Evidence map›Paper›PMID 23112154›Full record

Trial reportProceedings of the National Academy of Sciences of the United States of America2012

Immunoglobulin-like transcript receptors on human dermal CD14+ dendritic cells act as a CD8-antagonist to control cytotoxic T cell priming.

Jacques Banchereau, Sandra Zurawski, LuAnn Thompson-Snipes, Jean-Philippe Blanck, Sandra Clayton, Adiel Munk, Yanying Cao, Zhiqing Wang, Sunaina Khandelwal, Jiancheng Hu and 8 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

29 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
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  4. Emerging phagocytosis checkpoints in cancer immunotherapy.Signal transduction and targeted therapy · 2023
    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

18 authors at 3 institutions in 2 countries.

Jacques BanchereauBaylor Institute for Immunology Research and Baylor Research Institute, Dallas, TX 75204, USA.
Sandra Zurawski
LuAnn Thompson-Snipes
Jean-Philippe Blanck
Sandra Clayton
Adiel Munk
Yanying Cao
Zhiqing Wang
Sunaina Khandelwal
Jiancheng Hu
William H McCoy
Karolina A Palucka
Yoram Reiter
Daved H Fremont
Gerard Zurawski
Marco Colonna
Andrey S Shaw
Eynav Klechevsky
Baylor University · USWashington University in St. Louis · USTechnion – Israel Institute of Technology · IL

Funding

Targeting Dendritic Cells for Enhanced Musocal ImmunityU19AI057234 · NIAID · BAYLOR RESEARCH INSTITUTE · PI ZURAWSKI, GERARD · 2003 to 2013
$49.2M
Induction of melanoma immunity by dendritic cell subsetsP01CA084512 · NCI · ROCKEFELLER UNIVERSITY · PI BANCHEREAU, JACQUES F · 2000 to 2010
$12.1M
Structure and Function of the Immunological SynapseR37AI057966 · NIAID · WASHINGTON UNIVERSITY · PI SHAW, ANDREY S. · 2004 to 2013
$3.2M
SUBPOPULATIONS OF HUMAN DENDRITIC CELLSR01CA078846 · NCI · BAYLOR RESEARCH INSTITUTE · PI BANCHEREAU, JACQUES F · 1999 to 2008
$2.5M
HLA-G - LILRB - SHP2 Axis in Airway Smooth MuscleR01HL097805 · NHLBI · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2009 to 2012
$2.1M
Dendritic Cells, Heat Shock Proteins and Tumor ImmunityR01CA085540 · NCI · BAYLOR RESEARCH INSTITUTE · PI BANCHEREAU, JACQUES F · 2001 to 2004
$1.0M
NCI NIH HHS P01 CA084512NCI NIH HHS P0-1 CA84512NCI NIH HHS R01 CA078846NCI NIH HHS R01 CA085540NCI NIH HHS R0-1 CA78846NCI NIH HHS R0-1 CA85540NHLBI NIH HHS 5R01HL097805NHLBI NIH HHS R01 HL097805NIAID NIH HHS R37 AI057966NIAID NIH HHS U19 AI057234NIAID NIH HHS U-19 AI-57234
6 · The paper itself

Abstract

Human Langerhans cells (LCs) are highly efficient at priming cytolytic CD8(+) T cells compared with dermal CD14(+) dendritic cells (DCs). Here we show that dermal CD14(+) DCs instead prime a fraction of naïve CD8(+) T cells into cells sharing the properties of type 2 cytokine-secreting CD8(+) T cells (TC2). Differential expression of the CD8-antagonist receptors on dermal CD14(+) DCs, the Ig-like transcript (ILT) inhibitory receptors, explains the difference between the two types of DCs. Inhibition of CD8 function on LCs inhibited cytotoxic T lymphocytes (CTLs) and enhanced TC2 generation. In addition, blocking ILT2 or ILT4 on dermal CD14(+) DCs enhanced the generation of CTLs and inhibited TC2 cytokine production. Lastly, addition of soluble ILT2 and ILT4 receptors inhibited CTL priming by LCs. Thus, ILT receptor expression explains the polarization of CD8(+) T-cell responses by LCs vs. dermal CD14(+) DCs.

Indexed as

Lipopolysaccharide ReceptorsAntigens, CDDermisHumansLangerhans CellsLeukocyte Immunoglobulin-like Receptor B1Membrane GlycoproteinsReceptors, ImmunologicT-Lymphocytes, CytotoxicAntigens, CDLeukocyte Immunoglobulin-like Receptor B1LILRB1 protein, humanLILRB2 protein, humanLipopolysaccharide ReceptorsMembrane GlycoproteinsReceptors, Immunologic

Identifiers

PMID23112154
PMCPMC3503187
OpenAlexW2040761710

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.