Major Histocompatibility Complex Class II

Autoimmune disease fibromyalgia human leukocyte antigen inflammation major histocompatibility complex protective epitope rheumatoid arthritis susceptibility epitope

Journal

Recent advances in inflammation & allergy drug discovery
ISSN: 2772-2716
Titre abrégé: Recent Adv Inflamm Allergy Drug Discov
Pays: Netherlands
ID NLM: 101776469

Informations de publication

Date de publication:
2022
Historique:
received: 29 11 2021
revised: 28 12 2021
accepted: 11 01 2022
pubmed: 24 3 2022
medline: 15 12 2022
entrez: 23 3 2022
Statut: ppublish

Résumé

Preliminary evidence has pointed an association of the gene HLA-DRB1 with fibromyalgia. HLA-DRB1 alleles carrying the shared or susceptibility epitope encoding the five-amino acid motif QKRAA, QRRAA or RRRAA in positions 70 to 74 of the major histocompatibility complex class II DRβ chain are associated with several autoimmune diseases. The objective of this study was to test the hypothesis that susceptibility epitope-encoding HLA-DRB1 alleles are associated with fibromyalgia. Using a case-control design, the prevalence of susceptibility epitope-encoding HLADRB1 alleles in 27 white Caucasian patients fulfilling the revised diagnostic criteria for fibromyalgia of the American College of Rheumatology was compared with that in 27 white Caucasian ageand sex-matched healthy controls. 13 (48%) of the fibromyalgia patients had susceptibility epitope-coding HLA-DRB1 alleles compared with 15 (56%) of the controls (P = 0.785). The DRB1*01 allele encoding the protective epitope 70-DERAA-74 motif was found in one of the control subjects; none of the fibromyalgia patients had such a protective epitope. While the present study does not provide evidence supporting the potential role of HLA-DRB1 in the etiology of fibromyalgia, it does not exclude the possibility that there is a polygenic component to a putative genetic causative role.

Sections du résumé

BACKGROUND BACKGROUND
Preliminary evidence has pointed an association of the gene HLA-DRB1 with fibromyalgia. HLA-DRB1 alleles carrying the shared or susceptibility epitope encoding the five-amino acid motif QKRAA, QRRAA or RRRAA in positions 70 to 74 of the major histocompatibility complex class II DRβ chain are associated with several autoimmune diseases.
OBJECTIVE OBJECTIVE
The objective of this study was to test the hypothesis that susceptibility epitope-encoding HLA-DRB1 alleles are associated with fibromyalgia.
METHODS METHODS
Using a case-control design, the prevalence of susceptibility epitope-encoding HLADRB1 alleles in 27 white Caucasian patients fulfilling the revised diagnostic criteria for fibromyalgia of the American College of Rheumatology was compared with that in 27 white Caucasian ageand sex-matched healthy controls.
RESULTS RESULTS
13 (48%) of the fibromyalgia patients had susceptibility epitope-coding HLA-DRB1 alleles compared with 15 (56%) of the controls (P = 0.785). The DRB1*01 allele encoding the protective epitope 70-DERAA-74 motif was found in one of the control subjects; none of the fibromyalgia patients had such a protective epitope.
CONCLUSION CONCLUSIONS
While the present study does not provide evidence supporting the potential role of HLA-DRB1 in the etiology of fibromyalgia, it does not exclude the possibility that there is a polygenic component to a putative genetic causative role.

Identifiants

pubmed: 35319406
pii: RAIAD-EPUB-121776
doi: 10.2174/2772270816666220321162802
doi:

Substances chimiques

Epitopes 0
HLA-DRB1 Chains 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

16-18

Informations de copyright

Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

Références

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R: A Language and Environment for Statistical Computing R Core Team2021
JASP (Version 015) JASP Team2021
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Auteurs

Basant K Puri (BK)

Department of Molecular Biology and Medicine, University of Winchester, Winchester, UK.

Gary S Lee (GS)

Department of Medicine, University of Southampton, Southampton, United Kingdom.

Armin Schwarzbach (A)

Arminlabs, Department of Molecular Pathology, Augsburg, Germany.

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Classifications MeSH