关,作者得出结论,该技术是识别感染慢性乙型肝炎患者的病毒株的有用工具。