Evidence map›Paper›PMID 20061955›Full record

ReviewCurrent opinion in rheumatology2010

The rheumatoid arthritis HLA-DRB1 shared epitope.

Joseph Holoshitz

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in rheumatology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed, 3 pooled it
9.0field-weighted citation impact, top 2% 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

96 citing papers in PubMed, 3 syntheses or guidelines pooled it, 211 citations in OpenAlex.

  1. Pooled it
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  18. Frontiers in immunology · 2025
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36 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

1 author at 1 institution in 1 country.

Joseph HoloshitzDepartment of Internal Medicine, University of Michigan, Ann Arbor, 48109-5680, USA. jholo@umich.edu
University of Michigan–Ann Arbor · US

Funding

Vector CoreP30AR048310 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FOX, DAVID ALAN · 2001 to 2010
$5.9M
Immune Modulating HLA-Coded Ligands in Rheumatoid ArthritisR01AR059085 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HOLOSHITZ, JOSEPH · 2011 to 2020
$3.8M
UNIVERSITY OF MICHIGAN MULTIPURPOSE ARTHRITIS CENTERP60AR020557 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI IGNELZI, MICHAEL A · 1986 to 2001
$2.9M
A Class II MHC-Associated Lymphocyte Activation DefectR01AI047331 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HOLOSHITZ, JOSEPH · 2002 to 2006
$1.5M
Class II MHC Allele-Specific Signaling: A New Paradigm in Disease PathogenesisR01GM088560 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HOLOSHITZ, JOSEPH · 2009 to 2012
$1.2M
MHC class II-Associated Endothelial DysfunctionR21AR056786 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HOLOSHITZ, JOSEPH · 2009 to 2010
$379k
Immune dysregulation by the rheumatoid arthritis shared epitopeR21AR055170 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HOLOSHITZ, JOSEPH · 2008 to 2009
$367k
SHARED-USE RESEARCH COMPUTERS10RR002498 · NCRR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CLARK, VIRGINIA A. · 1985 to 1985
–
NCRR NIH HHS UL1RR02498NIAID NIH HHS AI47331NIAID NIH HHS R01 AI047331NIAMS NIH HHS AR20557NIAMS NIH HHS AR48310NIAMS NIH HHS AR55170NIAMS NIH HHS P30 AR048310NIAMS NIH HHS R01 AR059085NIAMS NIH HHS R21 AR055170NIAMS NIH HHS R21 AR056786NIGMS NIH HHS GM088560NIGMS NIH HHS R01 GM088560
6 · The paper itself

Abstract

purpose of reviewTo update progress made between December 2008 and November 2009 on the role of the rheumatoid arthritis (RA)-shared epitope in the cause and pathogenesis of RA. RECENT

findingsNew evidence has been recently presented to suggest that noninherited human leukocyte antigens (HLAs) originating through pregnancy or exposure to maternal antigens in utero could contribute to RA development in shared epitope-negative women. An interaction between smoking and shared epitope-coding non-*04 HLA-DRB1 alleles (particularly HLA-DRB1*01 and HLA-DRB1*10) was formally established for the first time. Progress has been made in determining the relative contributions and the interaction of the shared epitope, PTPN22 and smoking in conferring the risk of anticitrullinated protein antibodies-positive and negative RA. The autoantigen that anticitrullinated protein antibodies recognize in a significant number of RA patients has been identified as citrullinated alpha-enolase and the importance of genetic factors in anticitrullinated protein antibodies-negative RA has been highlighted. Additionally, associations of RA risk with several new genetic markers have been reported. Among them: two new major histocompatibility complex, non-DRB1 loci, a polymorphism marker in major histocompatibility complex class I polypeptide-related sequence A, an allele of the Fcgamma receptor, a polymorphism marker in the beta2-adrenergic receptor and a low-inducible allele of the cytochrome P450 subtype 1A2. SUMMARY: Although the mechanistic basis of shared epitope-RA association remains an enigma, observations made during the last year shed new light on the conditions in which the shared epitope - alone or in combination with other genes or environmental factors - affects the risk of RA and the phenotype of the disease.

Indexed as

Arthritis, RheumatoidAutoantibodiesBiomarkersEpitopesGenetic MarkersHLA-DR AntigensHLA-DRB1 ChainsHumansPolymorphism, GeneticProtein Tyrosine Phosphatase, Non-Receptor Type 22AutoantibodiesBiomarkersEpitopesGenetic MarkersHLA-DR AntigensHLA-DRB1 ChainsProtein Tyrosine Phosphatase, Non-Receptor Type 22PTPN22 protein, human

Identifiers

PMID20061955
PMCPMC2921962
OpenAlexW2092071745

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Registered trials

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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.