Evidence map›Paper›PMID 35254128›Full record

ArticlemBio2022

Interleukin-17 Contributes to Chikungunya Virus-Induced Disease.

Xiang Liu, Yee-Suan Poo, Juliana C Alves, Roque P Almeida, Helen Mostafavi, Patrick Chun Hean Tang, Richard Bucala, Mauro M Teixeira, Adam Taylor, Ali Zaid and 1 more

Open access · goldAbstract read
In one paragraph

Article in mBio, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
6.2field-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

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

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  19. Research progress of mosquito-borne virus mRNA vaccines.Molecular therapy. Methods & clinical development · 2025
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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

11 authors at 4 institutions in 3 countries.

Xiang LiuMenzies Health Institute Queensland, Griffith Universitygrid.1022.1, Southport, Queensland, Australia.ORCID 0000-0002-8165-3294
Yee-Suan PooMenzies Health Institute Queensland, Griffith Universitygrid.1022.1, Southport, Queensland, Australia.
Juliana C AlvesDivision of Immunology and Molecular Biology Laboratory, University Hospital/EBSERH, Federal University of Sergipe, Aracaju, Sergipe, Brazil.
Roque P AlmeidaDivision of Immunology and Molecular Biology Laboratory, University Hospital/EBSERH, Federal University of Sergipe, Aracaju, Sergipe, Brazil.
Helen MostafaviMenzies Health Institute Queensland, Griffith Universitygrid.1022.1, Southport, Queensland, Australia.
Patrick Chun Hean TangMenzies Health Institute Queensland, Griffith Universitygrid.1022.1, Southport, Queensland, Australia.
Richard BucalaDepartment of Internal Medicine, Yale Universitygrid.47100.32 School of Medicine, New Haven, Connecticut, USA.
Mauro M TeixeiraDepartment of Biochemistry and Immunology, Universidade Federal de Minas Geraisgrid.8430.f, Belo Horizonte, Brazil.
Adam TaylorMenzies Health Institute Queensland, Griffith Universitygrid.1022.1, Southport, Queensland, Australia.ORCID 0000-0002-7159-3961
Ali Zaid *Menzies Health Institute Queensland, Griffith Universitygrid.1022.1, Southport, Queensland, Australia.ORCID 0000-0002-2528-2783
Suresh Mahalingam *Menzies Health Institute Queensland, Griffith Universitygrid.1022.1, Southport, Queensland, Australia.ORCID 0000-0003-3141-8410
Griffith University · AUUniversidade Federal de Sergipe · BRUniversidade Federal de Minas Gerais · BRYale University · US

Funding

Defining the Pathogenic Contribution of High Genotypic MIF ExpressionR01AR078334 · NIAMS · YALE UNIVERSITY · PI BUCALA, RICHARD J · 2021 to 2025
$1.8M
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) 001Department of Health | National Health and Medical Research Council (NHMRC) 1079086MCTI | Financiadora de Estudos e Projetos (FINEP) 0116005600NIAMS NIH HHS R01 AR078334
6 · The paper itself

Abstract

Alphaviral arthritides caused by mosquito-borne arboviruses such as chikungunya virus (CHIKV) can persist for months after the initial acute disease. Here, we investigated the contribution of interleukin-17 (IL-17), a cytokine involved in chronic autoimmune arthropathies such as rheumatoid arthritis, to the development of alphaviral arthropathy. Sera from CHIKV-infected patients who displayed both acute and chronic disease showed high levels of IL-17, IL-6, IL-21, IL-22, and IL-23, especially during the chronic phase of disease. We sought to validate these findings using a mouse model of CHIKV infection and disease using wild-type and IL-17A-deficient mice. Mice were infected with CHIKV, and joint and muscle tissues were harvested at designated time points. Tissue infiltrates were examined by immunohistochemistry, and tissue mRNA and protein expression of cytokines was assessed. Joint and muscle pathology was assessed using histology. CHIKV-infected mice lacking IL-17A showed reduced tissue inflammation and neutrophil infiltration, compared to wild-type mice. These investigations showed a role for IL-17 in the acute phase of CHIKV infection and also during the postacute disease resolution phase.

Indexed as

Arthritis, RheumatoidChikungunya FeverChikungunya virusAnimalsCytokinesHumansInflammationInterleukin-17MiceCytokinesIL17A protein, humanIl17a protein, mouseInterleukin-17alphaviruschikungunyainterleukin-17

Identifiers

PMID35254128
PMCPMC9040832
OpenAlexW4220897686

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.