vd Heuvel L P, Schröder C H, Savage C O, Menzel D, Assmann K J, Monnens L A, Veerkamp J H
Department of Biochemistry, University of Nijmegen, The Netherlands.
Pediatr Nephrol. 1989 Oct;3(4):406-13. doi: 10.1007/BF00850217.
Two children with Alport's syndrome are described, who developed anti-glomerular basement membrane (GMB) antibody-mediated nephritis after renal transplantation. The reactivity of antibodies in their serum with collagenase-solubilized normal GBM was examined by SDS-PAGE with one- and two-dimensional immunoblotting. The specificity was compared with that of antibodies present in serum from a patient with Goodpasture's syndrome, and a mouse monoclonal antibody (MCA-P1), directed against the Goodpasture antigen. All reacted in a similar way with collagenase-solubilized GBM. Since abnormalities in the composition of the GBM are present in Alport's syndrome, it is proposed that differing antigen composition of GBM in the host compared with the donor kidney, together with transplant rejection, may have provoked the development of post-transplant anti-GBM antibodies.
本文描述了两名患有阿尔波特综合征的儿童,他们在肾移植后发生了抗肾小球基底膜(GBM)抗体介导的肾炎。通过一维及二维免疫印迹的SDS-PAGE法检测了他们血清中抗体与胶原酶溶解的正常GBM的反应性。将其特异性与一名患有古德帕斯彻综合征患者血清中的抗体以及一种针对古德帕斯彻抗原的小鼠单克隆抗体(MCA-P1)进行了比较。所有这些抗体与胶原酶溶解的GBM反应方式相似。由于阿尔波特综合征存在GBM组成异常,因此有人提出,与供体肾相比,宿主GBM的抗原组成不同,再加上移植排斥反应,可能引发了移植后抗GBM抗体的产生。