Aten J, Stet R J, Wagenaar-Hilbers J P, Weening J J, Fleuren G J, Nieuwenhuis P
Department of Pathology, University of Leiden, The Netherlands.
Scand J Immunol. 1992 Jan;35(1):93-105. doi: 10.1111/j.1365-3083.1992.tb02838.x.
Graft-versus-host reactions (GVHR) can be associated with several autoimmune phenomena involving the kidney as a target organ. By transferring lymphocytes of AO rats into complete Freund's adjuvant-pretreated (AO x BN)F1 hybrids, a dose-dependent GVHR with glomerulopathy was experimentally induced. IgM, IgG1, and IgG2a were deposited in the mesangial area and along the glomerular basement membrane. Eluted immunoglobulins from diseased kidneys bound to normal basement membranes and especially to laminin. Anti-laminin reactivity was also present in sera from F1 recipients with GVHR. Parental CD4+ T lymphocytes were required and sufficient to induce GVHR and glomerulopathy in sublethally irradiated F1 hybrids. Using various F1 hybrids, MHC class II incompatibility was shown to be required for the induction of GVHR-associated glomerulopathy. Across MHC class I incompatibility, GVHR without glomerulopathy could be induced, provided that both CD4+ and CD8+ donor T lymphocytes were administered. Finally, MHC incompatibility between donor T lymphocytes and the recipient non-lymphoid compartment was found to be sufficient for the induction of GVHR, but not for GVHR-associated glomerulopathy. The results indicate that alloreactive donor CD4+ T lymphocytes have to interact directly with MHC class II alloantigen bearing host B lymphocytes in order to stimulate the latter to produce (auto-)antibodies. GVHR-induced glomerulopathy shares several immunopathological features with HgCl2-induced autoimmune glomerulopathy in the rat.
移植物抗宿主反应(GVHR)可与多种以肾脏为靶器官的自身免疫现象相关。通过将AO大鼠的淋巴细胞转移至经完全弗氏佐剂预处理的(AO×BN)F1杂种动物体内,实验诱导出了伴有肾小球病的剂量依赖性GVHR。IgM、IgG1和IgG2a沉积于系膜区及沿肾小球基底膜分布。从患病肾脏洗脱的免疫球蛋白可与正常基底膜结合,尤其与层粘连蛋白结合。具有GVHR的F1受体血清中也存在抗层粘连蛋白反应性。亲代CD4+T淋巴细胞对于在亚致死剂量照射的F1杂种动物中诱导GVHR和肾小球病是必需且充分的。利用各种F1杂种动物,研究表明MHCⅡ类不相容性是诱导与GVHR相关的肾小球病所必需的。跨越MHCⅠ类不相容性,若同时给予CD4+和CD8+供体T淋巴细胞,则可诱导出无肾小球病的GVHR。最后,发现供体T淋巴细胞与受体非淋巴细胞区室之间的MHC不相容性足以诱导GVHR,但不足以诱导与GVHR相关的肾小球病。结果表明,同种反应性供体CD4+T淋巴细胞必须直接与携带MHCⅡ类同种抗原的宿主B淋巴细胞相互作用,以刺激后者产生(自身)抗体。GVHR诱导的肾小球病与大鼠中HgCl2诱导的自身免疫性肾小球病具有若干免疫病理学特征。