Increased frequency of homozygosity of abnormal mannan-binding-protein alleles in patients with suspected immunodeficiency

Lancet. 1995 Oct 7;346(8980):941-3. doi: 10.1016/s0140-6736(95)91559-1.

Abstract

A low plasma concentration of mannan-binding protein (MBP) impairs opsonisation and phagocytosis. Three different mutations in the MBP gene have a dominant effect on MBP concentration. We investigated the frequency of the abnormal MBP alleles in 228 unrelated patients suspected of various non-HIV-related immunodeficiencies. The frequency of heterozygotes for the abnormal alleles was not different from that in the background population (36.0% and 37.4%, respectively). By contrast, the frequency of homozygotes for the abnormal alleles was significantly increased (8.3% and 0.8%, respectively; p = 0.0017). This finding implies that homozygotes for abnormal MBP alleles are predisposed to recurrent infections.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Carrier Proteins / blood
  • Carrier Proteins / genetics*
  • Child, Preschool
  • Collectins
  • Female
  • Gene Frequency
  • Homozygote
  • Humans
  • Immunologic Deficiency Syndromes / blood
  • Immunologic Deficiency Syndromes / genetics*
  • Infant
  • Male

Substances

  • Carrier Proteins
  • Collectins