Detection of human herpesvirus 8 DNA and antibodies to latent nuclear and lytic-phase antigens in serial samples from aids patients with Kaposi’s sarcoma

Background: human herpesvirus 8 (HHV-8) have recently implicated in the etiology of Kaposi’s sarcoma (KS), but the pathophysiologic and immunologic interactions between HHV-8 and the human host are incompletely understood. Objective: this paper intends to present partial results of a follow-up study...

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Published inJournal of clinical virology Vol. 16; no. 3; pp. 247 - 251
Main Authors Camera Pierrotti, Lı́gia, Masami Sumita, Laura, Santos Freire, Wilton, Hehl Caiaffa Filho, Hélio, Akico Ueda Fick de Souza, Vanda
Format Journal Article Conference Proceeding
LanguageEnglish
Published Amsterdam Elsevier B.V 01.05.2000
Elsevier Science
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Summary:Background: human herpesvirus 8 (HHV-8) have recently implicated in the etiology of Kaposi’s sarcoma (KS), but the pathophysiologic and immunologic interactions between HHV-8 and the human host are incompletely understood. Objective: this paper intends to present partial results of a follow-up study of KS patients, designed to investigate HHV-8 viremia and antibody response. Methods: ninety-six paired serial samples (PBMCs and sera) were obtained from 12 aids patients with KS who received HAART prior or just after entry in the study. HHV-8 DNA was detected by nested-PCR and antibodies to HHV-8 latent nuclear antigen (LANA) and lytic antigen by immunofluorescence assay (IFA). Results: HHV-8 DNA was detected in 33.3% of the first PBMC samples. Among the eight PCR negative patients, four presented positive samples during the follow-up and four remained negative. Five patients had intermittent viremia. Fifteen of the 96 PBMC samples were PCR positive (15.6%). Four of 39 samples (10.2%) from patients classified as stadio II and 11 of the 53 samples (20.7%) from patients in stadio IV were PCR positive ( P=0.2). Six patients (50%) had anti-LANA antibodies at the entry in the study. Among the six seronegative patients, two seroconverted 2 months later and four patients remained seronegative during the 5–8 months of follow-up. All patients had anti-lytic antibodies since the first sample. Conclusion: the presence of HHV-8 viremia could be related to the severity of KS and could be intermittent even under HAART. A longer follow-up is needed to confirm these results.
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ISSN:1386-6532
1873-5967
DOI:10.1016/S1386-6532(99)00078-5