Hoyer J R, Seiler M W
Am J Kidney Dis. 1986 Jan;7(1):69-75. doi: 10.1016/s0272-6386(86)80058-0.
Kidneys were transplanted from rats with immune complex nephritis to normal rats to determine the role of circulating antibodies to renal antigens in the maintenance of immune complexes. Glomerular subepithelial immune complexes in nine proteinuric donor rats, actively or passively immunized with proximal tubular antigen Fx1A (active and passive Heymann nephritis), were studied at the time of transplantation and two to four and one-half months after transplantation to normal unilaterally nephrectomized recipient rats. These subepithelial IgG deposits and proteinuria persisted throughout the four-month period after transplantation. Tubular subepithelial immune complexes in the kidneys of nine rats, actively immunized with a distal renal tubular antigen, Tamm-Horsfall protein, were studied at the time of transplantation when donors had high circulating IgG antibody titers to Tamm-Horsfall protein and at one to eight weeks after transplantation. The abundant granular and nodular immune complexes of rat IgG and Tamm-Horsfall protein at the base of tubular cells were very rapidly cleared during the first two weeks after transplantation and were virtually absent by four weeks. The rapid clearance of tubular immune complexes after transplantation of kidneys from actively immunized rats followed a time course similar to that after passive immunization with antisera to Tamm-Horsfall protein. These findings support the concept that high titers of circulating antibodies to Tamm-Horsfall protein are required to prevent the rapid clearance of tubular immune complexes, a process that is facilitated by conditions of antigen excess at the surface of tubular cells.(ABSTRACT TRUNCATED AT 250 WORDS)
将患有免疫复合物性肾炎的大鼠的肾脏移植到正常大鼠体内,以确定循环抗肾抗原抗体在免疫复合物维持中的作用。对9只蛋白尿供体大鼠(主动或被动用近端肾小管抗原Fx1A免疫,即主动和被动海曼肾炎)的肾小球上皮下免疫复合物,在移植时以及移植到正常单侧肾切除受体大鼠后2至4个半月进行了研究。这些上皮下IgG沉积物和蛋白尿在移植后的四个月期间一直存在。对9只大鼠的肾脏中的肾小管上皮下免疫复合物进行了研究,这些大鼠主动用远端肾小管抗原Tamm-Horsfall蛋白免疫,在移植时供体对Tamm-Horsfall蛋白有高循环IgG抗体滴度,以及在移植后1至8周进行研究。在移植后的头两周内,肾小管细胞底部大量的大鼠IgG和Tamm-Horsfall蛋白的颗粒状和结节状免疫复合物被迅速清除,到四周时几乎消失。主动免疫大鼠肾脏移植后肾小管免疫复合物的快速清除过程与用抗Tamm-Horsfall蛋白抗血清被动免疫后的时间进程相似。这些发现支持了这样的概念,即需要高滴度的循环抗Tamm-Horsfall蛋白抗体来防止肾小管免疫复合物的快速清除,这一过程在肾小管细胞表面抗原过量的情况下会加速。(摘要截短至250字)