Department of Pathology, Tokyo Women's Medical University, Tokyo, Japan.
Clin Transplant. 2011 Mar-Apr;25(2):191-200. doi: 10.1111/j.1399-0012.2010.01213.x.
The etiology of de novo membranous nephropathy (MN) after kidney transplantation is still uncertain. Immunological response to various allograft antigens is speculated to be a candidate for the etiology.
Seventeen patients with post-transplant de novo MN were studied clinically and pathologically in comparison with control post-transplant patients without MN. Double immunofluorescent staining was performed to identify the presence of donor-specific human leukocyte antigen (HLA) combined with IgG in the deposits on glomerular capillary walls.
De novo MN occurs in relatively late period after transplantation (102.1 ± 68.3 months), presenting various degree of proteinuria. Histological findings associated with antibody-mediated rejection (AMR), such as peritubular capillaritis and C4d deposition in peritubular capillary, were more frequently observed in the patients with de novo MN than the non-MN control patients. Donor-specific antibody (DSA) was detected in five patients at the time of biopsy. In one case of de novo MN with DSA, a donor-derived HLA was identified in the subepithelial deposits on the glomerular capillary walls combined with IgG deposition.
DSA and AMR might play some roles for the pathogenesis in some patients with de novo MN after kidney transplantation.
肾移植后新发膜性肾病(MN)的病因仍不确定。各种同种异体抗原的免疫反应被推测为病因之一。
对 17 例移植后新发 MN 患者进行临床和病理研究,并与无 MN 的移植后对照患者进行比较。通过双重免疫荧光染色来确定在肾小球毛细血管壁沉积物中是否存在与供体特异性人白细胞抗原(HLA)结合的 IgG。
新发 MN 发生在移植后相对较晚的时期(102.1±68.3 个月),表现为不同程度的蛋白尿。与抗体介导的排斥反应(AMR)相关的组织学发现,如肾小管周围毛细血管炎和肾小管周围毛细血管 C4d 沉积,在新发 MN 患者中比非 MN 对照组更常见。在活检时检测到 5 例患者存在供体特异性抗体(DSA)。在一例有 DSA 的新发 MN 中,在肾小球毛细血管壁的上皮下沉积物中鉴定出供体来源的 HLA 与 IgG 沉积相结合。
DSA 和 AMR 可能在一些肾移植后新发 MN 患者的发病机制中发挥作用。