We assessed the genetic polymorphism of mannose-binding lectin (MBL) i
n 93 patients with chronic hepatitis C (45 responders and 48 nonrespon
ders to interferon) and 218 healthy controls. Mutant allele was identi
fied only at codon 54 (Gly --> Asp), leading to three genotypes (54 m/
m, 54 W/m, and 54 W/W). Frequency of 54 m/m was significantly lower in
interferon-responders (2.2%), compared to those in nonresponders (14.
6%) and controls (10.6%): p<0.05. Our results suggest that homozygous
carriage of the variant allele of codon 54 of MBL may predict poor res
ponse to interferon in chronic hepatitis C patients.