Evidence map›Paper›PMID 25742699›Full record

Trial reportBlood2015

Role of naive-derived T memory stem cells in T-cell reconstitution following allogeneic transplantation.

Alessandra Roberto, Luca Castagna, Veronica Zanon, Stefania Bramanti, Roberto Crocchiolo, James E McLaren, Sara Gandolfi, Paolo Tentorio, Barbara Sarina, Inna Timofeeva and 11 more

2 registry-linked trialsAbstract readClinical Trial
In one paragraph

Trial report in Blood, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 103 papers.

0numbers the graph read from it
0cells of the map it votes in
103citing 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.

NCT02049424 terminatednot on this map

Retrospective-prospective Observational Study for Data Collection of Patients Who Underwent an Haploidentical Transplantation After Non-myeloablative Conditioning Regimen

TypeobservationalSponsorIstituto Clinico HumanitasRan2011 to 2013Enrolled9ConditionsHematologic Malignancy
NCT02049580 phase2unknown statusnot on this map

Multi-center, Phase II Study to Assess the Safety and Efficacy of Haploidentical Bone Marrow Transplantation Using Reduced Intensity Conditioning(RIC)Regimen and Post-transplant Cyclophosphamide,in Patients With Poor Prognosis Lymphomas

TypeinterventionalSponsorIstituto Clinico HumanitasRan2013 to 2016Enrolled47ConditionsLymphomaArmsThiotepa, Fludarabine, Cyclophosphamide
3 · Its place in the literature

Who cites it

103 citing papers in PubMed.

  1. Trial
  2. Trial
  3. Trial
  4. Trial
  5. Review
  6. Cytotoxic CD4Signal transduction and targeted therapy · 2026
    Review
  7. Article
  8. Review
  9. Review
  10. TNature communications · 2025
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Role of stem cell-like memory T cells in autoimmune diseases.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2023
    Article

43 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors.

Alessandra RobertoUnit of Clinical and Experimental Immunology, Humanitas Clinical and Research Center, Rozzano, Milan, Italy;ORCID http://orcid.org/0000-0001-6615-0026
Luca CastagnaHematology and Bone Marrow Transplant Unit, Humanitas Cancer Center, Rozzano, Milan, Italy;
Veronica ZanonUnit of Clinical and Experimental Immunology, Humanitas Clinical and Research Center, Rozzano, Milan, Italy;
Stefania BramantiHematology and Bone Marrow Transplant Unit, Humanitas Cancer Center, Rozzano, Milan, Italy;
Roberto CrocchioloHematology and Bone Marrow Transplant Unit, Humanitas Cancer Center, Rozzano, Milan, Italy;
James E McLarenInstitute of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom;
Sara GandolfiHematology and Bone Marrow Transplant Unit, Humanitas Cancer Center, Rozzano, Milan, Italy;
Paolo TentorioUnit of Clinical and Experimental Immunology, Humanitas Clinical and Research Center, Rozzano, Milan, Italy;
Barbara SarinaHematology and Bone Marrow Transplant Unit, Humanitas Cancer Center, Rozzano, Milan, Italy;
Inna TimofeevaHematology and Bone Marrow Transplant Unit, Humanitas Cancer Center, Rozzano, Milan, Italy;
Armando SantoroHematology and Bone Marrow Transplant Unit, Humanitas Cancer Center, Rozzano, Milan, Italy;
Carmelo Carlo-StellaHematology and Bone Marrow Transplant Unit, Humanitas Cancer Center, Rozzano, Milan, Italy; Department of Medical Biotechnologies and Translational Medicine (BioMeTra), University of Milan, Milan, Italy;
Benedetto BrunoDepartment of Molecular Biotechnology and Health Sciences, University of Torino, Torino, Italy;
Cristiana CarnitiDepartment of Haematology and Pediatric Onco-Haematology, Istituto Nazionale Tumori, Milan, Italy; and.
Paolo CorradiniDepartment of Haematology and Pediatric Onco-Haematology, Istituto Nazionale Tumori, Milan, Italy; and.
Emma GostickInstitute of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom;
Kristin LadellInstitute of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom;
David A PriceInstitute of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom;
Mario RoedererImmunoTechnology Section, Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD.
Domenico MavilioUnit of Clinical and Experimental Immunology, Humanitas Clinical and Research Center, Rozzano, Milan, Italy; Department of Medical Biotechnologies and Translational Medicine (BioMeTra), University of Milan, Milan, Italy;ORCID http://orcid.org/0000-0001-6147-0952
Enrico LugliUnit of Clinical and Experimental Immunology, Humanitas Clinical and Research Center, Rozzano, Milan, Italy;ORCID http://orcid.org/0000-0002-1964-7678

Funding

Functional And Phenotypic Characterization Of T Cells In ManZIAAI005021 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI ROEDERER, MARIO · 2009 to 2022
$14.4M
Intramural NIH HHSWellcome Trust 100326
6 · The paper itself

Abstract

Early T-cell reconstitution following allogeneic transplantation depends on the persistence and function of T cells that are adoptively transferred with the graft. Posttransplant cyclophosphamide (pt-Cy) effectively prevents alloreactive responses from unmanipulated grafts, but its effect on subsequent immune reconstitution remains undetermined. Here, we show that T memory stem cells (TSCM), which demonstrated superior reconstitution capacity in preclinical models, are the most abundant circulating T-cell population in the early days following haploidentical transplantation combined with pt-Cy and precede the expansion of effector cells. Transferred naive, but not TSCM or conventional memory cells preferentially survive cyclophosphamide, thus suggesting that posttransplant TSCM originate from naive precursors. Moreover, donor naive T cells specific for exogenous and self/tumor antigens persist in the host and contribute to peripheral reconstitution by differentiating into effectors. Similarly, pathogen-specific memory T cells generate detectable recall responses, but only in the presence of the cognate antigen. We thus define the cellular basis of T-cell reconstitution following pt-Cy at the antigen-specific level and propose to explore naive-derived TSCM in the clinical setting to overcome immunodeficiency. These trials were registered at www.clinicaltrials.gov as #NCT02049424 and #NCT02049580.

Indexed as

Hematopoietic Stem Cell TransplantationImmunologic MemoryLymphopoiesisAdultBlood DonorsCell DifferentiationCells, CulturedCell SurvivalHumansLymphocyte CountStem CellsT-Cell Antigen Receptor SpecificityT-LymphocytesTransplantation, HomologousTransplantation Immunology

Identifiers

PMID25742699
PMCPMC4424633

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.