T. Hohler et al., NO ASSOCIATION BETWEEN MANNOSE-BINDING LECTIN ALLELES AND SUSCEPTIBILITY TO CHRONIC HEPATITIS-B VIRUS-INFECTION IN GERMAN PATIENTS, Experimental and clinical immunogenetics, 15(3), 1998, pp. 130-133
Variants of the mannose-binding lectin (MBL) have been shown to be ass
ociated with low serum concentrations of the protein and to predispose
to bacterial, fungal and viral infections. A recent small study on 33
Caucasian patients had suggested that a mutation at codon 52 of the M
BL gene is associated with chronic hepatitis B virus (HBV) infection.
Exon 1 of the MBL gene was amplified by PCR in 61 patients with chroni
c HBV infection, 28 patients with acute infection and in 60 controls,
MBL variants were detected by subsequent restriction enzyme digestion
and agarose gel electrophoresis, The occurrence of the codon 52 mutati
on in patients with chronic HBV infection did not differ significantly
from that in controls or patients with acute infection (9 vs, 7%), no
r were there any significant differences for the codon 54 mutation. Th
e frequency of MBL variants at codon 52 and 54 is not increased in pat
ients with chronic HBV infection. Thus, the previously reported associ
ation of MBL deficiency with chronic HBV infection in adults could not
be confirmed.