Association Between Cytometric Biomarkers, Clinical Phenotype, and Complications of Common Variable Immunodeficiency

• Published in: Curēus (Palo Alto, CA) CA), 2024-01, Vol.16 (1), p.e52941-e52941
• Main Authors: Markocsy, Adam, Bobcakova, Anna, Petrovicova, Otilia, Kapustova, Lenka, Malicherova Jurkova, Eva, Schniederova, Martina, Petriskova, Jela, Cibulka, Michal, Hyblova, Michaela, Jesenak, Milos
• Format: Article
• Language: English
• Subjects: Antigens; Bone marrow; Classification; Disease; Flow cytometry; Genes; Genotype & phenotype; Immune system; Infections; Laboratories; Lymphatic system; Lymphocytes; Monoclonal antibodies; Steroids; Ultrasonic imaging
• ISSN: 2168-8184; 2168-8184
• DOI: 10.7759/cureus.52941

Common variable immunodeficiency (CVID) is a heterogeneous group of immune disorders. The patients are classified according to the clinical manifestation with the infection-only phenotype (CVID ) and CVID with immune dysregulation (CVID ). We performed a retrospective clinical analysis of 64 CVID patients (34 males, 53.13%; mean age: 41.4 years; SD: ±21.4 years). We divided the patients into subgroups according to the clinical manifestation (CVID and CVID ) and according to B cell phenotypic profiling after performing flow cytometry with the use of the EUROclass classification. We compared clinical manifestations, selected laboratory parameters, and therapy in these groups. All CVID patients were tested after the manifestation of complications associated with immune dysregulation and in eight patients during the immunosuppressive treatment (systemic corticosteroids and hydroxychloroquine). Two-thirds of patients in our cohort had symptoms resulting from immune dysregulation. Almost half of the patients had autoimmune complications. A higher proportion of marginal zone B cells was associated with autoimmune complications. A lower percentage of naïve B cells was connected to autoimmunity, whereas a lower proportion of transitional B cells was associated with rheumatic diseases and splenomegaly. Patients with lymphadenopathy had a higher percentage of double-negative T cells and a lower percentage of switched memory B cells. We performed molecular-genetic testing in 28% (n = 17) of patients and found a causal pathogenic variant in 23.5% (n = 4) of this group. Based on our results, there is an association between specific cytometric parameters, clinical phenotype, and complications of CVID. The use of the subpopulations of B cells can be helpful in the diagnosis of these specific clinical complications in CVID patients and could help to personalise the therapeutic approach.