Evidence map›Paper›PMID 27077111›Full record

ArticleEBioMedicine2016

Functional Specialty of CD40 and Dendritic Cell Surface Lectins for Exogenous Antigen Presentation to CD8(+) and CD4(+) T Cells.

Wenjie Yin, Laurent Gorvel, Sandra Zurawski, Dapeng Li, Ling Ni, Dorothée Duluc, Katherine Upchurch, JongRok Kim, Chao Gu, Richard Ouedraogo and 6 more

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
3.4field-weighted citation impact, top 8% 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

38 citing papers in PubMed, 64 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 3 institutions in 2 countries.

Wenjie YinBaylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA; Institute of Biomedical Studies, Baylor University, South 5th Street, Waco, TX 76706, USA.
Laurent GorvelUnité de Recherche sur les Maladies Infectieuses, Tropicales Emergentes, IRD 198, CNRS UMR7278, INSERM U1095, 27 bd Jean Moulin, 13385 Cedex 05, Marseille, France.
Sandra ZurawskiBaylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA.
Dapeng LiBaylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA.
Ling NiBaylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA.
Dorothée DulucBaylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA.
Katherine UpchurchBaylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA; Institute of Biomedical Studies, Baylor University, South 5th Street, Waco, TX 76706, USA.
JongRok KimBaylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA.
Chao GuBaylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA; Institute of Biomedical Studies, Baylor University, South 5th Street, Waco, TX 76706, USA.
Richard OuedraogoBaylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA.
Zhiqing WangBaylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA.
Yaming XueBaylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA.
HyeMee JooBaylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA; Institute of Biomedical Studies, Baylor University, South 5th Street, Waco, TX 76706, USA.
Jean-Pierre GorvelCIML, Aix Marseille Université, CNRS UMR 7280, INSERM U1104, parc scientifique de Luminy, Case 906, Marseille, France.
Gerard ZurawskiBaylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA; Institute of Biomedical Studies, Baylor University, South 5th Street, Waco, TX 76706, USA.
SangKon OhBaylor Institute for Immunology Research, 3434 Live Oak Street, Dallas, TX 75204, USA; Institute of Biomedical Studies, Baylor University, South 5th Street, Waco, TX 76706, USA.
Baylor University · USInserm · FRInstitut de Recherche pour le Développement · FR

Funding

Targeting Dendritic Cells for Enhanced Musocal ImmunityU19AI057234 · NIAID · BAYLOR RESEARCH INSTITUTE · PI LEGRAND, ROGER · 2003 to 2013
$49.2M
NIAID NIH HHS U19 AI057234
6 · The paper itself

Abstract

Dendritic cells (DCs) are major antigen-presenting cells that can efficiently prime and cross-prime antigen-specific T cells. Delivering antigen to DCs via surface receptors is thus an appealing strategy to evoke cellular immunity. Nonetheless, which DC surface receptor to target to yield the optimal CD8(+) and CD4(+) T cell responses remains elusive. Herein, we report the superiority of CD40 over 9 different lectins and scavenger receptors at evoking antigen-specific CD8(+) T cell responses. However, lectins (e.g., LOX-1 and Dectin-1) were more efficient than CD40 at eliciting CD4(+) T cell responses. Common and distinct patterns of subcellular and intracellular localization of receptor-bound αCD40, αLOX-1 and αDectin-1 further support their functional specialization at enhancing antigen presentation to either CD8(+) or CD4(+) T cells. Lastly, we demonstrate that antigen targeting to CD40 can evoke potent antigen-specific CD8(+) T cell responses in human CD40 transgenic mice. This study provides fundamental information for the rational design of vaccines against cancers and viral infections.

Indexed as

Immunotherapy, ActiveAnimalsAntigen PresentationCD40 LigandCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCell DifferentiationDectin-1Dendritic CellsHumansLectinsLectins, C-TypeLymphocyte ActivationMiceMice, TransgenicRecombinant Fusion ProteinsCD40 LigandDectin-1LectinsLectins, C-TypeOlr1 protein, mouseRecombinant Fusion ProteinsScavenger Receptors, Class EANOVA, analysis of varianceAP, alkaline phosphataseAPC, antigen-presenting cellsCD40CD, cluster of differentiationCFSE, carboxyfluorescein succinimidyl esterCoh, cohesinCross-presentationCTL, cytotoxic T lymphocyteDC, dendritic cellDendritic cellDoc, dockerinEEA1, early endosome antigen 1ELISA, enzyme-linked immunosorbent assayELISpot, enzyme-linked immunospotFlu.M1, influenza virus matrix protein 1GM-CSF, granulocyte-macrophage colony-stimulating factorHA1, hemagglutinin subunit 1hCD40Tg, human CD40 transgenicHLA, human leukocyte antigenHPV, human papillomavirusHRP, horseradish peroxidaseIFN, interferonIL, interleukini.p., intraperitoneal(ly)JaCoP, Just another Colocalization PluginLAMP-1, lysosomal-associated membrane protein 1LectinsmAb, monoclonal antibodyMART-1, melanoma antigen recognized by T cells 1mDC, myeloid dendritic cellMHC, major histocompatibility complexMo-DC, monocyte-derived dendritic cellNHP, non-human primateNP, nucleoproteinPBMC, peripheral blood mononuclear cellsPBS, phosphate-buffered salinepDC, plasmacytoid dendritic cellPoly(I:C), polyinosinic:polycytidylic acidPSA, prostate specific antigens.c., subcutaneous(ly)TLR, toll-like receptorTMB, 3,3′,5,5′-tetramethylbenzidineTNF, tumor necrosis factorVaccine

Identifiers

PMID27077111
PMCPMC4816850
OpenAlexW2254172772

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.