Evidence map›Paper›PMID 29479351›Full record

ReviewFrontiers in immunology2018

T-Cell Metabolism in Hematopoietic Cell Transplantation.

Hung D Nguyen, Sandeepkumar Kuril, David Bastian, Xue-Zhong Yu

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.3field-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

24 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Observational
  16. Article
  17. T-Cell Metabolism in GraftFrontiers in immunology · 2021
    Review
  18. Article
  19. Review
  20. T cell metabolism in graft-versus-host disease.Blood science (Baltimore, Md.) · 2020
    Review
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

4 authors at 1 institution in 1 country.

Hung D NguyenDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, United States.
Sandeepkumar KurilDepartment of Pediatric Ematology-Oncology, Medical University of South Carolina, Charleston, SC, United States.
David BastianDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, United States.
Xue-Zhong YuDepartment of Microbiology and Immunology, Medical University of South Carolina, Charleston, SC, United States.
Medical University of South Carolina · US

Funding

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
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
Control of GVHD and Leukemia Relapse by Targeting Cell MetabolismR21CA192202 · NCI · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI YU, XUE-ZHONG · 2015 to 2016
$358k
NCI NIH HHS R01 CA118116NCI NIH HHS R01 CA169116NCI NIH HHS R21 CA192202NIAID NIH HHS R01 AI118305
6 · The paper itself

Abstract

Metabolism, including catabolism and anabolism, is a basic cellular process necessary for cell survival. T lymphocytes have a distinct metabolism that can determine both fate and function. T-cell activation depends on glycolysis to obtain materials and energy for proliferation and effector function. Importantly, T cells utilize different metabolic processes under different conditions and diseases. Allogeneic hematopoietic cell transplantation (allo-HCT) is a classic immunotherapy for hematological malignancies; however, the development of graft-versus-host disease (GVHD) is a major factor limiting the success of allo-HCT. T cells in the donor graft drive GVHD by mounting a robust immunological attack against recipient normal tissues. Hence, understanding T-cell metabolism after allo-HCT would provide potential metabolic targets for the control of GVHD and primary tumor relapse. The purpose of the current review is to highlight the key metabolic pathways involved in alloantigen-activated T cells and to discuss how manipulating these pathways can serve as potential new therapeutic strategies to induce immune tolerance after allo-transplantation. We will also summarize the recent progress in regulating T-cell metabolism in bone marrow transplantation by targeting novel metabolic regulators or immune checkpoint molecules.

Indexed as

Hematopoietic Stem Cell TransplantationLymphocyte ActivationGlycolysisGraft vs Host DiseaseHematologic NeoplasmsHumansImmune ToleranceMetabolic Networks and PathwaysT-Lymphocytesglycolysisgraft-versus-host diseasehematopoietic stem cell transplantationmetabolismT cell

Identifiers

PMID29479351
PMCPMC5811499
OpenAlexW2793274176

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.