Evidence map›Paper›PMID 40315369›Full record

ArticleBlood advances2025

Impact of shared HLA determinants between patient and losing cord blood unit on relapse after double cord blood transplantation.

Robert Wynn, Fernanda Volt, Philippe Guardiola, Srividhya Senthil, Graziana Scigliuolo, Chantal Kenzey, Barbara Cappelli, Annalisa Ruggeri, Ryad Tamouza, Vanderson Rocha and 10 more

Abstract readMulticenter Study
In one paragraph

Article in Blood advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
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  3. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors.

Robert WynnBMT Programme, Royal Manchester Children's Hospital, Manchester, United Kingdom.ORCID 0000-0002-6046-8428
Fernanda VoltEurocord, Hôpital Saint Louis Assistance Publique-Hôpitaux de Paris, Institut de Recherche de Saint Louis EA3518, Université de Paris Cité, Paris, France.
Philippe GuardiolaEurocord, Hôpital Saint Louis Assistance Publique-Hôpitaux de Paris, Institut de Recherche de Saint Louis EA3518, Université de Paris Cité, Paris, France.
Srividhya SenthilBMT Programme, Royal Manchester Children's Hospital, Manchester, United Kingdom.
Graziana ScigliuoloEurocord, Hôpital Saint Louis Assistance Publique-Hôpitaux de Paris, Institut de Recherche de Saint Louis EA3518, Université de Paris Cité, Paris, France.
Chantal KenzeyEurocord, Hôpital Saint Louis Assistance Publique-Hôpitaux de Paris, Institut de Recherche de Saint Louis EA3518, Université de Paris Cité, Paris, France.
Barbara CappelliEurocord, Hôpital Saint Louis Assistance Publique-Hôpitaux de Paris, Institut de Recherche de Saint Louis EA3518, Université de Paris Cité, Paris, France.
Annalisa RuggeriEurocord, Hôpital Saint Louis Assistance Publique-Hôpitaux de Paris, Institut de Recherche de Saint Louis EA3518, Université de Paris Cité, Paris, France.
Ryad TamouzaUniv Paris Est Créteil, INSERM U955, Créteil, France.
Vanderson RochaEurocord, Hôpital Saint Louis Assistance Publique-Hôpitaux de Paris, Institut de Recherche de Saint Louis EA3518, Université de Paris Cité, Paris, France.ORCID 0000-0003-0094-619X
Chloe AnthiasDepartment of Bone Marrow Transplant, Royal Marsden Hospital National Health Service Trust, London, United Kingdom.
Régis Peffault de la TourDepartment de Hematologie, Hôpital Saint Louis Assistance Publique-Hôpitaux de Paris, Paris, France.
Katherine CleshamDepartment of Bone Marrow Transplant, Royal Free and University College Medical School, London, United Kingdom.
Anna CastletonDepartment of Bone Marrow Transplant, Christie National Health Service Trust Hospital, Manchester, United Kingdom.ORCID 0000-0002-5798-8692
Michel SchaapDepartment of Bone Marrow Transplant, Radboud University Medical Centre, Nijmegen, The Netherlands.ORCID 0000-0001-7696-4752
Persis AmroliaDepartment of Bone Marrow Transplant, Great Ormond Street Hospital for Children Natoinal Health Service Foundation Trust, London, United Kingdom.ORCID 0000-0003-0480-3911
Marc BieringsDepartment of Bone Marrow Transplant, Princess Máxima Center, Utrecht, The Netherlands.ORCID 0000-0002-0192-3080
Jan J CornelissenDepartment of Hematology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Kay PoultonTransplantation Laboratory, Manchester National Health Service Foundation Trust, Manchester, United Kingdom.ORCID 0000-0002-5608-8107
Eliane GluckmanEurocord, Hôpital Saint Louis Assistance Publique-Hôpitaux de Paris, Institut de Recherche de Saint Louis EA3518, Université de Paris Cité, Paris, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractDuring double umbilical cord blood transplant (DUCBT), the winning unit (WU) rejects the losing unit (LU) because of WU T cells directed against the LU mismatched HLA. This immune response might protect against relapse, especially when the patient and LU (PT-LU) share the same mismatch with the WU. To validate this hypothesis, a retrospective Eurocord study, conducted on 383 DUCBTs, focused on posttransplant relapse and HLA mismatches between PT-LU and the WU. A PT-LU HLA-A mismatch shared with the WU was associated with a lower 7-year relapse incidence (16% vs 28%; P = .048). In addition, multiple PT-LU shared HLA mismatches were also associated with a lower relapse risk (7% vs 29%; P = .003). In DUCBT with ≥2 HLA mismatches between patient and WU, the number of HLA mismatches between those did not significantly affect relapse incidence, whereas multiple PT-LU shared HLA mismatches remained associated with a lower relapse risk (7% vs 29%; P = .0038). Finally, considering patients who did not develop either grade 2 to 4 acute graft-versus-host disease or chronic graft-versus-host disease, a PT-LU shared HLA-A mismatch as well as multiple PT-LU HLA mismatches shared with the WU remained associated with a significantly lower 7-year relapse incidence. In multivariate adjusted analyses multiple PT-LU shared HLA mismatches remained associated with a significantly reduced 7-year posttransplant relapse risk. Our analysis indicates that, during DUCBT, PT-LU shared HLA mismatches prime an immune response of the WU against leukemia, reducing the long-term risk of posttransplant relapse, and that DCBT has particular utility in those with high-risk leukemia.

Indexed as

Cord Blood Stem Cell TransplantationGraft vs Host DiseaseHLA AntigensLeukemiaMyelodysplastic SyndromesAdolescentAdultAgedChildChild, PreschoolFemaleFollow-Up StudiesHistocompatibility TestingHumansIncidenceMaleHLA Antigens

Identifiers

PMID40315369
PMCPMC12405680

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.