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Virology: Research and Treatment

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Intrabody-based Mapping of Latency-associated Nuclear Antigen from Kaposi’s Sarcoma-associated Herpesvirus  Show Conserved Epitopes for Viral Latency Inhibition

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Publication Date: 10 Mar 2010

Type: Original Research

Journal: Virology: Research and Treatment

Citation: Virology: Research and Treatment 2010:2 1-16

doi: 10.4137/VRT.S975

Abstract

Kaposi’s sarcoma associated herpesvirus (KSHV or human herpesvirus 8 [HHV-8]) is a gammaherpesvirus highly associated with KS, primary effusion lymphoma (PEL), and multicentric Castleman’s disease, an aggressive lymphoproliferative disorder. KSHV, like other gammaherpesvirus latently infects predominantly B-cells and endothelial cells. Infected cells retain the virus from one generation to the next existing as a multicopy circular episomal DNA in the nucleus, expressing a limited subset of viral genes. Of these latently expressed genes, LANA1, the latency associated nuclear antigen is highly expressed in all forms of KS-associated malignancies. Various studies so far show that LANA1 tethers the viral episomes to host chromosomes and binds to specific sites within and close to the TR elements contributing to the stable maintenance of the viral episomes in successive daughter cells. Anti-LANA1 intrabody strategies might represent a new therapeutic approach to treatment of KSHV infections, since LANA1 is regained for KSHV latency. In addition, the use of intrabodies can help drug development by mapping LANA1 inhibiting regions. We report development of several LANA1 specific single chain antibodies from immunized rabbits that can be expressed intracellularly, bind to LANA1 epitopes and can be used for functional KSHV studies on viral latency.


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We were invited to write a review article for Virology: Research and Treatment.  The review process was very quick and smooth and our interactions with Libertas Academica staff was clear, efficient and very personable.  I highly recommend publishing with this group.
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