Evidence map›Paper›PMID 34576893›Full record

ArticleMicroorganisms2021

A Mouse Model for Studying Post-Acute Arthritis of Chikungunya.

Aileen Y Chang, Sarah R Tritsch, Abigail J Porzucek, Arnold M Schwartz, Margaux Seyler-Schmidt, Arielle Glass, Patricia S Latham, St Patrick Reid, Gary L Simon, Christopher N Mores

Open access · goldAbstract read
In one paragraph

Article in Microorganisms, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

9 citing papers in PubMed, 13 citations in OpenAlex.

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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 3 institutions in 1 country.

Aileen Y ChangDepartment of Medicine, School of Medicine and Health Sciences, George Washington University, 2150 Pennsylvania Ave 5-416, Washington, DC 20037, USA.ORCID 0000-0001-7410-9867
Sarah R TritschDepartment of Global Health, Milken Institute School of Public Health, George Washington University, Washington, DC 20052, USA.
Abigail J PorzucekDepartment of Global Health, Milken Institute School of Public Health, George Washington University, Washington, DC 20052, USA.
Arnold M SchwartzDepartment of Pathology, School of Medicine and Health Sciences, George Washington University, Washington, DC 20037, USA.
Margaux Seyler-SchmidtDepartment of Global Health, Milken Institute School of Public Health, George Washington University, Washington, DC 20052, USA.ORCID 0000-0001-7831-8877
Arielle GlassDepartment of Global Health, Milken Institute School of Public Health, George Washington University, Washington, DC 20052, USA.
Patricia S LathamDepartment of Pathology, School of Medicine and Health Sciences, George Washington University, Washington, DC 20037, USA.ORCID 0000-0003-2782-9444
St Patrick ReidDepartment of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE 68182, USA.
Gary L SimonDepartment of Medicine, School of Medicine and Health Sciences, George Washington University, 2150 Pennsylvania Ave 5-416, Washington, DC 20037, USA.
Christopher N MoresDepartment of Global Health, Milken Institute School of Public Health, George Washington University, Washington, DC 20052, USA.
Milken Institute · USGeorge Washington University · USUniversity of Nebraska Medical Center · 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 AR076505NIAMS NIH HHS K23AR076505Pharmaceutical Research and Manufacturers of America Foundation Research Starter Grant
6 · The paper itself

Abstract

Chikungunya virus (CHIKV) was introduced to the Americas in 2013, causing two million infections across over thirty countries. CHIKV causes a chronic debilitating arthritis in one fourth of infected individuals and currently evidence-based targeted therapies for the treatment of CHIKV arthritis are lacking. Multiple mouse models of chikungunya have been developed to study acute CHIKV infection. In humans, post-CHIKV arthritis may persist for months to years after viremia from a CHIKV infection has resolved. Therefore, the development of a mouse model of post-acute arthritis of chikungunya may facilitate the study of potential novel therapeutics for this arthritis. In this article we describe the development of a wild-type immunocompetent C57BL/6 mouse model for post-acute arthritis of chikungunya, including a histologic inflammation scoring system, as well as suggestions for how this mouse model may be used to examine the efficacy of novel therapies for CHIKV arthritis.

Indexed as

arthritisarthritis therapybone erosionchikungunyamouse modelmyositissynovitis

Identifiers

PMID34576893
PMCPMC8470089
OpenAlexW3201534357

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.