Cb. Hall et al., PERSISTENCE OF HUMAN-HERPESVIRUS-6 ACCORDING TO SITE AND VARIANT - POSSIBLE GREATER NEUROTROPISM OF VARIANT-A, Clinical infectious diseases, 26(1), 1998, pp. 132-137
Little is known of the persistence and pathogenicity of human herpesvi
rus 6 (HHV-6) after primary infection, including the role of strain va
riant. Over 2 to 5 years, 2,716 children and 149 families were studied
. Peripheral blood mononuclear cell (PBMC), saliva, and cerebrospinal
fluid (CSF) specimens were examined for HHV-6 DNA and variant, Ninety-
nine percent of isolates causing primary infection were HHV-6 variant
B (HHV-6B), which predominated in 95%-98% of the variants persisting i
n PBMC and saliva specimens from children and adults. Of 668 CSF sampl
es, 13% contained HHV-6 DNA; of 77 children examined after primary inf
ection, 61% had HHV-6 DNA detected only in their CSF and 39% had HHV-6
DNA in both CSF and PBMCs. HHV-6 variant A (HHV-6A) was detected sign
ificantly (P = .0001) more frequently in CSF than in PBMCs or saliva.
in children for whom HHV-6 was identified in both CSF and PBMCs, PBMCs
contained only HHV-6B, while CSF contained HHV-6A or HHV-6B, not both
. Thus, in patients with dual infection, only HHV-6A persisted in CSF,
which suggests that HHV-6A has greater neurotropism. Findings for adu
lts indicate that dual infection occurs; variant persistence is simila
r to that for children, The frequency of HHV-6A infection increased li
ttle with age, thereby indicating that HHV-6A infection remains uncomm
on into adulthood. This study suggests that HHV-6 variants have differ
ent immunobiologic courses and neurotropism.