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膜攻击复合物和乙肝e抗原在膜性肾病中的免疫电子显微镜定位

Immunoelectron microscopic localization of membrane attack complex and hepatitis B e antigen in membranous nephropathy.

作者信息

Akano N, Yoshioka K, Aya N, Miyamoto H, Takemura T, Tohda M, Maki S

机构信息

Department of Pediatrics, Kinki University School of Medicine, Osaka-sayama, Japan.

出版信息

Virchows Arch A Pathol Anat Histopathol. 1989;414(4):325-30. doi: 10.1007/BF00734087.

Abstract

Immunoelectron microscopy was used to localize membrane attack complex (MAC) and hepatitis B e (HBe) antigen in renal tissue specimens from a total of 9 patients with membranous nephropathy (MN); 6 with MN associated with a hepatitis B virus (HBV) infection, 2 with idiopathic MN, and 1 with lupus nephritis. All the patients were proteinuric, and 2 patients were classified as stage I-II, 6 as stage II, and 1 as stage IV. MAC, along with IgG and C3, was distributed within the subepithelial electron dense deposits in all the stages. MAC was also stained in the striated membranous structures within the glomerular basement membrane and mesangial matrix of some patients. In HBV-associated MN, HBe antigen was localized in the subepithelial electron dense deposits of 5 patients, while it was absent from the subepithelial deposits in a patient that was sero-positive for hepatitis B s antigen but negative for HBe antigen. This patient also lacked MAC deposition in these loci. These results suggest that MAC is associated with the formation of subepithelial deposits and proteinuria in MN. In HBV-associated MN, HBe antigen-antibody immune complex makes up the subepithelial deposits and is likely to activate the terminal components of complement in situ.

摘要

免疫电子显微镜技术用于在总共9例膜性肾病(MN)患者的肾组织标本中定位膜攻击复合物(MAC)和乙肝e(HBe)抗原;其中6例MN与乙型肝炎病毒(HBV)感染相关,2例为特发性MN,1例为狼疮性肾炎。所有患者均有蛋白尿,2例患者分类为Ⅰ - Ⅱ期,6例为Ⅱ期,1例为Ⅳ期。在所有阶段,MAC与IgG和C3一起分布于上皮下电子致密沉积物内。在一些患者的肾小球基底膜和系膜基质的条纹状膜性结构中也检测到MAC染色。在HBV相关的MN中,5例患者的HBe抗原定位于上皮下电子致密沉积物,而1例乙肝表面抗原血清学阳性但HBe抗原阴性的患者上皮下沉积物中未检测到HBe抗原。该患者这些部位也缺乏MAC沉积。这些结果表明,MAC与MN中上皮下沉积物的形成及蛋白尿有关。在HBV相关的MN中,HBe抗原 - 抗体免疫复合物构成上皮下沉积物并可能原位激活补体终末成分。

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