Evidence map›Paper›PMID 38507338›Full record

ArticlePloS one2024

Cytokine and T cell responses in post-chikungunya viral arthritis: A cross-sectional study.

Aileen Y Chang, Sarah R Tritsch, Carlos Andres Herrera Gomez, Liliana Encinales, Andres Cadena Bonfanti, Wendy Rosales, Evelyn Mendoza-Torres, Samuel Simmens, Richard L Amdur, Christopher N Mores and 26 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

5 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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  4. Review
  5. Article
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

36 authors at 8 institutions in 2 countries.

Aileen Y ChangDepartment of Medicine, George Washington University, Washington, DC, United States of America.ORCID 0000-0001-7410-9867
Sarah R TritschDepartment of Global Health, Milken Institute School of Public Health, George Washington University, Washington, DC, United States of America.
Carlos Andres Herrera GomezDepartment of Medicine, George Washington University, Washington, DC, United States of America.
Liliana EncinalesDepartment of Medicine, Allied Research Society, Barranquilla, Atlántico, Colombia.
Andres Cadena BonfantiCentro de Investigación, Clínica de la Costa SAS, Barranquilla, Atlántico, Colombia.
Wendy RosalesAdvanced Biomedicine Research Group, Universidad Libre de Colombia, Seccional Barranquilla, Barranquilla, Atlántico, Colombia.
Evelyn Mendoza-TorresAdvanced Biomedicine Research Group, Universidad Libre de Colombia, Seccional Barranquilla, Barranquilla, Atlántico, Colombia.
Samuel SimmensDepartment of Biostatistics and Bioinformatics, Milken Institute School of Public Health, George Washington University, Washington, DC, United States of America.ORCID 0000-0001-7830-8003
Richard L AmdurFeinstein Institute for Medical Research, Northwell Health, Manhasset, New York, United States of America.
Christopher N MoresDepartment of Global Health, Milken Institute School of Public Health, George Washington University, Washington, DC, United States of America.
Paige FierbaughDepartment of Medicine, George Washington University, Washington, DC, United States of America.ORCID 0000-0002-3978-2279
Carlos Alberto Perez HernandezCentro de Investigación, Clínica de la Costa SAS, Barranquilla, Atlántico, Colombia.
Geraldine AvendañoCentro de Investigación, Clínica de la Costa SAS, Barranquilla, Atlántico, Colombia.
Paula Bruges SilveraCentro de Investigación, Clínica de la Costa SAS, Barranquilla, Atlántico, Colombia.
Yerlenis Galvis CrespoCentro de Investigación, Clínica de la Costa SAS, Barranquilla, Atlántico, Colombia.
Alberto David Cabana JimenezCentro de Investigación, Clínica de la Costa SAS, Barranquilla, Atlántico, Colombia.
Jennifer Carolina Martinez ZapataCentro de Investigación, Clínica de la Costa SAS, Barranquilla, Atlántico, Colombia.
Dennys JimenezCentro de Investigación, Clínica de la Costa SAS, Barranquilla, Atlántico, Colombia.
Estefanie Osorio-LlanesAdvanced Biomedicine Research Group, Universidad Libre de Colombia, Seccional Barranquilla, Barranquilla, Atlántico, Colombia.ORCID 0000-0002-8682-8874
Jairo Castellar-LopezAdvanced Biomedicine Research Group, Universidad Libre de Colombia, Seccional Barranquilla, Barranquilla, Atlántico, Colombia.
Karol SuchowieckiDepartment of Medicine, George Washington University, Washington, DC, United States of America.ORCID 0000-0002-7012-3028
Karen MartinsU.S. Army Medical Research Institute of Infectious Diseases, Frederick, Maryland, United States of America.
Melissa GregoryHenry M. Jackson Foundation, In Support of Austere Environments Consortium for Enhanced Sepsis Outcomes (ACESO), Bethesda, Maryland, United States of America.
Ivan ZuluagaUniversidad Libre de Barranquilla, Clínica Iberoamérica, Barranquilla, Atlántico, Colombia.
Abigale ProctorDepartment of Global Health, Milken Institute School of Public Health, George Washington University, Washington, DC, United States of America.
Alfonso Sucerquia HernándezDepartment of Medicine, George Washington University, Washington, DC, United States of America.
Leandro SierraCentro de Investigación, Clínica de la Costa SAS, Barranquilla, Atlántico, Colombia.
Maria Villanueva ColpasCentro de Investigación, Clínica de la Costa SAS, Barranquilla, Atlántico, Colombia.
Juan Carlos Perez HernandezCentro de Investigación, Clínica de la Costa SAS, Barranquilla, Atlántico, Colombia.
Andres Alberto Figueroa QuastCentro de Investigación, Clínica de la Costa SAS, Barranquilla, Atlántico, Colombia.
Joaquin Andres Calderon De BarrosCentro de Investigación, Clínica de la Costa SAS, Barranquilla, Atlántico, Colombia.
José Forero MejíaCentro de Investigación, Clínica de la Costa SAS, Barranquilla, Atlántico, Colombia.
Johan Penagos RuizCentro de Investigación, Clínica de la Costa SAS, Barranquilla, Atlántico, Colombia.
David BoyleDepartment of Medicine, UC San Diego School of Medicine, San Diego, CA, United States of America.
Gary S FiresteinDepartment of Medicine, UC San Diego School of Medicine, San Diego, CA, United States of America.
Gary L SimonDepartment of Medicine, George Washington University, Washington, DC, United States of America.
University of the Coast · COGeorge Washington University · USUniversidad Libre de Colombia · COMilken Institute · USUniversity of California San Diego · USHenry M. Jackson Foundation · USNorthwell Health · USUnited States Army Medical Research Institute of Infectious Diseases · US

