Patients with autoimmune chronic active hepatitis (AICAH) and certain
other chronic liver disorders often have very high titres of haemagglu
tination-inhibition (HI) antibodies to rubella virus. In this study it
is shown, using floatation centrifugation, that the high rubella HI r
eactivity is not caused by nonspecific lipoprotein inhibitors but rath
er by antibodies specific for the rubella haemagglutinin (E1 glycoprot
ein). After sucrose density gradient ultracentrifugation of sera the m
ajor HI reactivity was recovered in the IgG containing fractions. The
IgG antibody fraction was strongly reactive by an indirect enzyme-link
ed immunosorbent assay (ELISA). Higher prevalence and titres of rubell
a antibodies were also demonstrated by the complement fixation (CF) te
st using a haemagglutinin-free antigen, and by an indirect haemaggluti
nation (IHA) test (Rubacell) using a cell-associated antigen which is
distinct from the antigens used in the HI and CF tests. This high rube
lla antibody response is therefore demonstrated using th ree distinct
antigen-antibody systems. By means of absorption experiments and radio
immunoprecipitation assays the coating antigen used in the IHA test wa
s shown to reside in the E2 glycoprotein. The cause of this enhanced a
ntibody response to rubella virus structural proteins remains elusive.
(C) 1994 Wiley-Liss. Inc.