Evidence map›Paper›PMID 12823271›Full record

ReviewClinical and experimental immunology2003

Dendritic cells, T cell tolerance and therapy of adverse immune reactions.

P A Morel, M Feili-Hariri, P T Coates, A W Thomson

Open access · bronzeAbstract readReview
In one paragraph

Review in Clinical and experimental immunology, 2003. 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
3.2field-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

16 citing papers in PubMed, 76 citations in OpenAlex.

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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 1 institution in 1 country.

P A MorelDepartment of Immunology, University of Pittsburgh Medical Center, Pittsburgh, PA 15213, USA.
M Feili-Hariri
P T Coates
A W Thomson
University of Pittsburgh Medical Center · US

Funding

MECHANISMS OF DENDRITIC CELL BASED TUMOR IMMUNIZATIONP01CA073743 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FINN, OLIVERA J · 1998 to 2009
$12.3M
RHESUS MONKEY DENDRITIC CELLS FOR TRANSPLANT TOLERANCEU01AI051698 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI THOMSON, ANGUS W · 2002 to 2011
$4.9M
GENE ENGINEERING OF DENDRITIC CELLS AND TRANSPLANTATIONR01AI041011 · NIAID · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI THOMSON, ANGUS W · 1997 to 2006
$1.5M
LIVER TRANSPLANTATION: THE ROLE OF DENDRITIC CELLSR01DK049745 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI THOMSON, ANGUS W · 1996 to 2005
$1.4M
NCI NIH HHS CA73743NCI NIH HHS P01 CA073743NIAID NIH HHS AI41011NIAID NIH HHS AI/DK 51698NIAID NIH HHS R01 AI041011NIAID NIH HHS U01 AI051698NIDDK NIH HHS DK 49745NIDDK NIH HHS R01 DK049745
6 · The paper itself

Abstract

Dendritic cells (DC) are uniquely able to either induce immune responses or to maintain the state of self tolerance. Recent evidence has shown that the ability of DC to induce tolerance in the steady state is critical to the prevention of the autoimmune response. Likewise, DC have been shown to induce several type of regulatory T cells including Th2, Tr1, Ts and NKT cells, depending on the maturation state of the DC and the local microenvironment. DC have been shown to have therapeutic value in models of allograft rejection and autoimmunity, although no success has been reported in allergy. Several strategies, including the use of specific DC subsets, genetic modification of DC and the use of DC at various maturation stages for the treatment of allograft rejection and autoimmune disease are discussed. The challenge for the future use of DC therapy in human disease is to identify the appropriate DC for the proposed therapy; a task made more daunting by the extreme plasticity of DC that has recently been demonstrated. However, the progress achieved to date suggests that these are not insurmountable obstacles and that DC may become a useful therapeutic tool in transplantation and autoimmune disease.

Indexed as

AnimalsAsthmaAutoimmune DiseasesDendritic CellsGenetic EngineeringGraft RejectionHumansMiceOrgan TransplantationSelf ToleranceT-LymphocytesTransplantation, Homologous

Identifiers

PMID12823271
PMCPMC1808741
OpenAlexW2072872611

What OpenQuestion holds

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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.