Evidence map›Paper›PMID 31084709›Full record

ArticleeLife2019

IgE-mediated mast cell activation promotes inflammation and cartilage destruction in osteoarthritis.

Qian Wang, Christin M Lepus, Harini Raghu, Laurent L Reber, Mindy M Tsai, Heidi H Wong, Ericka von Kaeppler, Nithya Lingampalli, Michelle S Bloom, Nick Hu and 11 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
5.3field-weighted citation impact, top 3% 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

85 citing papers in PubMed, 130 citations in OpenAlex.

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  17. Biomedicines · 2025
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25 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

21 authors at 5 institutions in 3 countries.

Qian Wang *GRECC, VA Palo Alto Health Care System, Palo Alto, United States.
Christin M Lepus *GRECC, VA Palo Alto Health Care System, Palo Alto, United States.
Harini Raghu *GRECC, VA Palo Alto Health Care System, Palo Alto, United States.
Laurent L ReberDepartment of Pathology, Stanford University School of Medicine, Stanford, United States.
Mindy M TsaiDepartment of Pathology, Stanford University School of Medicine, Stanford, United States.
Heidi H WongGRECC, VA Palo Alto Health Care System, Palo Alto, United States.
Ericka von KaepplerGRECC, VA Palo Alto Health Care System, Palo Alto, United States.
Nithya LingampalliGRECC, VA Palo Alto Health Care System, Palo Alto, United States.
Michelle S BloomGRECC, VA Palo Alto Health Care System, Palo Alto, United States.
Nick HuGRECC, VA Palo Alto Health Care System, Palo Alto, United States.
Eileen E ElliottGRECC, VA Palo Alto Health Care System, Palo Alto, United States.
Francesca OlivieroRheumatology Unit, Department of Medicine, University of Padova, Padova, Italy.
Leonardo PunziRheumatology Unit, Department of Medicine, University of Padova, Padova, Italy.
Nicholas J GioriGRECC, VA Palo Alto Health Care System, Palo Alto, United States.
Stuart B GoodmanDepartment of Orthopedic Surgery, Stanford University School of Medicine, Stanford, United States.
Constance R ChuGRECC, VA Palo Alto Health Care System, Palo Alto, United States.
Jeremy SokoloveGRECC, VA Palo Alto Health Care System, Palo Alto, United States.
Yoshihiro FukuokaDepartment of Internal Medicine, Virginia Commonwealth University School of Medicine, Richmond, United States.
Lawrence B SchwartzDepartment of Internal Medicine, Virginia Commonwealth University School of Medicine, Richmond, United States.
Stephen J GalliDepartment of Pathology, Stanford University School of Medicine, Stanford, United States.
William H RobinsonGRECC, VA Palo Alto Health Care System, Palo Alto, United States.ORCID 0000-0003-4385-704X
VA Palo Alto Health Care System · USStanford University · USUniversity of Padua · ITVirginia Commonwealth University · USCentre National de la Recherche Scientifique · FR

Funding

Role of nociceptive sensory neuron/mast cell interactions in cutaneous allergic inflammationR01AI132494 · NIAID · STANFORD UNIVERSITY · PI GALLI, STEPHEN JOSEPH · 2017 to 2021
$2.4M
RabGEF1 in MyD88 signaling, skin immunity, and atopic dermatitisR01AR067145 · NIAMS · STANFORD UNIVERSITY · PI GALLI, STEPHEN JOSEPH · 2015 to 2019
$1.9M
Transmission Electron MicroscopeS10RR026780 · NCRR · STANFORD UNIVERSITY · PI TALBOT, WILLIAM S · 2010 to 2010
$412k
Investigating the Role of Fc Receptors in the Pathogenesis of OsteoarthritisI01BX002345 · VA · VETERANS ADMIN PALO ALTO HEALTH CARE SYS · PI ROBINSON, WILLIAM H · 2014 to 2017
–
Inflammatory Mechanisms in Traumatic Joint Injury and RepairI01RX000588 · VA · VETERANS ADMIN PALO ALTO HEALTH CARE SYS · PI ROBINSON, WILLIAM H · 2012 to 2015
–
The Role of Coagulation and Fibrinolysis in Post-Traumatic OsteoarthritisI01RX000934 · VA · VETERANS ADMIN PALO ALTO HEALTH CARE SYS · PI ROBINSON, WILLIAM H · 2015 to 2017
–
BLRD VA I01 BX002345NCRR NIH HHS 1S10RR026780-01NCRR NIH HHS S10 RR026780NIAID NIH HHS R01 AI132494NIAMS NIH HHS R01 AR067145NIH HHS R01AI132494NIH HHS R01AR067145RRD VA I01 RX000588RRD VA I01 RX000934RRD VA I01 RX002689U.S. Department of Veterans Affairs I01BX002345U.S. Department of Veterans Affairs I01RX000588U.S. Department of Veterans Affairs I01RX000934U.S. Department of Veterans Affairs I01RX002689
6 · The paper itself

Abstract

Osteoarthritis is characterized by articular cartilage breakdown, and emerging evidence suggests that dysregulated innate immunity is likely involved. Here, we performed proteomic, transcriptomic, and electron microscopic analyses to demonstrate that mast cells are aberrantly activated in human and murine osteoarthritic joint tissues. Using genetic models of mast cell deficiency, we demonstrate that lack of mast cells attenuates osteoarthritis in mice. Using genetic and pharmacologic approaches, we show that the IgE/FcεRI/Syk signaling axis is critical for the development of osteoarthritis. We find that mast cell-derived tryptase induces inflammation, chondrocyte apoptosis, and cartilage breakdown. Our findings demonstrate a central role for IgE-dependent mast cell activation in the pathogenesis of osteoarthritis, suggesting that targeting mast cells could provide therapeutic benefit in human osteoarthritis. Editorial note: This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed (see decision letter).

Indexed as

AnimalsCartilageGene Expression ProfilingHumansImmunoglobulin EImmunologic FactorsMast CellsMiceMicroscopy, ElectronOsteoarthritisProteomicsSignal TransductionImmunoglobulin EImmunologic Factorshumanimmunologyinflammationinnate immunitymast cellmouseosteoarthritis

Identifiers

PMID31084709
PMCPMC6516833
OpenAlexW2946058236

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.