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Utility of Routine Post Kidney Transplant Anti-HLA Antibody Screening.
Salhi, Sofiane; Congy-Jolivet, Nicolas; Hebral, Anne-Laure; Esposito, Laure; Vieu, Guillaume; Milhès, Jean; Kamar, Nassim; Del Bello, Arnaud.
Afiliación
  • Salhi S; Department of Nephrology and Organ Transplantation, CHU Rangueil, Toulouse, France.
  • Congy-Jolivet N; Faculté de santé, Université Paul Sabatier, Toulouse, France.
  • Hebral AL; Faculté de santé, Université Paul Sabatier, Toulouse, France.
  • Esposito L; Molecular Immunogenetics Laboratory, EA 3034, Faculté de Médecine Purpan, IFR150 (INSERM), France.
  • Vieu G; Department of Immunology, CHU de Toulouse, Hôpital de Rangueil, CHU de Toulouse, France.
  • Milhès J; Department of Nephrology and Organ Transplantation, CHU Rangueil, Toulouse, France.
  • Kamar N; Department of Nephrology and Organ Transplantation, CHU Rangueil, Toulouse, France.
  • Del Bello A; Etablissement Francais du Sang, CHU de Purpan, Toulouse, France.
Kidney Int Rep ; 9(5): 1343-1353, 2024 May.
Article en En | MEDLINE | ID: mdl-38707794
ABSTRACT

Introduction:

De novo donor-specific antibody (dnDSA) is a strong biomarker associated with the development of antibody-mediated rejection (AMR) and graft loss after kidney transplantation. This procedure is expensive; however, systematic annual screening was recommended by some national organ transplant agencies or societies even though its clinical utility was not clearly established.

Methods:

To address this question, we retrospectively assessed the incidence of dnDSA according to the test justification (clinically indicated or systematic) in a cohort of low-immunological risk patients, defined by being nonhuman leukocyte antigen (non-HLA)-sensitized and having no previous kidney transplants.

Results:

A total of 1072 patients, for whom 4611 anti-HLA tests were performed, were included in the study. During the follow-up period of 8 (interquartile range, IQR 5-11) years, 77 recipients developed dnDSA (prevalence of 7.2%). Thirty-five of these dnDSAs (45.5%) were detected during the first year posttransplantation. In 95% of patients with dnDSA, an immunizing event was identified in their medical records. dnDSA was detected in 46 of 4267 systematic screening tests (1.08%) performed. Active and chronic AMR were frequently observed in biopsies performed after systematic DSA testing (17.9% and 15.4%, respectively).

Conclusion:

Our results suggest that the detection by systematic screening of dnDSA in low-immunological risk kidney transplant patients without sensitizing events is a rare event, especially after 1 year. Moreover, in real life, systematic annual screening for dnDSA, seems having a limited impact to detect AMR at an earlier stage compared to patients in whom dnDSA was detected after a clinically indicated test.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Kidney Int Rep Año: 2024 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Kidney Int Rep Año: 2024 Tipo del documento: Article País de afiliación: Francia