Lytic growth of Kaposi's sarcoma–associated herpesvirus (human herpesvirus 8) in culture

R Renne, W Zhong, B Herndier, M Mcgrath, N Abbey… - Nature medicine, 1996 - nature.com
R Renne, W Zhong, B Herndier, M Mcgrath, N Abbey, D Kedes, D Ganem
Nature medicine, 1996nature.com
Kaposi's sarcoma (KS) is the leading neoplasm of AIDS patients, and HIV infection is known
to be a major risk factor for its development1, 2. However, KS can occur in the absence of
HIV infection3–5 and the risk of KS development varies widely even among HIV–infected
patients, with homosexual men with AIDS being 20 times more likely to develop KS than
AIDS–afflicted children or hemophiliacs6. These and other data strongly suggest that a
sexually transmitted agent or co–factor may be involved in KS pathogenesis7. Recently …
Abstract
Kaposi's sarcoma (KS) is the leading neoplasm of AIDS patients, and HIV infection is known to be a major risk factor for its development1,2. However, KS can occur in the absence of HIV infection3–5 and the risk of KS development varies widely even among HIV–infected patients, with homosexual men with AIDS being 20 times more likely to develop KS than AIDS–afflicted children or hemophiliacs6. These and other data strongly suggest that a sexually transmitted agent or co–factor may be involved in KS pathogenesis7. Recently, DNA sequences corresponding to the genome of a novel member of the herpesvirus family have been identified within AIDS–KS biopsies8, and several reports indicate that these sequences are also present in all forms of HIV–negative KS (ref. 9–13). These and other findings14 suggest this new agent, referred to as KS–associated herpesvirus (KSHV) or human herpesvirus 8 (HHV8), as a candidate for the putative etiologic cofactor. However, the role of this agent in KS remains hotly debated15. Further progress in understanding its biology has been severely hampered by the lack of a cell culture system for virus growth. Here we report the development of a system for the lytic growth of this virus in a latently infected B cell line and present the first ultrastructural visualization of the virus. This system will facilitate the detailed study of the molecular biology of viral replication, the testing of antiviral drugs and the development of diagnostic tests for viral infection.
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