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Proposed Diagnostic Criteria for Chronic Antibody-Mediated Rejection in Liver Allografts.
O'Leary, J G; Cai, J; Freeman, R; Banuelos, N; Hart, B; Johnson, M; Jennings, L W; Kaneku, H; Terasaki, P I; Klintmalm, G B; Demetris, A J.
Afiliación
  • O'Leary JG; Annette C. & Harold C. Simmons Transplant Institute, Baylor University Medical Center, Dallas, TX.
  • Cai J; Terasaki Foundation Laboratory, Los Angeles, CA.
  • Freeman R; Annette C. & Harold C. Simmons Transplant Institute, Baylor University Medical Center, Dallas, TX.
  • Banuelos N; Terasaki Foundation Laboratory, Los Angeles, CA.
  • Hart B; Annette C. & Harold C. Simmons Transplant Institute, Baylor University Medical Center, Dallas, TX.
  • Johnson M; Annette C. & Harold C. Simmons Transplant Institute, Baylor University Medical Center, Dallas, TX.
  • Jennings LW; Annette C. & Harold C. Simmons Transplant Institute, Baylor University Medical Center, Dallas, TX.
  • Kaneku H; Terasaki Foundation Laboratory, Los Angeles, CA.
  • Terasaki PI; Terasaki Foundation Laboratory, Los Angeles, CA.
  • Klintmalm GB; Annette C. & Harold C. Simmons Transplant Institute, Baylor University Medical Center, Dallas, TX.
  • Demetris AJ; Department of Pathology, University of Pittsburgh, Pittsburgh, PA.
Am J Transplant ; 16(2): 603-14, 2016 Feb.
Article en En | MEDLINE | ID: mdl-26469278
ABSTRACT
Donor-specific alloantibodies (DSA) can cause acute antibody-mediated rejection (AMR) in all solid organ allografts. However, long-term outcome in patients with posttransplant DSA needs further study. We retrospectively evaluated prospectively collected paired serum, tissue, and data on 45 matched DSA- positive [DSA+; mean florescence intensity (MFI) ≥10,000] and -negative (DSA-) recipients of a primary liver-only allograft from January 2000 to April 2009. Blinded histopathologic evaluation demonstrated that DSA+ versus DSA- patients were more likely to have subtle inflammation and unique patterns of fibrosis, despite normal or near-normal liver function tests. Stepwise multivariable modeling developed a score (putatively named the chronic AMR [cAMR] score) that included interface activity, lobular inflammation, portal tract collagenization, portal venopathy, sinusoidal fibrosis, and hepatitis C virus status. The score was developed (c = 0.811) and cross-validated (c = 0.704) to predict allograft failure. Two cutoffs were employed to optimize sensitivity and specificity (80% each); a value >27.5 predicted 50% 10-year allograft failure. We propose chronic AMR as a potential new entity defined by (1) a high cAMR score, (2) DSA, and (3) elimination of other potential causes of a similar injury pattern. In conclusion, cAMR score calculation identified liver allograft recipients with DSA at highest risk for allograft loss, although independent validation is needed.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Complicaciones Posoperatorias / Trasplante de Hígado / Enfermedad Hepática en Estado Terminal / Rechazo de Injerto / Isoanticuerpos Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Am J Transplant Asunto de la revista: TRANSPLANTE Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Complicaciones Posoperatorias / Trasplante de Hígado / Enfermedad Hepática en Estado Terminal / Rechazo de Injerto / Isoanticuerpos Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Am J Transplant Asunto de la revista: TRANSPLANTE Año: 2016 Tipo del documento: Article