AI Article Synopsis

  • The study investigates the link between IL17A gene polymorphism and the risk of developing BCG osteitis in individuals vaccinated as newborns.
  • Researchers analyzed gene polymorphisms and serum IL-17A levels in 132 adults who had BCG osteitis, comparing their data with 405 unvaccinated controls.
  • Findings indicated a significant difference in IL17A rs2275913 genotypes between the BCG osteitis patients and controls, suggesting that this polymorphism increases the risk of developing the condition post-vaccination.

Article Abstract

Aim: Interleukin-17 (IL-17) appears to promote the host's defence against mycobacterial infections. This study evaluated the association between IL17A gene polymorphism and the risk of Bacillus Calmette-Guérin (BCG) osteitis after newborn vaccination and between IL17A gene polymorphism and IL-17A concentrations in serum.

Methods: IL17A rs2275913 gene polymorphisms and serum IL-17A concentrations were studied in 132 adults aged 21-49 years from across Finland, who had BCG osteitis in infancy after a newborn BCG vaccination. The subjects were recruited in 2007-2008, and their whole-blood samples were sent to the National Institute for Health and Welfare, Turku, Finland. Their genotypes and minor allele frequencies were compared with 405 population-based unvaccinated controls aged two to three months from a prospective birth cohort study.

Results: The genotypes and allele frequencies of IL17A rs2275913 differed significantly between the former BCG osteitis patients and controls. The genotype was variant in 75.8% of cases and 64.0% of controls (p = 0.012), and the minor allele frequency was 50.0% in the cases and 41.6% of the controls (p = 0.009). Serum IL-17 concentrations did not differ significantly between the cases with wild or variant genotypes.

Conclusion: IL17A rs2275913 gene polymorphism was associated with a risk of BCG osteitis after vaccination.

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Source
http://dx.doi.org/10.1111/apa.14000DOI Listing

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