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Elevated Virus Loads of Kaposi’s Sarcoma–Associated Human Herpesvirus 8 Predict Kaposi's Sarcoma Disease Progression, but Elevated Levels of Human Immunodeficiency Virus Type 1 Do Not
Author(s) -
E. Byrd Quinlivan,
Chuan Zhang,
Paul W. Stewart,
Chulaluk Komoltri,
Michelle G. Davis,
Robert S. Wehbie
Publication year - 2002
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/340652
Subject(s) - sarcoma , kaposi's sarcoma , virus , virology , polymerase chain reaction , peripheral blood mononuclear cell , viral load , immunology , medicine , real time polymerase chain reaction , viral disease , biomarker , gammaherpesvirinae , immunopathology , herpesviridae , pathology , biology , human herpesvirus , gene , biochemistry , in vitro
Kaposi's sarcoma-associated herpesvirus (KSHV) is found in Kaposi's sarcoma (KS), multicentric Castleman's disease, and primary effusion lymphomas. To prospectively evaluate KSHV load as a biomarker for KS clinical status and prognosis in a cohort of men with AIDS-related KS, 2 quantitative polymerase chain reaction (PCR) assays were developed and tested to determine KSHV peripheral blood mononuclear cell (PBMC) virus loads. Most patients (13/15) with good-prognosis KS had < or =1.5 log KSHV copies/10(5) PBMC by both quantitative competitive (QC) and real-time Applied Biosystems (ABI) PCR. Both assays provided 94% specificity for identifying the 16 patients without KS progression during 20 months of follow-up. QC-PCR and ABI-PCR exhibited 100% and 80% levels of diagnostic sensitivity, respectively, for identifying the 5 patients whose KS progressed. Neither dichotomized human immunodeficiency virus loads nor dichotomized CD4 counts predicted either KS progression or KS clinical stage (all positive predictive values < 30%). These results are evidence that the quantity of circulating KSHV in KS patients is biologically meaningful and is measurable with sufficient accuracy to provide clinically useful information.

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