Biewenga J, Noordhoek G T, Donker A J, Beukhof J R
Department of Histology, Medical Faculty, Free University, Amsterdam, The Netherlands.
Nephron. 1987;47(4):295-8. doi: 10.1159/000184527.
An IgA nephropathy model based on long-term oral administration of protein antigens was evaluated in three mouse strains using trinitrophenyl (TNP)-conjugated ovalbumin. Administration of the antigen for 14 weeks did not induce a significant IgA response nor deposition of IgA in the mesangium in any of the mouse strains. If, however, serum IgA anti-TNP antibodies were induced by intraperitoneal injection of anti-TNP producing MOPC-315 tumor cells, subsequent intravenous injection of antigen resulted in the deposition of IgA immune complexes in the mouse kidneys. Hematuria did not occur. In conclusion, previous data showing that long-term oral administration of protein antigens induces mesangial IgA deposits could not be confirmed with TNP ovalbumin. However, mesangial IgA deposits were obtained in animals treated with MOPC-315 tumor cells as described by Rifai et al. [J. exp. Med. 150: 1161-1173, 1979].
利用三硝基苯基(TNP)偶联的卵清蛋白,在三种小鼠品系中评估了基于长期口服蛋白质抗原的IgA肾病模型。给抗原14周在任何小鼠品系中均未诱导出显著的IgA反应,也未在系膜中诱导IgA沉积。然而,如果通过腹腔注射产生抗TNP的MOPC - 315肿瘤细胞诱导血清IgA抗TNP抗体,随后静脉注射抗原会导致IgA免疫复合物在小鼠肾脏中沉积。未出现血尿。总之,先前显示长期口服蛋白质抗原可诱导系膜IgA沉积的数据,用TNP卵清蛋白无法证实。然而,如Rifai等人[《实验医学杂志》150: 1161 - 1173, 1979]所述,在用MOPC - 315肿瘤细胞处理的动物中获得了系膜IgA沉积。