Mannose-binding lectin concentrations, MBL2 polymorphisms, and susceptibility to respiratory tract infections in young men

J Infect Dis. 2008 Oct 15;198(8):1247-53. doi: 10.1086/591912.

Abstract

Background: Mannose-binding lectin (MBL) is an important component of innate immunity, and its deficiency is associated with susceptibility to recurrent infections.

Methods: This exploratory study investigated the association of serum MBL concentrations and MBL2 gene polymorphisms with respiratory tract infections in young men. We genotyped 6 single-nucleotide polymorphisms (SNPs) in the promoter region (alleles H/L, X/Y, and P/Q) and exon 1 (variant alleles B, C, and D and wild-type allele A) of the MBL2 gene by real-time polymerase chain reaction and measured serum MBL concentrations in 111 Finnish military recruits with asthma and 362 without.

Results: An MBL level below the median concentration was a significant risk factor for infections (asthma status-adjusted odds ratio [OR], 2.5 [95% confidence interval {CI}, 1.4-4.5]). Among the 6 SNPs, there was a significant association between the promoter Y/Y genotype and infections (OR, 2.3 [95% CI, 1.2-4.4]) and a borderline significant association between exon 1 variant alleles and infections (OR, 1.7 [95% CI, 0.9-3.1]), after adjustment for asthma status.

Conclusion: These preliminary results suggest, for the first time, an association between MBL level and respiratory tract infections in young men and a possible association between infections and MBL2 polymorphisms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Asthma / complications
  • Asthma / genetics
  • Exons / genetics
  • Finland
  • Genetic Predisposition to Disease*
  • Humans
  • Male
  • Mannose-Binding Lectin / blood*
  • Mannose-Binding Lectin / genetics
  • Military Personnel
  • Polymorphism, Single Nucleotide*
  • Promoter Regions, Genetic / genetics
  • Respiratory Tract Infections / genetics*
  • Respiratory Tract Infections / immunology

Substances

  • MBL2 protein, human
  • Mannose-Binding Lectin