Mother Donors Improve Outcomes after HLA Haploidentical Transplantation: A Study by the Cellular Therapy and Immunobiology Working Party of the European Society for Blood and Marrow Transplantation.


Journal

Transplantation and cellular therapy
ISSN: 2666-6367
Titre abrégé: Transplant Cell Ther
Pays: United States
ID NLM: 101774629

Informations de publication

Date de publication:
04 2022
Historique:
received: 13 07 2021
revised: 30 11 2021
accepted: 02 01 2022
pubmed: 13 1 2022
medline: 6 4 2022
entrez: 12 1 2022
Statut: ppublish

Résumé

Transplacental trafficking of maternal and fetal cells during pregnancy establishes long-term reciprocal microchimerism in both mother and child. Consequently, the maternal immune system may become sensitized to paternal histocompatibility antigens. It has been hypothesized that mother's "exposure" to paternal HLA haplotype antigens during pregnancy may affect the outcome of hematopoietic stem cell transplantation (HSCT) when the mother serves as a donor for the child. In T cell-depleted HLA haploidentical HSCT, maternal donors have been associated with improved transplantation outcomes. The present retrospective multicenter study, conducted on behalf of the Cellular Therapy and Immunobiology Working Party of the European Society of Blood and Marrow Transplantation, involved 409 patients (102 pediatric and 307 adult) with acute leukemia who underwent HLA-haploidentical HSCT. The goal of the study was to evaluate the role of maternal donors in a large cohort of haploidentical transplantation recipients. Transplantation from maternal donors was associated with a lower relapse incidence in T cell-depleted HSCTs (hazard ratio [HR], 2.13; 95% confidence interval [CI], 1.16 to 3.92; P = .018) as well as in a limited series of unmanipulated in vivo T cell-depleted HSCTs (HR, 4.15; 95% CI, 0.94 to 18.35; P = .06), along with better graft-versus-host disease/relapse-free survival (GRFS) in T cell-depleted HSCT (HR, 1.67; 95% CI, 1.02 to 2.73; P = .04). These results indicate that the mother is the preferred donor to provide better GRFS in T cell-depleted HLA-haploidentical HSCT for acute leukemia.

Identifiants

pubmed: 35017118
pii: S2666-6367(22)00001-X
doi: 10.1016/j.jtct.2022.01.001
pii:
doi:

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

206.e1-206.e6

Informations de copyright

Copyright © 2022 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

Auteurs

Loredana Ruggeri (L)

University of Perugia, Perugia, Italy. Electronic address: loredana.ruggeri@ospedale.perugia.it.

Dirk-Jan Eikema (DJ)

European Society for Blood and Marrow Transplantation Statistical Unit, Leiden, The Netherlands.

Attilio Bondanza (A)

IRCCS Ospedale San Raffaele and Università Vita-Salute San Raffaele, Milano, Italy.

Maddalena Noviello (M)

IRCCS Ospedale San Raffaele and Università Vita-Salute San Raffaele, Milano, Italy.

Anja van Biezen (A)

European Society for Blood and Marrow Transplantation Data Office, Leiden, The Netherlands.

Liesbeth C de Wreede (LC)

Department of Biomedical Data Sciences, Leiden University Medical Center, Leiden, The Netherlands.

Lara Crucitti (L)

IRCCS Ospedale San Raffaele and Università Vita-Salute San Raffaele, Milano, Italy.

Luca Vago (L)

IRCCS Ospedale San Raffaele and Università Vita-Salute San Raffaele, Milano, Italy.

Sara Ciardelli (S)

University of Perugia, Perugia, Italy.

Peter Bader (P)

Universitaetsklinikum Frankfurt Goethe-Universitaet, Frankfurt, Germany.

Yener Koc (Y)

Medicana International Hospital, Istanbul, Turkey.

Franco Locatelli (F)

IRRCS Ospedale Pediatrico Bambino Gesů, Rome, Sapienza, University of Rome, Italy.

Joan H Veelken (JH)

Leiden University Hospital, The Netherlands.

Bernd Gruhn (B)

Department of Pediatrics, Jena University Hospital, Jena, Germany.

Pamela Evans (P)

Children's Health Ireland at Crumlin, Crumlin, Dublin 12, Ireland.

Christian Chabannon (C)

Institut Paoli-Calmettes, Centre de Lutte Contre le Cancer, Centre d'Investigations Cliniques en Biothérapie, Université d'Aix-Marseille, Inserm CBT 1409, Marseille, France.

Antoine Toubert (A)

Université de Paris, Inserm U1160, Hôpital Saint-Louis, APHP, Paris, France.

Andrea Velardi (A)

University of Perugia, Perugia, Italy.

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Classifications MeSH