Histologic findings of antibody-mediated rejection in ABO blood-group-incompatible living-donor kidney transplantation

被引:70
作者
Fidler, ME
Gloor, JM [1 ]
Lager, DJ
Larson, TS
Griffin, MD
Textor, SC
Schwab, TR
Prieto, M
Nyberg, SL
Ishitani, MB
Grande, JP
Kay, PA
Stegall, MD
机构
[1] Mayo Clin & Mayo Fdn, Dept Internal Med, Div Nephrol, Rochester, MN 55905 USA
[2] Mayo Clin & Mayo Fdn, Dept Lab Med, Div Anat Pathol, Rochester, MN 55905 USA
[3] Mayo Clin & Mayo Fdn, Dept Surg, Div Transplantat, Rochester, MN 55905 USA
关键词
ABO blood group; antibodies; blood group incompatibility; graft rejection; kidney transplant;
D O I
10.1046/j.1600-6135.2003.00278.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
The purpose of this study was to characterize the histology of antibody- mediated rejection (AMR) in ABO blood- group- incompatible (ABOI) kidney transplants as well as on protocol biopsies performed at the time of stable allograft function. Between 5/ 99 and 1/ 02, we performed 32 ABOI kidney transplants (13 A2, 19 non- A2 blood- group living donors). Nineteen biopsies were performed for allograft dysfunction, and 127 protocol biopsies were performed 0, 3, 7, 14, 28 days and 3 and 12 months post transplant. Twenty- five of 32 patients have functioning allografts (mean 585 days post transplant). Nine of 32 (28%) developed clinical AMR. Biopsy revealed glomerular thrombi (78%), mesangiolysis (78%), peritubular capillary C4d staining (56%) and neutrophil infiltration (67%), interstitial hemorrhage and necrosis (56%) and arteriolar thrombi (33%). Subclinical AMR was diagnosed by protocol biopsies in four patients. Findings consisted of glomerular thrombi (100%), mesangiolysis (25%), and C4d staining (100%). In late protocol biopsies performed 214420 days post transplant, mild mesangiolysis was seen in 2/ 17 (11.7%), and C4d immunostaining was detected in 3/ 12 (25%). AMR is characterized by glomerular thrombi, mesangiolysis, peritubular capillary neutrophil infiltration interstitial hemorrhage, necrosis, and C4d deposition. Glomerular thrombi appear early in AMR and may appear prior to graft dysfunction.
引用
收藏
页码:101 / 107
页数:7
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