Evaluation of MicroRNA-125b-5p and Transcription Factors BLIMP1 and IRF4 Expression in Unsolved Common Variable Immunodeficiency Patients.
Adult
Biomarkers
/ metabolism
Case-Control Studies
Common Variable Immunodeficiency
/ genetics
Down-Regulation
Epigenesis, Genetic
Female
Gene Expression Regulation
Humans
Interferon Regulatory Factors
/ genetics
Male
MicroRNAs
/ metabolism
Positive Regulatory Domain I-Binding Factor 1
/ genetics
Up-Regulation
Common Variable Immunodeficiency
Epigenesis
MicroRNAs
Primary immunodeficiency diseases;
Journal
Iranian journal of allergy, asthma, and immunology
ISSN: 1735-5249
Titre abrégé: Iran J Allergy Asthma Immunol
Pays: Iran
ID NLM: 101146178
Informations de publication
Date de publication:
08 Dec 2021
08 Dec 2021
Historique:
received:
28
03
2021
accepted:
23
06
2021
entrez:
18
12
2021
pubmed:
19
12
2021
medline:
8
3
2022
Statut:
epublish
Résumé
Common variable immunodeficiency (CVID) is the most prevalent form of symptomatic primary humoral immunodeficiencies characterized by failure in the final differentiation of B lymphocytes. The majority of CVID cases have no identified genetic defect, and epigenetic alteration could be involved in the pathogenesis of CVID. Hence, we aimed to evaluate the expression of hsa-miR-125b-5p -and, B lymphocyte-induced maturation protein-1(BLIMP-1) and interferon regulatory protein-4 (IRF-4) in a group of CVID patients with no definitive genetic diagnosis in comparison with healthy individuals. Ten CVID patients (all known genes excluded) and 10 age and sex-matched healthy controls participated in the study. B lymphocytes were isolated and expression of miR-125b-5p, IRF4, and BLIMP1 were evaluated by real-time polymerase chain reaction (RT-PCR). Moreover, B cell subsets were analyzed by flow cytometry. The results showed that the relative expression of miR-125b-5p in CVID patients was increased while it was decreased for the BLIMP1 and IRF4 transcription factors compared with the healthy controls. Although a reduction was observed in switched and non-switched memory B cells among all high-miR patients, these subsets were decreased in patients with normal miR expression (71.0% and 85.0%, respectively). Our results suggest that overexpression of miR-125b-5p affects the terminal differentiation of B cells in a selected group of CVID patients by downregulating the BLIMP-1 gene and more intensively for the IRF-4 gene expressions.
Identifiants
pubmed: 34920653
doi: 10.18502/ijaai.v20i6.8021
doi:
Substances chimiques
Biomarkers
0
Interferon Regulatory Factors
0
MIRN125 microRNA, human
0
MicroRNAs
0
interferon regulatory factor-4
0
PRDM1 protein, human
138415-26-6
Positive Regulatory Domain I-Binding Factor 1
EC 2.1.1.-
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM