Revisiting Traditional Risk Factors for Rejection and Graft Loss After Kidney Transplantation

被引:166
作者
Dunn, T. B. [1 ]
Noreen, H. [2 ]
Gillingham, K. [1 ]
Maurer, D. [2 ]
Ozturk, O. G. [3 ]
Pruett, T. L. [1 ]
Bray, R. A. [3 ]
Gebel, H. M. [3 ]
Matas, A. J. [1 ]
机构
[1] Univ Minnesota, Dept Surg, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Lab Med & Pathol, Minneapolis, MN 55455 USA
[3] Emory Univ, Histocompatibil & Immunogenet Lab, Atlanta, GA 30322 USA
关键词
Antibody-mediated rejection; retransplant; risk; sensitization; ANTIBODY-MEDIATED REJECTION; CLINICAL-RELEVANCE; RENAL-TRANSPLANTATION; CROSS-MATCH; T-CELLS; CLASS-I; RETRANSPLANTATION; CLASSIFICATION; SENSITIVITY; ALLOGRAFTS;
D O I
10.1111/j.1600-6143.2011.03640.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Single-antigen bead (SAB) testing permits reassessment of immunologic risk for kidney transplantation. Traditionally, high panel reactive antibody (PRA), retransplant and deceased donor (DD) grafts have been associated with increased risk. We hypothesized that this risk was likely mediated by (unrecognized) donor-specific antibody (DSA). We grouped 587 kidney transplants using clinical history and single-antigen bead (SAB) testing of day of transplant serum as (1) unsensitized; PRA = 0 (n = 178), (2) third-party sensitized; no DSA (n = 363) or (3) donor sensitized; with DSA (n = 46), and studied rejection rates, death-censored graft survival (DCGS) and risk factors for rejection. Antibody-mediated rejection (AMR) rates were increased with DSA (p < 0.0001), but not with panel reactive antibody (PRA) in the absence of DSA. Cell-mediated rejection (CMR) rates were increased with DSA (p < 0.005); with a trend to increased rates when PRA>0 in the absence of DSA (p = 0.08). Multivariate analyses showed risk factors for AMR were DSA, worse HLA matching, and female gender; for CMR: DSA, PRA>0 and worse HLA matching. AMR and CMR were associated with decreased DCGS. The presence of DSA is an important predictor of rejection risk, in contrast to traditional risk factors. Further development of immunosuppressive protocols will be facilitated by stratification of rejection risk by donor sensitization.
引用
收藏
页码:2132 / 2143
页数:12
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