Evidence map›Paper›PMID 21768295›Full record

ArticleBlood2011

A repertoire-independent and cell-intrinsic defect in murine GVHD induction by effector memory T cells.

Kathryn W Juchem, Britt E Anderson, Cuiling Zhang, Jennifer M McNiff, Anthony J Demetris, Donna L Farber, Andrew J Caton, Warren D Shlomchik, Mark J Shlomchik

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

23 citing papers in PubMed, 40 citations in OpenAlex.

  1. Naive T-Cell Depletion to Prevent Chronic Graft-Versus-Host Disease.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2022
    Trial
  2. Trial
  3. Graft-Versus-Host Disease Mouse Models: A Clinical-Translational Perspective.Methods in molecular biology (Clifton, N.J.) · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Donor Allospecific CD44Frontiers in immunology · 2019
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Minor antigen distribution predicts site-specific graft-versus-tumor activity of adoptively transferred, minor antigen-specific CD8 T Cells.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2014
    Article
  18. Antigen and lymphopenia-driven donor T cells are differentially diminished by post-transplantation administration of cyclophosphamide after hematopoietic cell transplantation.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2013
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Kathryn W JuchemDepartment of Laboratory Medicine, Yale University School of Medicine, New Haven, CT 06520-8035, USA.
Britt E Anderson
Cuiling Zhang
Jennifer M McNiff
Anthony J Demetris
Donna L Farber
Andrew J Caton
Warren D Shlomchik
Mark J Shlomchik
Yale University · USThe Wistar Institute · USUniversity of Maryland, Baltimore · USUniversity of Pittsburgh · US

Funding

IMMUNOHEMATOLOGY/TRANSFUSION MEDICINE RESEARCH TRAININGT32HL007974 · NHLBI · YALE UNIVERSITY · PI JEANNE E HENDRICKSON, Diane S Krause · 2001 to 2026
$8.1M
Tolerance Through Induction of Regulatory T CellsP01AI064343 · NIAID · YALE UNIVERSITY · PI SHLOMCHIK, WARREN D · 2006 to 2010
$7.0M
RECEPTOR DIVERSITY IN RECOGNITION OF INFLUENZA HAR01AI024541 · NIAID · WISTAR INSTITUTE · PI CATON, ANDREW J · 1987 to 2012
$4.6M
MECHANISMS OF CHRONIC GVHD INITIATION AND PATHOGENESISR01HL066279 · NHLBI · YALE UNIVERSITY · PI SHLOMCHIK, MARK J · 2001 to 2009
$3.4M
Transfusion of Donor Effector Memory T Cells for GVL and Immune ReconstitutionR01HL109599 · NHLBI · YALE UNIVERSITY · PI SHLOMCHIK, MARK J, SHLOMCHIK, WARREN D · 2011 to 2015
$2.0M
NHLBI NIH HHS R01 HL066279NHLBI NIH HHS R01-HL066279NHLBI NIH HHS R01 HL109599NHLBI NIH HHS T32 HL007974NHLBI NIH HHS T32-HL007974NIAID NIH HHS P01 AI064343NIAID NIH HHS P01-AI064343NIAID NIH HHS R01 AI024541NIAID NIH HHS R01-AI24541
6 · The paper itself

Abstract

Effector memory T cells (T(EM)) do not cause graft-versus-host disease (GVHD), though why this is has not been elucidated. To compare the fates of alloreactive naive (T(N)) or memory (T(M)) T cells, we developed a model of GVHD in which donor T cells express a transgene-encoded TCR specific for an antigenic peptide that is ubiquitously expressed in the recipient. Small numbers of naive TCR transgenic (Tg) T cells induced a robust syndrome of GVHD in transplanted recipients. We then used an established method to convert TCR Tg cells to T(M) and tested these for GVHD induction. This allowed us to control for the potentially different frequencies of alloreactive T cells among T(N) and T(M), and to track fates of alloreactive T cells after transplantation. T(EM) caused minimal, transient GVHD whereas central memory T cells (T(CM)) caused potent GVHD. Surprisingly, T(EM) were not inert: they, engrafted, homed to target tissues, and proliferated extensively, but they produced less IFN-γ and their expansion in target tissues was limited at later time points, and local proliferation was reduced. Thus, cell-intrinsic properties independent of repertoire explain the impairment of T(EM), which can initiate but cannot sustain expansion and tissue damage.

Indexed as

AnimalsDisease Models, AnimalDNA-Binding ProteinsGraft vs Host DiseaseImmunologic MemoryMiceMice, Inbred BALB CMice, TransgenicPhenotypeStem Cell TransplantationT-LymphocytesTransplantation, HomologousDNA-Binding ProteinsRag2 protein, mouse

Identifiers

PMID21768295
PMCPMC3234673
OpenAlexW2027448345

What OpenQuestion holds

Textmetadata
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.