Guéry J C, Druet E, Glotz D, Hirsch F, Mandet C, De Heer E, Druet P
Unité 28, Institut National de la Santé et de la Recherche Médicale, Hôpital Broussais, Paris, France.
Eur J Immunol. 1990 Jan;20(1):93-100. doi: 10.1002/eji.1830200114.
Mercury-induced autoimmune glomerulonephritis in the Brown-Norway (BN) rat is characterized by the successive appearance of linear and granular glomerular IgG deposits. Anti-laminin autoantibodies represent the major part of the anti-glomerular basement membrane (GBM) antibodies produced in this model. Fusions were performed in this model and four anti-GBM monoclonal antibodies (mAb) were obtained. Three of them were laminin specific. Using rabbit anti-idiotype antibodies, cross-reactive idiotypes (CRId) were characterized on anti-laminin antibodies. They were expressed on the three anti-laminin mAb, on kidney-eluted and circulating anti-laminin antibodies. CRId-bearing immunoglobulins were detected transiently in the circulation and paralleled the anti-laminin antibody activity. By immunofluorescence studies on kidney cryostat sections two different CRId were defined. One was localized close to the antigen-combining site since it was not revealed on kidney-bound antibodies, in contrast with the second CRId. This latter CRId was also found deposited in a typical linear pattern in the early phase of the disease and in a granular pattern in the late phase, demonstrating that these CRId are components of immune deposits. Taken together, these results suggest that in this model of T-dependent polyclonal B cell activation, restricted sets of V genes encode for at least a part of the anti-GBM autoantibodies.
汞诱导的棕色挪威(BN)大鼠自身免疫性肾小球肾炎的特征是肾小球IgG沉积物呈线性和颗粒状相继出现。抗层粘连蛋白自身抗体是该模型中产生的抗肾小球基底膜(GBM)抗体的主要部分。在该模型中进行了融合,获得了四种抗GBM单克隆抗体(mAb)。其中三种是层粘连蛋白特异性的。使用兔抗独特型抗体,对抗层粘连蛋白抗体上的交叉反应独特型(CRId)进行了表征。它们在三种抗层粘连蛋白mAb、肾脏洗脱的和循环中的抗层粘连蛋白抗体上表达。携带CRId的免疫球蛋白在循环中短暂检测到,并与抗层粘连蛋白抗体活性平行。通过对肾脏冷冻切片的免疫荧光研究,确定了两种不同的CRId。一种位于靠近抗原结合位点的位置,因为与第二种CRId不同,它在肾脏结合抗体上未显示。后一种CRId在疾病早期也以典型的线性模式沉积,在晚期以颗粒模式沉积,表明这些CRId是免疫沉积物的组成部分。综上所述,这些结果表明,在这种T细胞依赖性多克隆B细胞激活模型中,有限的V基因集至少编码了部分抗GBM自身抗体。