Evidence map›Paper›PMID 27722210›Full record

ArticleJournal of immunology research and therapy2016

Regulatory T-Cell Therapy for Graft-versus-host Disease.

Jessica Heinrichs, David Bastian, Anandharaman Veerapathran, Claudio Anasetti, Brain Betts, Xue-Zhong Yu

Open access · greenAbstract read
In one paragraph

Article in Journal of immunology research and therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.8field-weighted citation impact, top 8% of its field
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

25 citing papers in PubMed, 39 citations in OpenAlex.

  1. Orca-T: First Approval.Molecular diagnosis & therapy · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Regulatory T Cells in GVHD Therapy.Frontiers in immunology · 2021
    Review
  8. Article
  9. [Genetically modified regulatory T cells: therapeutic concepts and regulatory aspects].Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz · 2020
    Review
  10. Immune Pathogenesis of COVID-19 Intoxication: Storm or Silence?Pharmaceuticals (Basel, Switzerland) · 2020
    Review
  11. Article
  12. Review
  13. Article
  14. The promise of CD4Haematologica · 2019
    Review
  15. Article
  16. Article
  17. Very Low Numbers of CD4Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2018
    Article
  18. Review
  19. Article
  20. Article
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

6 authors at 1 institution in 1 country.

Jessica HeinrichsDepartment of Microbiology & Immunology, Medical University of South Carolina, Charleston, SC, USA; Department of Pathology and Cell Biology, College of Medicine, University of South Florida, USA.
David BastianDepartment of Microbiology & Immunology, Medical University of South Carolina, Charleston, SC, USA.
Anandharaman VeerapathranDepartment of Blood & Marrow Translation, Moffitt Cancer Center, Tampa, FL, USA.
Claudio AnasettiDepartment of Blood & Marrow Translation, Moffitt Cancer Center, Tampa, FL, USA.
Brain BettsDepartment of Blood & Marrow Translation, Moffitt Cancer Center, Tampa, FL, USA.
Xue-Zhong YuDepartment of Microbiology & Immunology, Medical University of South Carolina, Charleston, SC, USA; Division of Hematology/Oncology, Department of Medicine, Medical University of South Carolina, Charleston, SC, USA.
Medical University of South Carolina · US

Funding

South Carolina Clinical & Translational Research Institute (SCTR)UL1TR001450 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI BRADY, KATHLEEN T., FLUME, PATRICK A · 2015 to 2024
$41.1M
South Carolina Clinical & Translational Research Institute (SCTR)TL1TR001451 · NCATS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI FEGHALI-BOSTWICK, CAROL A. · 2015 to 2024
$4.6M
Role of Inflammation in tumor promotion and progressionR01CA118165 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KARIN, MICHAEL · 2007 to 2016
$4.6M
GENETIC ANALYSIS OF AGING IN C ELEGANSR01AG011816 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ASHRAFI, KAVEH · 1994 to 2018
$3.6M
Effects of Foxp3-Induced Regulatory T Cells on GVHD and GVT ActivityR01CA118116 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI YU, XUE-ZHONG · 2006 to 2015
$2.2M
Elucidating the Function of PKC-theta in Alloreactivity and GVHDR01AI082685 · NIAID · H. LEE MOFFITT CANCER CTR & RES INST · PI BEG, AMER AZIZ, YU, XUE-ZHONG · 2010 to 2014
$2.0M
MicroRNA Regulates Graft-versus-Host DiseaseR01AI118305 · NIAID · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI YU, XUE-ZHONG · 2015 to 2019
$1.7M
Targeting IL-12/23 p40 Pathways for the Control of GVHDR01CA169116 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI YU, XUE-ZHONG · 2013 to 2017
$1.6M
Th1/Th17 Cell Differentiation in GVHD and GVLR01CA143812 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI YU, XUE-ZHONG · 2010 to 2013
$1.3M
NCATS NIH HHS TL1 TR001451NCATS NIH HHS UL1 TR001450NCI NIH HHS R01 CA118116NCI NIH HHS R01 CA118165NCI NIH HHS R01 CA143812NCI NIH HHS R01 CA169116NIAID NIH HHS R01 AI082685NIAID NIH HHS R01 AI118305NIA NIH HHS R01 AG011816United States NCIUnited States NIAID
6 · The paper itself

Abstract

Graft-versus-host disease (GVHD) is a significant cause of non-relapse mortality after allogeneic hematopoietic cell transplantation (allo-HCT). Existing strategies to prevent and treat GVHD are incomplete, where a significant portion of allo-HCT recipients developed this complication. Despite this, one such therapy has emerged involving the use of regulatory T cells (Tregs) to control GVHD. The use of natural Tregs (nTregs) yielded positive pre-clinical results and are actively under investigation to reduce GVHD. However, broad application of this approach may require standardization of Treg expansion methods and dosing. Inducible Tregs (iTregs) can be seamlessly generated, but controversial pre-clinical findings and phenotype instability have hampered their translation into the clinic. Here, we review the current biological differences between nTregs and iTregs, as well as their effects on GVHD and graft-versus-leukemia (GVL) responses. We conclude by exploring the idea of combinational cellular therapies for the prevention of GVHD and preservation of GVL.

Indexed as

Cellular therapyGraft-versus-host disease (GVHD)iTregsnTregs

Identifiers

PMID27722210
PMCPMC5049884
OpenAlexW2531682663

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.