Evidence map›Paper›PMID 20530286›Full record

ArticleBlood2010

Cross-priming CD8+ T cells by targeting antigens to human dendritic cells through DCIR.

Eynav Klechevsky, Anne-Laure Flamar, Yanying Cao, Jean-Philippe Blanck, Maochang Liu, Amy O'Bar, Olivier Agouna-Deciat, Peter Klucar, Luann Thompson-Snipes, Sandra Zurawski and 4 more

Open access · greenAbstract read
In one paragraph

Article in Blood, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 121 papers.

0numbers the graph read from it
0cells of the map it votes in
121citing papers in PubMed
8.9field-weighted citation impact, top 1% 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

121 citing papers in PubMed, 203 citations in OpenAlex.

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  14. The aryl hydrocarbon receptor instructs the immunomodulatory profile of a subset of Clec4a4Proceedings of the National Academy of Sciences of the United States of America · 2022
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61 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

14 authors at 3 institutions in 3 countries.

Eynav KlechevskyBaylor Institute for Immunology Research and Inserm U899, Dallas, TX 75204, USA.
Anne-Laure Flamar
Yanying Cao
Jean-Philippe Blanck
Maochang Liu
Amy O'Bar
Olivier Agouna-Deciat
Peter Klucar
Luann Thompson-Snipes
Sandra Zurawski
Yoram Reiter
A Karolina Palucka
Gerard Zurawski
Jacques Banchereau
Baylor University · USTechnion – Israel Institute of Technology · ILIcahn School of Medicine at Mount Sinai · US

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
SUBPOPULATIONS OF HUMAN DENDRITIC CELLSR01CA078846 · NCI · BAYLOR RESEARCH INSTITUTE · PI BANCHEREAU, JACQUES F · 1999 to 2008
$2.5M
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 CA85540NIAID NIH HHS U19 AI057234NIAID NIH HHS U-19 AI-57234
6 · The paper itself

Abstract

We evaluated human CD8(+) T-cell responses generated by targeting antigens to dendritic cells (DCs) through various lectin receptors. We found the immunoreceptor tyrosine-based inhibitory motif-containing DC immunoreceptor (DCIR) to mediate potent cross-presentation. A single exposure to a low dose of anti-DCIR-antigen conjugate initiated antigen-specific CD8(+) T-cell immunity by all human DC subsets including ex vivo-generated DCs, skin-isolated Langerhans cells, and blood myeloid DCs and plasmacytoid DCs. The delivery of influenza matrix protein (FluMP) through DCIR resulted in expansion of FluMP-specific memory CD8(+) T cells. Enhanced specific CD8(+) T-cell responses were observed when an antigen was delivered to the DCs via DCIR, compared with those induced by a free antigen, or antigen conjugated to a control monoclonal antibody or delivered via DC-SIGN, another lectin receptor. DCIR targeting also induced primary CD8(+) T-cell responses against self (MART-1) and viral (HIV gag) antigens. Addition of Toll-like receptor (TLR) 7/8 agonist enhanced DCIR-mediated cross-presentation as well as cross-priming, particularly when combined with a CD40 signal. TLR7/8 activation was associated with increased expansion of the primed CD8(+) T cells, high production of interferon-γ and tumor necrosis factor-α, and reduced levels of type 2-associated cytokines. Thus, antigen targeting via the human DCIR receptor allows activation of specific CD8(+) T-cell immunity.

Indexed as

AnimalsAntibodies, MonoclonalAntigensAntigens, NeoplasmB-LymphocytesCD8-Positive T-LymphocytesCells, CulturedCross-PrimingDendritic CellsFlow Cytometrygag Gene Products, Human Immunodeficiency VirusHumansLangerhans CellsLectins, C-TypeMART-1 AntigenMembrane GlycoproteinsAntibodies, MonoclonalAntigensAntigens, NeoplasmCL 075CLEC4A protein, humangag Gene Products, Human Immunodeficiency VirusLectins, C-TypeMART-1 AntigenMembrane GlycoproteinsMLANA protein, humanMlana protein, mouseNeoplasm ProteinsQuinolinesReceptors, ImmunologicThiazolesToll-Like Receptor 7Toll-Like Receptor 8

Identifiers

PMID20530286
PMCPMC2947393
OpenAlexW2084697718

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.