| Literature DB >> 22297135 |
Kazushi Nakano1, Harutaka Katano, Kenjiro Tadagaki, Yuko Sato, Eriko Ohsaki, Yasuko Mori, Koichi Yamanishi, Keiji Ueda.
Abstract
Recent studies have indicated that vMIP-I and vMIP-II play important roles in the pathogenesis of Kaposi's sarcoma-associated herpesvirus (KSHV)-related diseases due to the effects of these proteins on vascularization. We developed monoclonal antibodies against KSHV-encoded viral macrophage inflammatory protein-I (vMIP-I) and vMIP-II to study these expression profiles and reveal the pathogenesis of KSHV-related diseases. The MAbs against vMIP-I and vMIP-II reacted to KSHV-infected cell lines after lytic induction. Both vMIP-I and the vMIP-II gene products were detected 24 h post-induction with 12-O-tetradecanoylphorbol-13-acetate until 60 h in the cytoplasm of primary effusion lymphoma cell lines. In clinical specimens, both vMIP-I and vMIP-II gene products were detected in the tissues of patients with multicentric Castleman's disease. On the other hand, only vMIP-II was detected in a subset of Kaposi's sarcoma. We concluded that these antibodies might be powerful tools to elucidate the pathogenesis of KSHV-related diseases. Copyright ÂEntities:
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Year: 2012 PMID: 22297135 DOI: 10.1016/j.virol.2012.01.008
Source DB: PubMed Journal: Virology ISSN: 0042-6822 Impact factor: 3.616