Evidence map›Paper›PMID 26065426›Full record

ArticlePloS one2015

B7-H3 Promotes Pathogenesis of Autoimmune Disease and Inflammation by Regulating the Activity of Different T Cell Subsets.

Liqun Luo, Gefeng Zhu, Haiying Xu, Sheng Yao, Gang Zhou, Yuwen Zhu, Koji Tamada, Lanqing Huang, Andrew D Flies, Megan Broadwater and 5 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. 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
5.1field-weighted citation impact, top 4% 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, 118 citations in OpenAlex.

  1. Article
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  9. Targeting glycolytic pathway in fibroblast-like synoviocytes for rheumatoid arthritis therapy: challenges and opportunities.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Review
  10. Article
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  13. Inhibition of the B7-H3 immune checkpoint limits hepatocellular carcinoma progression by enhancing T lymphocyte-mediated immune cytotoxicity in vitro and in vivo.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Article
  14. Article
  15. B7-H3 in Brain Malignancies: Immunology and Immunotherapy.International journal of biological sciences · 2023
    Review
  16. Article
  17. 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

15 authors at 6 institutions in 3 countries.

Liqun LuoInstitute of Immunotherapy, Sun Yat-Sen University, Guangzhou, Guangdong, China.
Gefeng ZhuDepartment of Immunobiology and Medicine, Yale University School of Medicine, New Haven, Connecticut, United States of America.
Haiying XuDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Sheng YaoDepartment of Immunobiology and Medicine, Yale University School of Medicine, New Haven, Connecticut, United States of America.
Gang ZhouDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Yuwen ZhuDepartment of Immunobiology and Medicine, Yale University School of Medicine, New Haven, Connecticut, United States of America.
Koji TamadaDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Lanqing HuangDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Andrew D FliesDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Megan BroadwaterDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
William RuffDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States of America.
Jan M A van DeursenDepartment of Pediatrics, Mayo Clinic, Rochester, Minnesota, United States of America.
Ignacio MeleroDepartment of Medicine, University of Navarra, Pamplona, Spain.
Zhou ZhuDepartment of Medicine, Yale University School of Medicine, New Haven, Connecticut, United States of America.
Lieping ChenDepartment of Immunobiology and Medicine, Yale University School of Medicine, New Haven, Connecticut, United States of America.
Yale University · USJohns Hopkins University · USJohns Hopkins Medicine · USMayo Clinic · USSun Yat-sen University · CNUniversidad de Navarra · ES

Funding

Treating lung inflammation by targeting SiglecsP01HL107151 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI SCHNAAR, RONALD L · 2011 to 2017
$15.4M
Therapeutic Manipulation of the B7-like MoleculesR01CA098731 · NCI · MAYO CLINIC COLL OF MEDICINE, ROCHESTER · PI CHEN, LIEPING · 2003 to 2007
$1.7M
Reversing tumor-specific CD4+ T-cell tolerance to control relapse after chemotherR01CA158202 · NCI · AUGUSTA UNIVERSITY · PI ZHOU, GANG · 2012 to 2016
$1.4M
NCI NIH HHS CA98731NCI NIH HHS R01 CA098731NCI NIH HHS R01 CA158202NHLBI NIH HHS HL107151NHLBI NIH HHS P01 HL107151
6 · The paper itself

Abstract

B7-H3 is a cell surface molecule in the immunoglobulin superfamily that is frequently upregulated in response to autoantigens and pathogens during host T cell immune responses. However, B7-H3's role in the differential regulation of T cell subsets remains largely unknown. Therefore, we constructed a new B7-H3 deficient mouse strain (B7-H3 KO) and evaluated the functions of B7-H3 in the regulation of Th1, Th2, and Th17 subsets in experimental autoimmune encephalomyelitis (EAE), experimental asthma, and collagen-induced arthritis (CIA); these mouse models were used to predict human immune responses in multiple sclerosis, asthma, and rheumatoid arthritis, respectively. Here, we demonstrate that B7-H3 KO mice have significantly less inflammation, decreased pathogenesis, and limited disease progression in both EAE and CIA mouse models when compared with littermates; these results were accompanied by a decrease in IFN-γ and IL-17 production. In sharp contrast, B7-H3 KO mice developed severe ovalbumin (OVA)-induced asthma with characteristic infiltrations of eosinophils in the lung, increased IL-5 and IL-13 in lavage fluid, and elevated IgE anti-OVA antibodies in the blood. Our results suggest B7-H3 has a costimulatory function on Th1/Th17 but a coinhibitory function on Th2 responses. Our studies reveal that B7-H3 could affect different T cell subsets which have important implications for regulating pathogenesis and disease progression in human autoimmune disease.

Indexed as

AnimalsApoptosisArthritis, ExperimentalAsthmaB7 AntigensBlotting, WesternCell DifferentiationCell ProliferationCells, CulturedEncephalomyelitis, Autoimmune, ExperimentalFemaleHumansImmunoenzyme TechniquesInflammationLymphocyte ActivationMiceB7 AntigensCd276 protein, mouseRNA, Messenger

Identifiers

PMID26065426
PMCPMC4465912
OpenAlexW1771275252

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Registered trials

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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.