Meyer zum Büschenfelde K H, Manns M, Hütteroth T H, Hopf U, Arnold W
Clin Exp Immunol. 1979 Aug;37(2):205-12.
Two different types of immune reactions against liver membrane antigens have been described: firstly, cell-mediated immunity and autoantibodies against the liver-specific protein (LSP) in HBsAg-negative and HBsAg-positive chronic active hepatitis (CAH), and secondly, a liver membrane autoantibody (LMA) in HBsAg-negative CAH. Using 100,000 g supernatants of human and rabbit liver homogenates, the corresponding antigen of LMA could be separated by affinity chromatography on insolubilized LMA-positive sera from patients with HBsAg-negative CAH. A further characterization by crossed immunoelectrophoresis showed that LMA is directed against a soluble liver membrane antigen (LM-Ag) that is not a constituent of the purified LSP. LM-Ag seems to be species-unspecific and moves faster than LSP and serum albumin in crossed immunoelectrophoresis. While LSP is believed to be involved in the pathogenesis of HBsAg-negative and HBsAg-positive chronic active hepatitis, LM-Ag may be a target antigen only in cases of HBsAg-negative autoimmune CAH.
第一,在乙肝表面抗原(HBsAg)阴性和阳性的慢性活动性肝炎(CAH)中,针对肝脏特异性蛋白(LSP)的细胞介导免疫和自身抗体;第二,在HBsAg阴性的CAH中存在的肝细胞膜自身抗体(LMA)。使用人和兔肝脏匀浆的100,000g上清液,LMA的相应抗原可通过用HBsAg阴性CAH患者的LMA阳性血清在不溶性介质上进行亲和层析来分离。通过交叉免疫电泳进一步表征表明,LMA针对的是一种可溶性肝细胞膜抗原(LM-Ag),它不是纯化LSP的组成部分。LM-Ag似乎是非种属特异性的,并且在交叉免疫电泳中比LSP和血清白蛋白移动得更快。虽然LSP被认为与HBsAg阴性和阳性慢性活动性肝炎的发病机制有关,但LM-Ag可能仅在HBsAg阴性自身免疫性CAH病例中是靶抗原。