Early Versus Late Acute Antibody-Mediated Rejection in Renal Transplant Recipients

被引:72
作者
Dorje, Christina [1 ]
Midtvedt, Karsten [1 ]
Holdaas, Hallvard [1 ]
Naper, Christian [2 ]
Strom, Erik H. [3 ]
Oyen, Ole [1 ]
Leivestad, Torbjorn [1 ,4 ]
Aronsen, Tommy [5 ]
Jenssen, Trond [1 ,6 ]
Flaa-Johnsen, Linda [1 ]
Lindahl, Jorn Petter [1 ]
Hartmann, Anders [1 ]
Reisaeter, Anna Varberg [1 ,4 ]
机构
[1] Natl Hosp Norway, Oslo Univ Hosp, Dept Transplant Med, N-0424 Oslo, Norway
[2] Natl Hosp Norway, Oslo Univ Hosp, Inst Immunol, N-0424 Oslo, Norway
[3] Natl Hosp Norway, Oslo Univ Hosp, Dept Pathol, N-0424 Oslo, Norway
[4] Natl Hosp Norway, Oslo Univ Hosp, Norwegian Renal Registry, N-0424 Oslo, Norway
[5] Drammen Hosp, Dept Nephrol, Drammen, Norway
[6] Univ Tromso, Inst Clin Med, Tromso, Norway
关键词
Antibody-mediated rejection; Donor-specific antibodies; Graft survival; Kidney transplantation; Nonadherence; DONOR-SPECIFIC ANTIBODIES; KIDNEY-TRANSPLANT; ALLOGRAFT-REJECTION; HLA ANTIBODIES; CLASS-I; ORGAN-TRANSPLANTATION; PATHOLOGICAL FEATURES; FUTURE-DIRECTIONS; OUTCOMES; NONADHERENCE;
D O I
10.1097/TP.0b013e31829434d4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Over the last decade, the diagnostic precision for acute antibody-mediated rejection (aABMR) in kidney transplant recipients has improved significantly. The phenotypes of early and late aABMR may differ. We assessed the characteristics and outcomes of early versus late aABMR. Methods. Between January 1, 2005 and December 31, 2010, aABMR was diagnosed in 67 grafts in 65 kidney recipients, with a median follow-up of 3.6 years (range, 61 days-7.3 years). Recipients were stratified by early aABMR (<3 months after transplantation; n=40) and late aABMR (93 months after transplantation; n=27). The main outcome was kidney allograft loss. Outcome of aABMR was compared with recipients with acute early (n=276) or late (n=100) non-ABMR during the same period. Results. Recipients with late aABMR had significantly reduced graft survival compared with recipients with early aABMR (P<0.001, log-rank test; 40% vs. 75% at 4 years; hazard ratio, 3.72; 95% confidence interval, 1.65-8.42). Graft survival in late aABMR was also inferior to late non-ABMR acute rejections (P=0.008). At transplantation, more patients were presensitized to human leukocyte antigens (22 [55%] vs. 4 [15%] in the early vs. late aABMR group). The late aABMR group was characterized by younger recipient age (37.9+/-12.9 vs. 50.9+/-11.6 years; P<0.001), increased occurrence of de novo donor-specific antibodies (52% vs. 13%; P=0.001), and nonadherence/suboptimal immuno-suppression (56% vs. 0%; P<0.001). Conclusion. Compared with early aABMR, late aABMR had inferior graft survival and was characterized by young age, frequent nonadherence, or suboptimal immunosuppression and de novo donor-specific antibodies.
引用
收藏
页码:79 / 84
页数:6
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