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Sex-specific survival difference in association with HLA-DRB1∗04 following allogeneic haematopoietic stem cell transplantation for lymphoid malignancies.

Authors :
Balassa K
Andrikovics H
Remenyi P
Batai A
Szilvasi A
Bors A
Kiss KP
Rajczy K
Inotai D
Torbagyi E
Lengyel L
Barta A
Gopcsa L
Tordai A
Masszi T
Source :
Human immunology [Hum Immunol] 2018 Jan; Vol. 79 (1), pp. 13-19. Date of Electronic Publication: 2017 Oct 31.
Publication Year :
2018

Abstract

The role of HLA system in allogeneic haematopoietic stem cell transplantation (allo-HSCT) outcome is unarguable. In this study we investigated association of HLA-A,-B and-DRB1 alleles with overall survival (OS) in 186 patients undergoing allo-HSCT for lymphoid malignancies. Analyses confirmed significantly better OS for HLA-DRB1∗04 carriers compared with non-carriers (p = 0.01). Survival benefit was confined to male patients (in multivariate analyses p = 0.034, hazard ratio 0.35, 95% confidence interval 0.13-0.92), whereas in females no difference was noted (p = 0.82). Furthermore, donor gender also affected outcome and transplantation from female HLA-DRB1∗04 carrier donors resulted in superior survival compared with female non-carrier donors (p = 0.01). Combined analyses including recipient/donor gender and HLA-DRB1∗04 showed that survival of male patients varied significantly according to donor gender and HLA-DRB1∗04 carriership (p = 0.04) with best survival among HLA-DRB1∗04 carriers transplanted from female donors. Of relevance to our results, HLA-DRB1∗04 has been documented as risk allele group for lymphoid malignancies, and studies described a male-specific risk. We believe that our findings provide further supporting evidence for sex-specific alterations secondary to HLA-DRB1∗04 or related genes. Further studies are warranted to evaluate whether in contrast to general favour of male donors HLA-DRB1∗04 carrier patients with lymphoid malignancies could benefit from transplantation from female donors.<br /> (Copyright © 2017 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1879-1166
Volume :
79
Issue :
1
Database :
MEDLINE
Journal :
Human immunology
Publication Type :
Academic Journal
Accession number :
29080718
Full Text :
https://doi.org/10.1016/j.humimm.2017.10.010