Serum levels and genetic variation of IL-35 are associated with multiple sclerosis: a population-based case-control study.


Journal

Immunologic research
ISSN: 1559-0755
Titre abrégé: Immunol Res
Pays: United States
ID NLM: 8611087

Informations de publication

Date de publication:
02 2022
Historique:
received: 12 05 2021
accepted: 10 10 2021
pubmed: 29 10 2021
medline: 3 5 2022
entrez: 28 10 2021
Statut: ppublish

Résumé

This study aimed to investigate the association between serum levels and polymorphic variants of IL-35 with susceptibility, clinical features, and disease severity in multiple sclerosis (MS) patients.This case-control study recruited 186 MS patients and 195 sex- and age-matched healthy controls. Serum levels and polymorphic variants of IL-35 were determined by ELISA and restriction fragment length polymorphism (RFLP)-PCR or high resolution melting (HRM) analysis methods, respectively. In addition, by in silico analysis, we evaluated the location and function of the polymorphism.Serum levels of IL-35 were significantly lower in the patients than those of healthy controls (49.3 ± 3.7 vs. 69.5 ± 7.8, p = 0.009). EBI3 rs4740 polymorphism of IL-35 was associated with 2.2-fold increased risk of MS susceptibility (95% CI, 1.3-3.9, p = 0.005). However, there were no differences in the genotype distribution and allele frequencies of IL-35 rs568408 between the patients and controls (p > 0.05). In silico results showed that variation in IL-12A and EBI3 may affect on protein pathways of the cells and different components of the immune system such as NF-κB and INF-γ.The results show that IL-35 polymorphisms might be a genetic risk factor for the development of MS.

Identifiants

pubmed: 34708312
doi: 10.1007/s12026-021-09246-9
pii: 10.1007/s12026-021-09246-9
doi:

Substances chimiques

Interleukins 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

75-85

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

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Auteurs

Mina Eslami (M)

Department of Immunology, Molecular and Cell Biology Research Center, School of Medicine, Mazandaran University of Medical Sciences, 4847191971, Sari, Iran.

Alireza Rafiei (A)

Department of Immunology, Molecular and Cell Biology Research Center, School of Medicine, Mazandaran University of Medical Sciences, 4847191971, Sari, Iran. rafiei1710@gmail.com.

Seyed Mohammad Baghbanian (SM)

Department of Neurology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.

Sadegh Fattahi (S)

Department of Genetics, Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.

Zahra Yazdani (Z)

Department of Immunology, Molecular and Cell Biology Research Center, School of Medicine, Mazandaran University of Medical Sciences, 4847191971, Sari, Iran.

Reza Valadan (R)

Department of Immunology, Molecular and Cell Biology Research Center, School of Medicine, Mazandaran University of Medical Sciences, 4847191971, Sari, Iran.

Mostafa Kardan (M)

Department of Immunology, Molecular and Cell Biology Research Center, School of Medicine, Mazandaran University of Medical Sciences, 4847191971, Sari, Iran.

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