Evidence map›Paper›PMID 40902074›Full record

ReviewBlood advances2025

Harmonized immune recovery monitoring after HCT: evidence and practical guidance from the Westhafen Intercontinental Group.

Taymour Hammoudi, Silvia Nucera, Alexandre G Troullioud Lucas, Marc Ansari, Adriana Balduzzi, Alice Bertaina, Jochen Buechner, Selim Corbacioglu, Jean-Hugues Dalle, Krzystof Kalwak and 17 more

Abstract readReview
In one paragraph

Review in Blood advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Beyond tumor biology: nursing interventions for psychological and immune health in cancer patients.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors.

Taymour HammoudiDepartment of Pediatrics, Section of Hematology, Oncology, Bone Marrow Transplant Cellular Therapeutics, University of Colorado Anschutz Medical Campus, Aurora, CO.ORCID 0000-0002-9886-8750
Silvia NuceraPediatric Department, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico San Gerardo dei Tintori, Monza, Italy.ORCID 0000-0001-9489-142X
Alexandre G Troullioud LucasDepartment of Pediatrics, Transplantation and Cellular Therapy, MSK Kids, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-1526-022X
Marc AnsariDepartment of Pediatrics, Gynecology and Obstetrics, Cansearch Research Platform for Pediatric Oncology and Hematology, Faculty of Medicine, University of Geneva, Geneva, Switzerland.ORCID 0000-0002-9649-6498
Adriana BalduzziPediatric Department, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico San Gerardo dei Tintori, Monza, Italy.ORCID 0000-0002-5879-0610
Alice BertainaDivision of Hematology, Oncology, Stem Cell Transplantation and Regenerative Medicine, Department of Pediatrics, Stanford University School of Medicine, Stanford, CA.ORCID 0000-0002-3729-436X
Jochen BuechnerDepartment of Pediatric Hematology and Oncology, Oslo University Hospital, Oslo, Norway.ORCID 0000-0001-5848-4501
Selim CorbaciogluDepartment of Pediatric Hematology, Oncology and Stem Cell Transplantation, Children's Hospital Regensburg, University of Regensburg, Regensburg, Germany.ORCID 0000-0003-1070-8486
Jean-Hugues DallePaediatric Haematology and Immunology Department, Robert-Debré Academic Hospital, Groupe Hospitalier Universitaire Assistance Publique-Hôpitaux de Paris Nord, Université Paris Cité, Paris, France.
Krzystof KalwakDepartment of Pediatric Hematology/Oncology and Bone Marrow Transplantation, Wroclaw Medical University, Wroclaw, Poland.ORCID 0000-0003-1174-5799
Dean LeeCenter for Childhood Cancer and Blood Diseases, Nationwide Children's Hospital, The Ohio State University, Columbus, OH.ORCID 0000-0001-6693-5392
John E LevineThe Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY.ORCID 0000-0002-5611-7828
Caroline A LindemansPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0002-3984-5620
Franco LocatelliDepartment of Oncology-Haematology, and Cell and Gene Therapy, Bambino Gesù Children's Hospital, Istituto di Ricovero e Cura a Carattere Scientifico, Rome, Italy.ORCID 0000-0002-7976-3654
Roland MeiselDivision of Pediatric Stem Cell Therapy, Department of Pediatric Oncology, Hematology and Clinical Immunology, Medical Faculty, Heinrich-Heine-University, Duesseldorf, Germany.
Stefan NierkensPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.
Giorgio OttavianoPediatric Department, Fondazione Istituto di Ricovero e Cura a Carattere Scientifico San Gerardo dei Tintori, Monza, Italy.ORCID 0000-0003-3777-0394
Antonio Perez-MartinezPediatric Hemato-Oncology Unit, Hospital Universitario La Paz, Madrid, Spain.
Herbert PichlerDepartment of Pediatrics and Adolescent Medicine, St Anna Children's Hospital, Medical University of Vienna, Vienna, Austria.ORCID 0000-0001-5107-5123
Susan E ProckopDana Farber/Boston Children's Hospital Center for Cancer and Blood Disorders, Boston, MA.ORCID 0000-0003-4175-5728
Michael A PulsipherHuntsman Cancer Institute/Intermountain Primary Children's Hospital, Spencer Fox Eccles School of Medicine, University of Utah, Salt Lake City, UT.ORCID 0000-0003-3030-8420
Julie-An M TalanoDepartment of Pediatric Hematology/Oncology and Bone Marrow Transplantation, Medical College of Wisconsin, Milwaukee, WI.
Sanjay TewariDepartment of Paediatric Oncology/Haematology, Royal Marsden NHS Foundation Trust Sutton, Sutton, United Kingdom.
Kirk R SchultzMichael Cuccione Cancer Research Program, BC Children's Hospital Research Institute/University of British Columbia, Vancouver, BC, Canada.ORCID 0000-0002-0001-6438
Nirali N ShahPediatric Oncology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD.ORCID 0000-0002-8474-9080
Michael R VernerisDepartment of Pediatrics, Section of Hematology, Oncology, Bone Marrow Transplant Cellular Therapeutics, University of Colorado Anschutz Medical Campus, Aurora, CO.ORCID 0000-0002-7097-5917
Jaap Jan BoelensDepartment of Pediatrics, Transplantation and Cellular Therapy, MSK Kids, Memorial Sloan Kettering Cancer Center, New York, NY.ORCID 0000-0003-2232-6952

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI SELWYN M VICKERS · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

abstractAllogeneic hematopoietic cell transplantation (allo-HCT) is a curative option for patients with high-risk malignancies and nonmalignant disorders. Long-term survival depends on robust immune reconstitution (IR), which governs overall immune homeostasis and risks of infection, graft-versus-host disease, and relapse. However, despite its centrality to posttransplant outcomes, IR is not consistently monitored across transplant centers, limiting ability to generate meaningful, comparable, and translatable data. This review synthesizes current knowledge on numerical and functional IR milestones after allo-HCT, with a primary focus on flow cytometry-based monitoring of key immune cell subsets. Importantly, early CD4+ T-cell recovery (achieving >50 cells per μL by day 100 after transplant), is supported by strong clinical evidence and correlates with improved outcomes. Although emerging data suggest that additional subsets (CD8+ T cells, natural killer cells, B cells, naïve and recent thymic emigrant T cells, and γδ T cells) may also influence clinical trajectories, further harmonized, multicenter studies are needed to validate prognostic relevance across transplant settings. We propose practical, evidence-based guidelines for IR monitoring, including recommended time points, preferred assays, and flow cytometry panel components. Additionally, we highlight modifiable factors (eg, immunosuppressive drug exposures, graft manipulation) offering interventional opportunities for influencing IR. Harmonized monitoring strategies will support robust correlation between IR and clinical outcomes, guide real-time risk stratification, and facilitate the development of targeted, individualized transplant approaches. Standardization efforts led by consortia and registries are essential for advancing knowledge and optimizing care. We provide a roadmap for implementing uniform IR monitoring to improve outcomes and quality of life for allo-HCT recipients.

Indexed as

Hematopoietic Stem Cell TransplantationImmune ReconstitutionGraft vs Host DiseaseHumansMonitoring, ImmunologicTransplantation, Homologous

Identifiers

PMID40902074
PMCPMC12719163

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.