Purpose. Biliary glycoprotein (BGP), a member of the carcinoembryonic antig
en (CEA) gene family, is produced by hepatocytes, and is suggested to funct
ion as a cell adhesion molecule, mouse hepatitis virus receptor, and tumor
suppressor. Our aim was to establish an enzyme immunoassay for circulating
BGP and to study its significance in liver diseases. Methods. For enzyme im
munoassay, a monoclonal antibody (mAb), TS135, which recognizes BGP was use
d as a catcher, and biotin-labeled polyclonal anti-CEA antibodies were used
as a tracer. Seventy-six serum specimens obtained from patients with vario
us liver diseases were submitted to the assay. Results. The incidence of po
sitivity for antigen TS135 in the serum samples of the 76 patients was 57.9
%. The most significant correlation among conventional liver function tests
was found between antigen TS135 and gamma -glutamyl transpeptidase (I-GTP)
. However; among the 56 patients whose serum antigen TS135 and gamma -GTP l
evels could be measured simultaneously, 5 were antigen TS135-positive and g
amma -GTP-negative (8.9%) and 6 were antigen TS135-negative and gamma -GTP-
positive (10.7%). The increased serum level of antigen TS135 in 6 cholangio
cellular carcinoma (CCC) patients led us to the immunohistochemical study o
f CCC; in which 8 of the 8 tissue specimens tested were positive for mAb TS
135, indicating the production of the antigen from CCCs. Conclusions. This
preliminary study suggests that the circulating antigen TS135 level correla
tes with gamma -GTP in liver diseases, but that TS135 may also have a uniqu
e significance, different from that of gamma -GTP, as a liver function test
.