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Differences in pathologic features and graft outcomes in antibody-mediated rejection of renal allografts due to persistent/recurrent versus de novo donor-specific antibodies.
Haas, Mark; Mirocha, James; Reinsmoen, Nancy L; Vo, Ashley A; Choi, Jua; Kahwaji, Joseph M; Peng, Alice; Villicana, Rafael; Jordan, Stanley C.
Affiliation
  • Haas M; Department of Pathology and Laboratory Medicine, Cedars-Sinai Medical Center, Los Angeles, California, USA. Electronic address: mark.haas@cshs.org.
  • Mirocha J; Biostatistics Core, Research Institute and General Clinical Research Center, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Reinsmoen NL; HLA and Immunogenetics Laboratory, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Vo AA; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Choi J; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Kahwaji JM; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Peng A; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, California, USA.
  • Villicana R; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, California, USA; Transplantation Institute, Loma Linda University Medical Center, Loma Linda, California, USA.
  • Jordan SC; Comprehensive Transplant Center, Cedars-Sinai Medical Center, Los Angeles, California, USA.
Kidney Int ; 91(3): 729-737, 2017 03.
Article in En | MEDLINE | ID: mdl-28104301
ABSTRACT
Antibody-mediated rejection (ABMR) of renal allografts occurs in two forms. Type 1 ABMR results from persistence and/or a rebound of preexisting donor-specific antibodies in sensitized patients and usually occurs early post-transplantation. Type 2 ABMR is associated with de novo donor-specific antibodies and usually occurs over one year post-transplantation. It is generally accepted that types 1 and 2 also differ with regard to certain pathologic features including the frequencies of C4d positivity and concurrent cell-mediated rejection. However, direct comparison of pathologic, serologic, and clinical features of types 1 and 2 ABMR is lacking. Here we compared these features in 80 cases of ABMR (37 type 1, 43 type 2) diagnosed at our center. Compared with type 1, type 2 ABMR occurred later post-transplantation, was more often associated with donor-specific antibodies against Class II HLA, and was associated with more interstitial fibrosis/tubular atrophy and more frequent cell-mediated rejection, although these did not differ with respect to C4d positivity. By univariate analysis, graft survival was lower with type 2 than type 1 ABMR with borderline significance. Still, among these 80 patients, all but one treated for ABMR following diagnosis, the only two independent predictors of graft failure were at least moderate interstitial fibrosis/tubular atrophy and failure of the donor-specific antibody relative intensity scale score, a measure of the combined strength of all donor-specific antibodies present, to decrease in response to therapy.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Kidney Transplantation / Graft Rejection / Graft Survival / HLA Antigens / Isoantibodies / Kidney Type of study: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Country/Region as subject: America do norte Language: En Journal: Kidney Int Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Kidney Transplantation / Graft Rejection / Graft Survival / HLA Antigens / Isoantibodies / Kidney Type of study: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Middle aged Country/Region as subject: America do norte Language: En Journal: Kidney Int Year: 2017 Document type: Article