Effect of recipient gender and donor-specific antibodies on antibody-mediated rejection after heart transplantation.

alloantibody clinical research/practice crossmatch gender heart transplantation/cardiology rejection: acute rejection: antibody-mediated (ABMR)

Journal

American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons
ISSN: 1600-6143
Titre abrégé: Am J Transplant
Pays: United States
ID NLM: 100968638

Informations de publication

Date de publication:
04 2019
Historique:
received: 25 02 2018
revised: 21 08 2018
accepted: 23 09 2018
pubmed: 5 10 2018
medline: 22 7 2020
entrez: 5 10 2018
Statut: ppublish

Résumé

Gender-difference regarding antibody-mediated rejection (AMR) after heart transplantation has been described. However, no study accounted for the presence of preformed donor-specific antibodies (pfDSA), a known risk factor of AMR, more common among women than men. In a single-institution 6-year cohort (2010-2015), time to AMR was assessed, comparing men with women by survival analysis with a 1-year death-censored follow-up. All AMRs were biopsy proven. Confounding variables that were accounted for included mean intensity fluorescence (MFI) of pfDSA, recipient age, HLA-, size- and sex-mismatch. 463 patients were included. Overall incidence of AMR was 10.3% at 1 year. After adjusting for confounding variables, independent risk factors of AMR were female recipient gender (adjusted hazard-ratio [adj. HR] = 1.78 [1.06-2.99]), P = .03) and the presence of pfDSA (adj. HR = 3.20 [1.80-5.70], P < .001). This association remained significant when considering pfDSA by their MFI; female recipient gender had an adj. HR = 2.2 (P = .026) and MFI of pfDSA (per 1 MFI-increase) adj. HR = 1.0002 (P < .0001). In this cohort, women were at higher risk of AMR than men and this risk increase was additive to that of pfDSA. These findings may suggest a gender-related difference in the severity of pfDSA.

Identifiants

pubmed: 30286278
doi: 10.1111/ajt.15133
pii: S1600-6135(22)09038-4
doi:

Substances chimiques

Isoantibodies 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1160-1167

Informations de copyright

© 2018 The American Society of Transplantation and the American Society of Transplant Surgeons.

Auteurs

Lee S Nguyen (LS)

APHP, Pitié-Salpétrière, Sorbonne University, Cardiac Surgery Department, Institute of Cardiology, Paris, France.
APHP, Pitié-Salpétrière, Sorbonne University, Center of Clinical Investigation, ICAN, Paris, France.

Guillaume Coutance (G)

APHP, Pitié-Salpétrière, Sorbonne University, Cardiac Surgery Department, Institute of Cardiology, Paris, France.

Joe-Elie Salem (JE)

APHP, Pitié-Salpétrière, Sorbonne University, Center of Clinical Investigation, ICAN, Paris, France.
Department of Medicine, Clinical Pharmacology, Cardio-oncology, Vanderbilt University Medical Center, Nashville, Tennessee.

Salima Ouldamar (S)

APHP, Pitié-Salpétrière, Sorbonne University, Cardiac Surgery Department, Institute of Cardiology, Paris, France.

Guillaume Lebreton (G)

APHP, Pitié-Salpétrière, Sorbonne University, Cardiac Surgery Department, Institute of Cardiology, Paris, France.

Alain Combes (A)

APHP, Pitié-Salpétrière, Sorbonne University, Intensive Care Medicine Department, ICAN, Paris, France.

Julien Amour (J)

APHP, Pitié-Salpétrière, Sorbonne University, Anesthesiology & Critical Care Medicine Department, Paris, France.

Mojgan Laali (M)

APHP, Pitié-Salpétrière, Sorbonne University, Cardiac Surgery Department, Institute of Cardiology, Paris, France.

Pascal Leprince (P)

APHP, Pitié-Salpétrière, Sorbonne University, Cardiac Surgery Department, Institute of Cardiology, Paris, France.

Shaida Varnous (S)

APHP, Pitié-Salpétrière, Sorbonne University, Cardiac Surgery Department, Institute of Cardiology, Paris, France.

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