Evidence map›Paper›PMID 20445553›Full record

ArticleThe Journal of investigative dermatology2010

PD-1 on immature and PD-1 ligands on migratory human Langerhans cells regulate antigen-presenting cell activity.

Victor Peña-Cruz, Sean M McDonough, Felipe Diaz-Griffero, Christopher P Crum, Ruben D Carrasco, Gordon J Freeman

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 33 citations in OpenAlex.

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  14. Immunotherapies: the blockade of inhibitory signals.International journal of biological sciences · 2012
    Review
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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

6 authors at 3 institutions in 1 country.

Victor Peña-CruzDepartment of Medical Oncology, Dana-Farber Cancer Institute and Department of Medicine, Harvard Medical School, Boston, Massachusetts 02115, USA.
Sean M McDonough
Felipe Diaz-Griffero
Christopher P Crum
Ruben D Carrasco
Gordon J Freeman
Harvard University · USAlbert Einstein College of Medicine · USBrigham and Women's Hospital · US

Funding

Transgenic/KnockoutP01AI056299 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI SHARPE, ARLENE H. · 2003 to 2023
$42.5M
Targeting the PD-1 signaling pathway to rescue HIV T cell dysfunctionP01AI080192 · NIAID · EMORY UNIVERSITY · PI AHMED, RAFI · 2008 to 2012
$12.6M
Role of Cellular Factors in Retroviral Uncoating and Synthesis of Viral DNAR01AI087390 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI DIAZ-GRIFFERO, FELIPE · 2010 to 2024
$6.8M
Role of the B-box-v-1 Restriction by TRIM5alpha proteinsR00MH086162 · NIMH · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI DIAZ-GRIFFERO, FELIPE · 2010 to 2011
$496k
Role of the B-box-2 Domain in HIV-1 Restriction by TRIM5alpha proteinsK99MH086162 · NIMH · DANA-FARBER CANCER INST · PI DIAZ-GRIFFERO, FELIPE · 2009 to 2009
$89k
NIAID NIH HHS HHSN266200500030CNIAID NIH HHS P01 AI056299NIAID NIH HHS P01 AI080192NIAID NIH HHS R01 AI087390NIMH NIH HHS K99 MH086162NIMH NIH HHS R00 MH086162PHS HHS A1056299PHS HHS A108080192PHS HHS BAA-05-11
6 · The paper itself

Abstract

Langerhans cells (LCs) are known as "sentinels" of the immune system that function as professional antigen-presenting cells (APCs) after migration to draining lymph node. LCs are proposed to have a role in tolerance and the resolution of cutaneous immune responses. The Programmed Death-1 (PD-1) receptor and its ligands, PD-L1 and PD-L2, are a co-inhibitory pathway that contributes to the negative regulation of T-lymphocyte activation and peripheral tolerance. Surprisingly, we found PD-1 to be expressed on immature LCs (iLCs) in situ. PD-1 engagement on iLCs reduced IL-6 and macrophage inflammatory protein (MIP)-1alpha cytokine production in response to TLR2 signals but had no effect on LC maturation. PD-L1 and PD-L2 were expressed at very low levels on iLCs. Maturation of LCs upon migration from epidermis led to loss of PD-l expression and gain of high expression of PD-L1 and PD-L2 as well as co-stimulatory molecules. Blockade of PD-L1 and/or PD-L2 on migratory LCs (mLCs) and DDCs enhanced T-cell activation, as has been reported for other APCs. Thus the PD-1 pathway is active in iLCs and inhibits iLC activities, but expression of receptor and ligands reverses upon maturation and PD-L1 and PD-L2 on mLC function to inhibit T-cell responses.

Indexed as

Antigen PresentationAntigens, CDApoptosis Regulatory ProteinsB7-1 AntigenB7-2 AntigenB7-H1 AntigenCD83 AntigenCell CommunicationCell DifferentiationCell MovementCytokinesHumansImmunoglobulinsImmunophenotypingIntercellular Signaling Peptides and ProteinsJurkat CellsAntigens, CDApoptosis Regulatory ProteinsB7-1 AntigenB7-2 AntigenB7-H1 AntigenCD274 protein, humanCD83 AntigenCD86 protein, humanCytokinesImmunoglobulinsIntercellular Signaling Peptides and ProteinsLigandsMembrane GlycoproteinsPDCD1LG2 protein, humanPDCD1 protein, humanProgrammed Cell Death 1 Ligand 2 ProteinProgrammed Cell Death 1 ReceptorTLR2 protein, humanToll-Like Receptor 2

Identifiers

PMID20445553
PMCPMC2927196
OpenAlexW2037634641

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.