Jb. Black et al., EVALUATION OF IMMUNOASSAYS FOR DETECTION OF ANTIBODIES TO HUMAN HERPESVIRUS-7, Clinical and diagnostic laboratory immunology, 3(1), 1996, pp. 79-83
enzyme immunoassay (EIA), an immunoblot assay (IB), and an indirect im
munofluorescence assay were developed for detection of human herpesvir
us 7 (I4HV 7) antibodies in human serum. Cross-absorption studies with
EIA or IFA using HHV-7 and human herpesvirus 6 (HHV-6) antigens indic
ated that most human sera contain cross-reactive HHV-6 and HHV-7 antib
odies and that the degree of cross-reactivity varies between individua
l serum specimens. Inhibition of homologous antibody activity by absor
ption with heterologous virus ranged from 0 to 57% by EIA. However, fo
r every sample tested, absorption with homologous virus removed more a
ctivity than did heterologous virus, An 88-kDa protein was identified
as an HHV-7-specific serologic marker by IB. Activity to this protein
was not removed by absorption with HHV-6 antigen, Of the three assays,
the EIA was the most sensitive (94%), while the IB was the most speci
fic (94%). Approximately 80% of specimens collected from German adults
and children older than 2 years were positive for HHV-7 antibodies by
these assays.