Evidence map›Paper›PMID 24517424›Full record

ReviewImmunological reviews2014

The complex and central role of interferon-γ in graft-versus-host disease and graft-versus-tumor activity.

Hui Wang, Yong-Guang Yang

Abstract readReview
In one paragraph

Review in Immunological reviews, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

41 citing papers in PubMed, 57 citations in OpenAlex.

  1. Trial
  2. CD56Haematologica · 2017
    Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Human CD4iScience · 2024
    Article
  9. Clinicopathological features of graft versus host disease-associated myositis.Annals of clinical and translational neurology · 2024
    Review
  10. TCF-1 Is Required for CD4 T Cell Persistence Functions during AlloImmunity.International journal of molecular sciences · 2023
    Article
  11. Article
  12. Article
  13. Observational
  14. Review
  15. Article
  16. Review
  17. 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

2 authors at 1 institution in 1 country.

Hui WangColumbia Center for Translational Immunology, Columbia University College of Physicians and Surgeons, New York, NY, USA.
Yong-Guang Yang
Columbia University · US

Funding

XENOGRAFT TOLERANCE THROUGH MIXED CHIMERISMP01AI045897 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Megan Sykes · 2000 to 2026
$71.9M
STATISTICAL COREP01CA111519 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI PREFFER, FREDERIC IRA · 2006 to 2010
$9.3M
Role of CD47 in xenograft rejection by macrophagesR01AI064569 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI YANG, YONG-GUANG · 2008 to 2016
$3.1M
Immune response to allogeneic hESC-derived endothelial cells RC1HL100117 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI YANG, YONG-GUANG · 2010 to 2010
$895k
NCI NIH HHS P01 CA111519NCI NIH HHS P01CA111519NHLBI NIH HHS RC1 HL100117NIAID NIH HHS P01 AI045897NIAID NIH HHS P01AI045897NIAID NIH HHS R01 AI064569
6 · The paper itself

Abstract

Allogeneic hematopoietic cell transplantation (allo-HCT) is increasingly being performed to treat patients with hematologic malignancies. However, separating the beneficial graft-versus-tumor (GVT) or graft-versus-leukemia effects from graft-versus-host disease (GVHD) has been difficult and remains a significant challenge toward improving therapeutic efficacy and reducing toxicity of allo-HCT. GVHD is induced by donor T cells that also mediate potent anti-tumor responses. However, despite the largely shared effector mechanisms, extensive animal studies have demonstrated the potential of dissociating the GVT effect from GVHD. Also in many clinical cases, long-term remission was achieved following allo-HCT, without significant GVHD. A better mechanistic understanding of the immunopathophysiology of GVHD and GVT effects may potentially help to improve allo-HCT as well as maximize the benefit of GVT effects while minimizing GVHD. In this article, we review the role of IFN-γ in regulation of alloresponses following allo-HCT, with a focus on the mechanisms of how this cytokine may separate GVHD from GVT effects.

Indexed as

Hematopoietic Stem Cell TransplantationAnimalsGraft vs Host DiseaseGraft vs Tumor EffectHematologic NeoplasmsHumansInterferon-gammaSignal TransductionT-LymphocytesTreatment OutcomeIFNG protein, humanInterferon-gammaallogeneic hematopoietic cell transplantationDLIGVHDGVTIFN-γleukemia

Identifiers

PMID24517424
PMCPMC4040394
OpenAlexW2160431507

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.