Simon M, Vincent C, Haftek M, Girbal E, Sebbag M, Gomès-Daudrix V, Serre G
Department of Biology and Pathology of the Cell, Toulouse-Purpan School of Medicine, University of Toulouse III, France.
Clin Exp Immunol. 1995 Apr;100(1):90-8. doi: 10.1111/j.1365-2249.1995.tb03608.x.
Since they were first described, serum IgG antibodies to the stratum corneum of rat oesophagus epithelium, highly specific for rheumatoid arthritis (RA), have been consensually called antikeratin antibodies (AKA). However, we recently demonstrated that they actually recognize three new proteins of rat oesophagus epithelium distinct from cytokeratins, and also human epidermal filaggrin. In this work we provided further evidence that AKA and RA-associated anti-filaggrin autoantibodies are the same antibodies. Moreover, analysing by indirect immunofluorescence on human skin a large series of 212 well characterized RA sera and anti-filaggrin autoantibodies purified from RA sera by affinity chromatography, we demonstrated the specific binding of AKA to the stratum corneum of human epidermis and the absence of any staining of the granular keratinocytes. This binding was confirmed and the AKA antigen precisely localized in human epidermis by immunoelectron microscopy. The antigen was found to be restricted to the filaggrin-containing intracellular fibrous matrix of the corneocytes, up to the desquamating cells. In contrast, MoAbs directed to human filaggrin and to profilaggrin, its precursor, not only stained the intracellular matrix of the lower corneocytes but also the keratohyalin granules of the granular cells, where profilaggrin is stored. These results reinforced by the absence of immunoblotting reactivity of RA sera to profilaggrin suggest that the epitopes recognized by AKA are absent from profilaggrin. Their identification may provide more insight into the pathogenesis of RA.
自从首次被描述以来,针对大鼠食管上皮角质层的血清IgG抗体,对类风湿关节炎(RA)具有高度特异性,一直被一致称为抗角蛋白抗体(AKA)。然而,我们最近证明,它们实际上识别大鼠食管上皮中三种不同于细胞角蛋白的新蛋白质,以及人类表皮丝聚合蛋白。在这项工作中,我们提供了进一步的证据,表明AKA和RA相关的抗丝聚合蛋白自身抗体是相同的抗体。此外,通过对人皮肤进行间接免疫荧光分析,我们检测了212份特征明确的RA血清,并对通过亲和层析从RA血清中纯化的抗丝聚合蛋白自身抗体进行了分析,结果表明AKA与人表皮角质层具有特异性结合,而颗粒状角质形成细胞没有任何染色。通过免疫电子显微镜证实了这种结合,并精确地定位了人表皮中的AKA抗原。发现该抗原局限于角质形成细胞中含丝聚合蛋白的细胞内纤维基质,直至脱落细胞。相比之下,针对人类丝聚合蛋白及其前体前丝聚合蛋白的单克隆抗体,不仅能染色下层角质形成细胞的细胞内基质,还能染色颗粒细胞中储存前丝聚合蛋白的透明角质颗粒。RA血清对前丝聚合蛋白缺乏免疫印迹反应性,这进一步证明了上述结果,表明前丝聚合蛋白不存在AKA识别的表位。对这些表位的鉴定可能会为RA的发病机制提供更多的见解。