HLA evolutionary divergence score after donor lymphocyte infusion following allogeneic hematopoietic stem cell transplantation
Donor lymphocyte infusion (DLI) prevents acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS) relapses following hematopoietic stem cell transplantation. Given the life-threatening toxicities such as graft versus host disease (GVHD), the identification of variables associated with response without toxicities is warranted. We hypothesized that HLA evolutionary divergence (HED), defined by the diversity between two given alleles of the same HLA gene, may be such a factor. A retrospective multicenter case-control study was conducted to evaluate the outcomes of pre-emptive (preDLI) and prophylactic DLI (proDLI) regarding their HED score, in AML or MDS patients. DLI-treated patients were matched with controls (1:2 matched) from French transplantation centers according to hospital, hemopathy, donor type, and risk classification. In total, 201 patients were included (<i>N</i> = 147 in the preDLI group, <i>N</i> = 54 in the proDLI group). Relapse-free survival was significantly better in the preDLI group (hazard ratio [HR] = 0.23, 95% confidence interval [CI]: 0.14-0.55, <i>p</i> < 0.001) than in controls. However, this benefit was offset by a higher incidence of severe GVHD (HR = 4.88, 95% CI: 2.30-10.32, <i>p</i> < 0.001). HED A, B, C, DQA1, DQB1, DPB1, and DRB1 were calculated for 65 DLI-treated patients. High-class II HED was significantly associated with higher GVHD and relapse-free survival (GRFS, HR = 0.33, 95% CI: 0.20-0.77, <i>p</i> = 0.005). Specific DQAB associations directly improved GRFS (HR = 0.23, 95% CI: 0.09-0.58, <i>p</i> = 0.004). In conclusion, screening the class II HED score identifies patients eligible for DLI treatment who will benefit the most from this strategy.
Authors
- Sophie Caillat‐Zucman (ORCID: https://orcid.org/0000-0002-4535-3550)
- Éric Delabesse (ORCID: https://orcid.org/0000-0002-0928-0753)
- Christian Récher (ORCID: https://orcid.org/0000-0002-3332-4525)
- Juliette Villemonteix (ORCID: https://orcid.org/0000-0002-6601-7820)
- Sophie Le Grand (ORCID: https://orcid.org/0000-0002-9985-465X)
- Véronique Mansat‐De Mas (ORCID: https://orcid.org/0000-0003-1878-9129)
- Étienne Daguindau (ORCID: https://orcid.org/0000-0001-7375-5656)
- David Michonneau (ORCID: https://orcid.org/0000-0003-4553-3065)
- Nicolas Vallet (ORCID: https://orcid.org/0000-0001-9568-3358)
- Anne Dormoy
- Vincent Allain (ORCID: https://orcid.org/0000-0002-1068-7892)
- Régis Peffault de Latour (ORCID: https://orcid.org/0000-0001-6222-4753)
- Sarah Guenounou (ORCID: https://orcid.org/0000-0002-4561-2591)
- Marylise Fort
- Anne Huynh
Institutions
- Université de Tours (FR)
- Université Toulouse III - Paul Sabatier (FR)
- Inserm (FR)
- Université Fédérale de Toulouse Midi-Pyrénées (FR)
- Université Paris Cité (FR)
- Centre Hospitalier Universitaire de Toulouse (FR)
- Centre Hospitalier Universitaire de Tours (FR)
- Hôpital Privé Jean Mermo (FR)
- Établissement Français du Sang (FR)
- Hôpital Saint-Louis (FR)
Publication Details
- Journal
- HemaSphere
- Published
- 2025-02-01
- DOI
- https://doi.org/10.1002/hem3.70088
- Citations
- 5
- Primary Topic
- Hematopoietic Stem Cell Transplantation
- Type
- article
- Field-Weighted Citation Impact
- 8.85