| Literature DB >> 33191838 |
Fereshte Salami1,2, Saba Fekrvand2, Reza Yazdani2, Sepideh Shahkarami2,3,4, Gholamreza Azizi5, Yasser Bagheri6, Samaneh Delavari2, Sahar Shariati1,2, Seyed Alireza Mahdaviani7, Mohammamd Nabavi8, Afshin Shirkani9, Hassan Abolhassani10,11, Morteza Samadi1,12,13, Asghar Aghamohammadi2.
Abstract
Common variable immunodeficiency (CVID) is a primary immunodeficiency disease with a heterogeneous genetic background. Lipopolysaccharide-responsive beige-like anchor (LRBA), as well as cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), have important regulatory roles in the immune responses. Here, we have investigated the expression of LRBA and CTLA-4 proteins in CVID patients with at least one presentation of early-onset occurrence, autoimmunity, or enteropathy. In this study, 20 newly diagnosed CVID patients without infection only phenotype, and ten healthy individuals were enrolled. The expressions of LRBA and CTLA-4 proteins were assessed by western blotting and flow cytometry, respectively. The patients were divided into two groups of autoimmunity-positive (11 cases) and autoimmunity-negative (9 patients). LRBA and CTLA-4 expressions were significantly lower in autoimmune-positive patients than in healthy individuals (P = .03 and P = .03, respectively). Autoimmune-negative patients had lower expression of LRBA and CTLA-4 than the control group, although it was not significant. There was a positive correlation between the expressions of LRBA and CTLA-4 in both groups of patients (P < .05). Furthermore, the highest frequency of LRBA (85.7%) and CTLA-4 (71.4%) defects was detected in those with concomitant presence of autoimmunity, enteropathy, and early-onset occurrence. Concurrent presence of autoimmunity, enteropathy, and early-onset occurrence in CVID patients could be indicative of a lack of expression in LRBA and CTLA-4 proteins. This could be helpful in early diagnosis and initiation of appropriate treatment in these patients prior to genetic confirmation.Entities:
Keywords: Common variable immunodeficiency (CVID); autoimmunity; cytotoxic T lymphocyte-associated antigen-4 (CTLA-4); early-onset occurrence; enteropathy; lipopolysaccharide (LPS)-responsive beige-like anchor (LRBA)
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Year: 2020 PMID: 33191838 DOI: 10.1080/08820139.2020.1833029
Source DB: PubMed Journal: Immunol Invest ISSN: 0882-0139 Impact factor: 3.657