Evidence map›Paper›PMID 33857232›Full record

ArticlePloS one2021

Influence of the shared epitope on the elicitation of experimental autoimmune arthritis biomarkers.

Anastasios Karydis, Indra Sandal, Jiwen Luo, Amanda Prislovsky, Amanda Gamboa, Edward F Rosloniec, David D Brand

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 43% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Role of Citrullinated Collagen in Autoimmune Arthritis.International journal of molecular sciences · 2022
    Article
  3. Article
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 3 institutions in 1 country.

Anastasios KarydisDepartment of Periodontology, University of Tennessee Health Science Center, Memphis, TN, United States of America.
Indra SandalMemphis VA Medical Center, Memphis, TN, United States of America.
Jiwen LuoDepartment of Medicine, University of Tennessee Health Science Center, Memphis, TN, United States of America.
Amanda PrislovskyMemphis VA Medical Center, Memphis, TN, United States of America.
Amanda GamboaOregon State University, Corvallis, Oregon, United States of America.
Edward F RosloniecMemphis VA Medical Center, Memphis, TN, United States of America.
David D BrandMemphis VA Medical Center, Memphis, TN, United States of America.ORCID 0000-0002-9260-7963
University of Tennessee Health Science Center · USMemphis VA Medical Center · USOregon State University · US

Funding

Structure-function of HLA-DR, peptides, and T cells in autoimmune arthritisI01BX001045 · VA · MEMPHIS VA MEDICAL CENTER · PI ROSLONIEC, EDWARD F · 2011 to 2014
–
Neo-antigens and the function of HLA-DR alleles in autoimmune arthritisI01BX003256 · VA · MEMPHIS VA MEDICAL CENTER · PI ROSLONIEC, EDWARD F · 2017 to 2020
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Elucidating the Mechanisms that link the Shared Epitope, Periodontal Disease and ArthritisI01BX003487 · VA · MEMPHIS VA MEDICAL CENTER · PI BRAND, DAVID D. · 2017 to 2020
–
BLRD VA I01 BX001045BLRD VA I01 BX003256BLRD VA I01 BX003487
6 · The paper itself

Abstract

Our previous studies have shown that inoculation of the oral cavity of "humanized" B6.DR1/4 mice with the periodontal pathogen Porphyromonas gingivalis results in an increase in the percentage of circulating Th17 cells, loss of bone and an exacerbation of experimental autoimmune arthritis. The aim of this study was to assess the role played by the human HLA-DRβ molecule containing the shared epitope supplied as a transgene to I-A˚ (murine class II null) C57BL/6 (B6) mice in driving these findings. We compared various immune response parameters as well as alveolar and peri-articular bone loss between humanized B6.DR1 (or B6.DR4) mice and their WT (B6) counterparts. We found that the presence of the shared epitope in the context of inoculation with P. gingivalis enhanced the percentage of Th17 cells generated, dramatically enhanced bone loss and importantly allowed for the generation of CCP2⁺ ACPAs that are not found in C57BL/6 or DBA/1 arthritic mouse serum. Due to the exceedingly complex nature of environmental factors impacting on genetic elements, it has been difficult to unravel mechanisms that drive autoimmune arthritis in susceptible individuals. The findings in this study may provide one small piece of this puzzle that can help us to better understand part of this complexity.

Indexed as

EpitopesAlveolar Bone LossAnimalsArthritis, ExperimentalArthritis, RheumatoidBiomarkersHumansMicePorphyromonas gingivalisBiomarkersEpitopes

Identifiers

PMID33857232
PMCPMC8049293
OpenAlexW3155924015

What OpenQuestion holds

Textmetadata
LicenceCC0
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.