Funding

The role of IL-2 therapy for Relapsing-Remitting Chikungunya ArthritisK23AR076505 · NIAMS · GEORGE WASHINGTON UNIVERSITY · PI CHANG, AILEEN · 2020 to 2022
$466k
NIAMS NIH HHS K23 AR076505
6 · The paper itself

Abstract

objectiveTo define the relationship between chronic chikungunya post-viral arthritis disease severity, cytokine response and T cell subsets in order to identify potential targets for therapy.

methodsParticipants with chikungunya arthritis were recruited from Colombia from 2019-2021. Arthritis disease severity was quantified using the Disease Activity Score-28 and an Arthritis-Flare Questionnaire adapted for chikungunya arthritis. Plasma cytokine concentrations (interleukin (IL)-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12p70, IL-13, interferon-γ and tumor necrosis factor (TNF)) were measured using a Meso Scale Diagnostics assay. Peripheral blood T cell subsets were measured using flow cytometry.

resultsAmong participants with chikungunya arthritis (N = 158), IL-2 levels and frequency of regulatory T cells (Tregs) were low. Increased arthritis disease activity was associated with higher levels of inflammatory cytokines (IL-6, TNF and CRP) and immunoregulatory cytokine IL-10 (p<0.05). Increased arthritis flare activity was associated with higher Treg frequencies (p<0.05) without affecting T effector (Teff) frequencies, Treg/Teff ratios and Treg subsets. Finally, elevated levels of IL-2 were correlated with increased Treg frequency, percent Tregs out of CD4+ T cells, and Treg subsets expressing immunosuppressive markers, while also correlating with an increased percent Teff out of live lymphocytes (p<0.05).

conclusionChikungunya arthritis is characterized by increased inflammatory cytokines and deficient IL-2 and Treg responses. Greater levels of IL-2 were associated with improved Treg numbers and immunosuppressive markers. Future research may consider targeting these pathways for therapy.

Indexed as

Arthritis, InfectiousChikungunya FeverCD4-Positive T-LymphocytesCross-Sectional StudiesCytokinesHumansImmunosuppressive AgentsInterleukin-10Interleukin-2Interleukin-6T-Lymphocytes, RegulatoryTumor Necrosis Factor-alphaCytokinesImmunosuppressive AgentsInterleukin-10Interleukin-2Interleukin-6Tumor Necrosis Factor-alpha

Identifiers

PMID38507338
PMCPMC10954186
OpenAlexW4393026229

What OpenQuestion holds

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LicenceCC0
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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.