Evidence map›Paper›PMID 22403259›Full record

ReviewBlood2012

Dendritic cells and regulation of graft-versus-host disease and graft-versus-leukemia activity.

Elizabeth O Stenger, Hēth R Turnquist, Markus Y Mapara, Angus W Thomson

Open access · bronzeAbstract readReview
In one paragraph

Review in Blood, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 3% 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

61 citing papers in PubMed, 1 synthesis or guideline pooled it, 107 citations in OpenAlex.

  1. Pooled it
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1 more citing papers are in PubMed but not listed here.

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 3 institutions in 1 country.

Elizabeth O StengerStarzl Transplantation Institute, Departments of Surgery and Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA 15261, USA.
Hēth R Turnquist
Markus Y Mapara
Angus W Thomson
University of Pittsburgh · USUniversity of Pittsburgh Medical Center · USUPMC Hillman Cancer Center · US

Funding

UNIVERSITY OF PITTSBURGH CLINICAL AND TRANSLATIONAL SCIENCE INSTITUTE: BPCAUL1RR024153 · NCRR · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2006 to 2011
$73.9M
University of Pittsburgh Clinical and Translational Science InstituteUL1TR000005 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$50.8M
Dermal-Epidermal Communication during Wound HealingR01GM063569 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WELLS, ALAN · 2003 to 2018
$3.7M
Role of STAT1 and STAT3 in Graft versus Host Disease and Graft versus Leukemia EfR01HL093716 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MAPARA, MARKUS Y · 2008 to 2012
$1.9M
Dendritic Cells, Rapamycin and Transplant ToleranceR01AI067541 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI THOMSON, ANGUS W · 2007 to 2010
$1.7M
Plasmacytoid Dendritic Cells and Transplant ToleranceR01AI060994 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI THOMSON, ANGUS W · 2005 to 2008
$1.1M
Influence of ST2 and IL-33 on cardiac allograft vasculopathy and outcomeR00HL097155 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI TURNQUIST, HETH R · 2011 to 2013
$723k
Influence of ST2 and IL-33 on cardiac allograft vasculopathy and outcomeK99HL097155 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI TURNQUIST, HETH R · 2009 to 2010
$174k
NCATS NIH HHS UL1 TR000005NCRR NIH HHS UL1 RR024153NHLBI NIH HHS K99 HL097155NHLBI NIH HHS K99/R00 HL97155NHLBI NIH HHS R00 HL097155NHLBI NIH HHS R01 HL093716NHLBI NIH HHS R01HL93716NIAID NIH HHS R01 AI060994NIAID NIH HHS R01 AI067541NIAID NIH HHS R01AI60994NIAID NIH HHS R01AI67541NIGMS NIH HHS R01 GM063569NIGMS NIH HHS R01GM63569
6 · The paper itself

Abstract

Hematopoietic stem cell transplantation is the only curative treatment for many malignant hematologic diseases, with an often critical graft-versus-leukemia effect. Despite peritransplant prophylaxis, GVHD remains a significant cause of posthematopoietic stem cell transplantation morbidity and mortality. Traditional therapies have targeted T cells, yet immunostimulatory dendritic cells (DCs) are critical in the pathogenesis of GVHD. Furthermore, DCs also have tolerogenic properties. Monitoring of DC characteristics may be predictive of outcome, and therapies that target DCs are innovative and promising. DCs may be targeted in vivo or tolerogenic (tol) DCs may be generated in vitro and given in the peritransplant period. Other cellular therapies, notably regulatory T cells (T(reg)) and mesenchymal stem cells, mediate important effects through DCs and show promise for the prevention and treatment of GVHD in early human studies. Therapies are likely to be more effective if they have synergistic effects or target both DCs and T cells in vivo, such as tolDCs or T(reg). Given the effectiveness of tolDCs in experimental models of GVHD and their safety in early human studies for type 1 diabetes, it is crucial that tolDCs be investigated in the prevention and treatment of human GVHD while ensuring conservation of graft-versus-leukemia effects.

Indexed as

Hematopoietic Stem Cell TransplantationImmune ToleranceAnimalsDendritic CellsDiabetes Mellitus, Type 1Graft vs Host DiseaseGraft vs Leukemia EffectHematologic NeoplasmsHumansT-Lymphocytes, RegulatoryTransplantation, Homologous

Identifiers

PMID22403259
PMCPMC3369606
OpenAlexW2061568638

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.