Factor H, a regulator of complement activity, is a major determinant of meningococcal disease susceptibility in UK Caucasian patients

Scand J Infect Dis. 2006;38(9):764-71. doi: 10.1080/00365540600643203.

Abstract

Defence against Neisseria meningitidis involves complement-mediated bactericidal activity. Factor H (fH) down-regulates complement activation. A putatively functional single-nucleotide-polymorphism (SNP) exists within a presumed nuclear-factor-kappa-B responsive element (NF-kB) in the fH gene (C-496T). Genetic and functional investigations were carried out to determine whether C-496T has a role in meningococcal disease (MD) susceptibility. Genetic susceptibility was investigated in 2 independent studies, a case-control and family-based transmission-disequilibrium-test (TDT), using 2 separate cohorts of UK Caucasian patients. MD susceptibility was both genetically associated with the C/C homozygous genotype (OR = 2.0, 95% CI 1.3 - 3.2, p = 0.001) and linked to the C allele (p = 0.04), the association being most significant in serogroup C infected patients (OR = 2.9, 95% CI 1.6 - 5.5, p = 0.0002). FH serum concentrations were also associated with C-496T genotype, with highest fH concentrations in C/C homozygous individuals (p = 0.01). Functional studies showed NF-kappa-B binding to the C-496T-containing region and that pre-incubation of fH with meningococci reduced bactericidal activity and increased meningococci B and C survival in blood. This study shows that C-496T is both associated and linked with MD and that individuals possessing the fH C-496T C/C genotype are more likely to have increased serum fH protein levels, have reduced bactericidal activity against meningococci and be at an increased risk of contracting MD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Alleles
  • Blood Bactericidal Activity
  • Case-Control Studies
  • Child
  • Child, Preschool
  • Cohort Studies
  • Complement Factor H / analysis*
  • Complement Factor H / genetics*
  • Disease Susceptibility
  • Family Health
  • Genetic Predisposition to Disease*
  • Homozygote
  • Humans
  • Infant
  • Meningococcal Infections / genetics
  • Meningococcal Infections / immunology*
  • Middle Aged
  • NF-kappa B / metabolism
  • Polymorphism, Single Nucleotide*
  • Protein Binding
  • Statistics as Topic
  • United Kingdom
  • White People

Substances

  • NF-kappa B
  • Complement Factor H