ABSTRACT
Background: Common variable immunodeficiency (CVID) is the most common symptomatic primary immunodeficiency. Certain gene loci are pointed out in several studies in CVID patients. Until now, monogenic defects have been identified in only 2-10% of CVID patients; therefore, association of the disease with HLA alleles may be important for elucidating immunological and genetic mechanisms behind CVID. The aim of this study is to investigate the relationship between CVID and HLA alleles. Methods: HLA class I/II alleles were analyzed in 65 patients with CVID and alleles that may be related to disease susceptibility were determined by comparing with 300 healthy controls. We also evaluated HLA allele frequencies in CVID patients with gastrointestial system (GIS) involvement and autoimmune manifestations. Results: When compared with controls, frequencies of B*27, B*35, C*04, and DRB1*04 alleles were significantly different in patients with CVID (p < .05). Frequencies of C*12, DRB1*13, and DRB1*15 alleles were more frequent in controls, indicating protective alleles (p < .05). There was a statistically significant difference for DQ2 and DQ8 haplotypes between patients with GIS involvement and controls. Conclusion: In comparison with literature, distinctive HLA alleles found in our study may originate from the diversity in gene pool between the populations. These data may provide clues for disease susceptibility.
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Acknowledgments
The authors thank patients and their families for their collaboration and participation. Also, we would like to thank the Scientific and Technological Research Council of Turkey (Project Number: 315S125).
Author contributions
Begum Ozbek, MSc, developed the theory, performed experiments, collected the data, contributed data or analysis tools, interpreted the data, wrote the paper.
Cagman Tan, PhD, provided key/unique reagents, performed experiments, and contributed data collection.
Ismail Yaz, MSc, contributed data collection and wrote the paper, contributed to the final version of the manuscript.
Can Kosukcu, MSc, analyzed the data and interpreted the data.
Saliha Esenboga, MD, contributed data collection and wrote the paper.
Pınar Gur Cetinkaya, MD, contributed data collection.
Deniz Cagdas Ayvaz, MD, PhD, supervised the study.
Ilhan Tezcan, MD, PhD, conceived, designed, and supervised the study.
Disclosure statement
The authors have declared no conflicting interests.
Data availability
The data are available from the corresponding author upon request.
Supplementary material
Supplemental data for this article can be accessed on the publisher’s website.