| Literature DB >> 32056073 |
Ismail Yaz1, Begum Ozbek1, Yuk Yin Ng2, Pinar Gur Cetinkaya1, Sevil Oskay Halacli1, Cagman Tan1, Merve Kasikci3, Can Kosukcu4, Ilhan Tezcan1,5, Deniz Cagdas6,7.
Abstract
Common variable immunodeficiency (CVID) results in defective B cell differentiation and impaired antibody production and is the most common symptomatic primary immunodeficiency. Our aim was to evaluate the correlation among B cell subgroups, κ-deleting recombination excision circle (KREC) copy numbers, and clinical and immunological data of the patients with CVID, and evaluate the patients according to classifications currently available to define the role of KREC copy numbers in the diagnosis of CVID. KREC analysis was performed using a quantitative real-time polymerase chain reaction assay, and B cell subgroups were measured by flow cytometry. The median age of the patients (n = 30) was 25 (6-69) years. Parental consanguinity ratio was 33%. The median age at diagnosis was 15 (4-59), and follow-up period was 6 (1-37) years. CD19+ and CD4+ cell counts at the time of diagnosis were low in 66.7% and 46.7% of the patients, respectively. CD19+ cell counts were positively correlated with KREC copy numbers in patients and healthy controls. CD19+ cell counts and KREC copy numbers were significantly reduced in CVID patients compared to healthy controls as expected. KRECs are quantitative markers for B cell defects. We found low CD4+ cell numbers, recent thymic emigrants, and lymphopenia in some of the patients at diagnosis, which reminds the heterogeneity of CVID's etiology. In this study, a positive correlation was shown between CD19+ cell counts and KREC copy numbers. Low KREC copy numbers indicated B cell deficiency; however, high KREC copy numbers were not sufficient to rule out CVID.Entities:
Keywords: B cells; CVID; Flow cytometry; KRECs; qRT-PCR
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Year: 2020 PMID: 32056073 DOI: 10.1007/s10875-020-00761-2
Source DB: PubMed Journal: J Clin Immunol ISSN: 0271-9142 Impact factor: 8.317