Evidence map›Paper›PMID 22809867›Full record

ArticleBiology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation2012

Allospecific CD4(+) effector memory T cells do not induce graft-versus-host disease in mice.

Ping Zhang, Jieying Wu, Divino Deoliveira, Nelson J Chao, Benny J Chen

Open access · hybridAbstract read
In one paragraph

Article in Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

16 citing papers in PubMed, 23 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. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Donor Allospecific CD44Frontiers in immunology · 2019
    Article
  9. Article
  10. Article
  11. Alloimmune T cells in transplantation.The Journal of clinical investigation · 2017
    Review
  12. Article
  13. Article
  14. Article
  15. Antibody- and aptamer-strategies for GvHD prevention.Journal of cellular and molecular medicine · 2015
    Review
  16. 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

5 authors at 2 institutions in 2 countries.

Ping ZhangDepartment of Medicine, Duke University Medical Center, Durham, NC 27710, USA.
Jieying Wu
Divino Deoliveira
Nelson J Chao
Benny J Chen
Duke Medical Center · USDuke University Hospital · US

Funding

THERAPEUTIC APPROACHES TO OVARIAN/BREAST CANCER--HIGH DOSE CHEMOTHERAPY AND ABMSP01CA047741 · NCI · DUKE UNIVERSITY · PI HASSELBLAD, VICTOR · 1990 to 2013
$19.5M
Preclinical studies of unrelated cord blood transplantationP01HL067314 · NHLBI · DUKE UNIVERSITY · PI CHAO, NELSON J. · 2002 to 2005
$6.9M
NCI NIH HHS P01 CA047741NCI NIH HHS P01-CA47741NHLBI NIH HHS P01 HL067314NHLBI NIH HHS P01-HL67314
6 · The paper itself

Abstract

We studied whether allospecific CD4(+) effector memory T cells (T(EM)) could induce graft-versus-host disease (GVHD) using a novel GVHD model induced solely by CD4(+) T cell receptor transgenic TEa cells. Allospecific T(EM) generated in a lymphopenic host bore a typical memory phenotype. Moreover, these cells were able to elicit a faster and more effective proliferative response on challenge with alloantigen in vitro and to mediate "second-set" skin graft rejection in vivo. However, these allospecific T(EM) were unable to induce GVHD. Allospecific T(EM) recipients became tolerant to alloantigen as a result of clonal deletion. Even though allospecific T(EM) were able to respond to alloantigen initially, the expansion of these cells and inflammatory cytokine production during GVHD were dramatically decreased. The inability of allospecific T(EM) to sustain the alloresponse may be a result of enhanced activation-induced cell death. These observations provide insight into how allospecific CD4(+) T(EM) respond to alloantigen during GVHD and underscore the fundamental differences in alloresponses mediated by allospecific T(EM) in graft rejection and GVHD settings.

Indexed as

AnimalsCD4-Positive T-LymphocytesCell DeathClonal AnergyClonal DeletionCytokinesFemaleGraft vs Host DiseaseImmunologic MemoryIsoantigensMiceMice, Inbred C57BLMice, TransgenicReceptors, Antigen, T-CellSkin TransplantationT-Lymphocyte SubsetsCytokinesIsoantigensReceptors, Antigen, T-Cell

Identifiers

PMID22809867
PMCPMC3443280
OpenAlexW2097339082

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.