Evidence map›Paper›PMID 22422880›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2012

Profound depletion of host conventional dendritic cells, plasmacytoid dendritic cells, and B cells does not prevent graft-versus-host disease induction.

Hongmei Li, Anthony J Demetris, Jennifer McNiff, Catherine Matte-Martone, Hung Sheng Tan, David M Rothstein, Fadi G Lakkis, Warren D Shlomchik

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.6field-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

46 citing papers in PubMed, 74 citations in OpenAlex.

  1. Review
  2. Article
  3. Alloreactive memory CD4 T cells promote transplant rejection by engaging DCs to induce innate inflammation and CD8 T cell priming.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Article
  11. The Pathophysiology and Treatment of Graft-Frontiers in immunology · 2021
    Review
  12. Article
  13. Review
  14. Plasmacytoid dendritic cells in the eye.Progress in retinal and eye research · 2021
    Review
  15. Article
  16. Review
  17. Review
  18. Article
  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

8 authors at 3 institutions in 1 country.

Hongmei LiCancer Center, Yale University School of Medicine, New Haven, CT 06520, USA.
Anthony J Demetris
Jennifer McNiff
Catherine Matte-Martone
Hung Sheng Tan
David M Rothstein
Fadi G Lakkis
Warren D Shlomchik
University of Pittsburgh · USYale University · USYale Cancer Center · US

Funding

Tolerance Through Induction of Regulatory T CellsP01AI064343 · NIAID · YALE UNIVERSITY · PI SHLOMCHIK, WARREN D · 2006 to 2010
$7.0M
Role of Tissue Antigen Presenting Cells in GVHDR01HL083072 · NHLBI · YALE UNIVERSITY · PI SHLOMCHIK, WARREN D · 2006 to 2015
$2.9M
NHLBI NIH HHS HL083072NHLBI NIH HHS R01 HL083072NIAID NIH HHS AI064343NIAID NIH HHS P01 AI064343
6 · The paper itself

Abstract

The efficacy of allogeneic hematopoietic stem cell transplantation is limited by graft-versus-host disease (GVHD). Host hematopoietic APCs are important initiators of GVHD, making them logical targets for GVHD prevention. Conventional dendritic cells (DCs) are key APCs for T cell responses in other models of T cell immunity, and they are sufficient for GVHD induction. However, we report in this article that in two polyclonal GVHD models in which host hematopoietic APCs are essential, GVHD was not decreased when recipient conventional DCs were inducibly or constitutively deleted. Additional profound depletion of plasmacytoid DCs and B cells, with or without partial depletion of CD11b(+) cells, also did not ameliorate GVHD. These data indicate that, in contrast with pathogen models, there is a surprising redundancy as to which host cells can initiate GVHD. Alternatively, very low numbers of targeted APCs were sufficient. We hypothesize the difference in APC requirements in pathogen and GVHD models relates to the availability of target Ags. In antipathogen responses, specialized APCs are uniquely equipped to acquire and present exogenous Ags, whereas in GVHD, all host cells directly present alloantigens. These studies make it unlikely that reagent-based host APC depletion will prevent GVHD in the clinic.

Indexed as

Hematopoietic Stem Cell TransplantationAnimalsB-LymphocytesCD11b AntigenCD8-Positive T-LymphocytesCytokinesDendritic CellsDiphtheria ToxinFemaleGraft vs Host DiseaseHumansIsoantigensLymphocyte DepletionMaleMiceMice, Inbred C57BLCD11b AntigenCytokinesDiphtheria ToxinIsoantigens

Identifiers

PMID22422880
PMCPMC3324629
OpenAlexW2096671282

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.