Evidence map›Paper›PMID 25902483›Full record

ArticleImmunity2015

A dendritic-cell-stromal axis maintains immune responses in lymph nodes.

Varsha Kumar, Dragos C Dasoveanu, Susan Chyou, Te-Chen Tzeng, Cristina Rozo, Yong Liang, William Stohl, Yang-Xin Fu, Nancy H Ruddle, Theresa T Lu

Open access · bronzeAbstract read
In one paragraph

Article in Immunity, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

55 citing papers in PubMed, 89 citations in OpenAlex.

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  11. CD47 promotes peripheral T cell survival by preventing dendritic cell-mediated T cell necroptosis.Proceedings of the National Academy of Sciences of the United States of America · 2023
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  14. CD169European journal of immunology · 2022
    Article
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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

10 authors at 4 institutions in 1 country.

Varsha KumarAutoimmunity and Inflammation Program, Hospital for Special Surgery, New York, NY 10021, USA.
Dragos C DasoveanuAutoimmunity and Inflammation Program, Hospital for Special Surgery, New York, NY 10021, USA.
Susan ChyouAutoimmunity and Inflammation Program, Hospital for Special Surgery, New York, NY 10021, USA.
Te-Chen TzengAutoimmunity and Inflammation Program, Hospital for Special Surgery, New York, NY 10021, USA.
Cristina RozoAutoimmunity and Inflammation Program, Hospital for Special Surgery, New York, NY 10021, USA.
Yong LiangDepartment of Pathology, Pritzker School of Medicine, University of Chicago, Chicago, IL 60637, USA.
William StohlDepartment of Rheumatology, Keck School of Medicine of USC, Los Angeles, CA 90033, USA.
Yang-Xin FuDepartment of Pathology, Pritzker School of Medicine, University of Chicago, Chicago, IL 60637, USA.
Nancy H RuddleDepartment of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT 06520, USA.
Theresa T LuAutoimmunity and Inflammation Program, Hospital for Special Surgery, New York, NY 10021, USA; Pediatric Rheumatology, Hospital for Special Surgery, New York, NY 10021, USA; Department of Microbiology and Immunology, Weill Cornell Medical College, New York, NY, 10021, USA. Electronic address: lut@hss.edu.
Hospital for Special Surgery · USUniversity of Chicago · USKeck Hospital of USC · USYale University · US

Funding

Vascular-stromal function and regulation in immunityR01AI079178 · NIAID · HOSPITAL FOR SPECIAL SURGERY · PI Theresa T. Lu · 2010 to 2026
$6.6M
Cell SorterS10OD019986 · OD · HOSPITAL FOR SPECIAL SURGERY · PI LU, THERESA T. · 2015 to 2015
$600k
NIAID NIH HHS R01 AI079178NIH HHS S10 OD019986
6 · The paper itself

Abstract

Within secondary lymphoid tissues, stromal reticular cells support lymphocyte function, and targeting reticular cells is a potential strategy for controlling pathogenic lymphocytes in disease. However, the mechanisms that regulate reticular cell function are not well understood. Here we found that during an immune response in lymph nodes, dendritic cells (DCs) maintain reticular cell survival in multiple compartments. DC-derived lymphotoxin beta receptor (LTβR) ligands were critical mediators, and LTβR signaling on reticular cells mediated cell survival by modulating podoplanin (PDPN). PDPN modulated integrin-mediated cell adhesion, which maintained cell survival. This DC-stromal axis maintained lymphocyte survival and the ongoing immune response. Our findings provide insight into the functions of DCs, LTβR, and PDPN and delineate a DC-stromal axis that can potentially be targeted in autoimmune or lymphoproliferative diseases.

Indexed as

AnimalsCell AdhesionCell SurvivalDendritic CellsGene Expression RegulationImmunophenotypingLymph NodesLymphocyte DepletionLymphotoxin beta ReceptorMembrane GlycoproteinsMiceMice, Inbred C57BLMice, TransgenicPodoplaninSignal TransductionStromal CellsLtbr protein, mouseLymphotoxin beta ReceptorMembrane GlycoproteinsPdpn protein, mousePodoplanin

Identifiers

PMID25902483
PMCPMC4591553
OpenAlexW2078050357

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.