Identical point mutation leading to low levels of mannose binding protein and poor C3b mediated opsonisation in Chinese and Caucasian populations

Immunol Lett. 1992 May;32(3):253-7. doi: 10.1016/0165-2478(92)90058-v.

Abstract

A common opsonic defect occurring in 7% of the Caucasian population is associated with low serum levels of the lectin mannose binding protein (MBP). This study sought to determine whether the deficiency was also present in a Chinese population using sera obtained from 100 healthy Chinese children (age range 6 weeks-16 years). The distribution profiles of MBP levels and C3b/C3bi fragments binding to mannan coated plates were both bimodal and similar to the corresponding Caucasian profiles. Serum MBP levels were low in 9% of the Chinese children and all of these sera generated low levels of C3b/C3bi fragments. Overall there was a high significant correlation between MBP levels and C3b opsonin generation (r = 0.77; P less than 0.001). By analogy with similar findings in a Caucasian population we believe this correlation to be a reflection of antibody independent complement activation by MBP. In a pilot study of DNA obtained from three adult Chinese with low MBP levels the point mutation causing MBP deficiency in Caucasians was identified in all three cases.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Asian People / genetics
  • Carrier Proteins / analysis
  • Carrier Proteins / genetics*
  • Child
  • Child, Preschool
  • Complement C3b / analysis
  • Humans
  • Infant
  • Infant, Newborn
  • Mannose-Binding Lectins
  • Mutagenesis, Site-Directed
  • Opsonin Proteins / blood
  • White People / genetics

Substances

  • Carrier Proteins
  • Mannose-Binding Lectins
  • Opsonin Proteins
  • Complement C3b