Literature DB >> 15647772

Regulated and constitutive expression of anti-inflammatory cytokines by nontransforming herpesvirus saimiri vectors.

C Wieser1, D Stumpf, C Grillhösl, D Lengenfelder, S Gay, B Fleckenstein, A Ensser.   

Abstract

Herpesviral saimiri-(HVS) mediated expression of bovine growth hormone was one of the first applications of an episomal viral vector for gene therapy. Meanwhile, the long-term persistence of HVS vectors has been confirmed in a broad spectrum of infectable target cells in vitro and in vivo. Regulated gene expression is useful for many applications of gene therapy. Therefore, we inserted the Mifepristone-antiprogestin-inducible expression system (GeneSwitchtrade mark) into HVS viral vectors to regulate the combined expression of anti-inflammatory cytokines, IL-10 and IL-1RA. Constitutive CMV-promoter/enhancer-driven and Mifepristone-inducible cytokine expression was compared in the viral context in transduced primary human fibroblasts and rheumatoid arthritis (RA) fibroblast-like cells (RASF). Long-term persistence of vector genomes was shown for both construct types. Constitutive expression was efficient and more rapid in onset than in the inducible system, in which the selective induction of interleukin expression along with low background levels was obtained by Mifepristone concentrations that were more than 1000-fold below those required for endogenous Progesterone antagonism. Furthermore, transgene expression corresponded to vector doses. Global patterns of cytokine secretion were not significantly changed due to viral transduction, indicating a rather inert behavior of the viral vector itself. In an attempt to emulate the inflammatory cytokine-enriched environment in rheumatoid arthritic joints, the function of the vectors could be demonstrated in vitro by the successful blockade of IL-1beta-stimulated matrix-metalloproteinase (MMP)-3 expression from RASF cells. Evaluation of this system in future studies, in suitable long-term SCID models of RA or in non-human primate models, will exploit the possible in vivo benefits of nontransforming HVS vectors in gene therapy.

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Year:  2005        PMID: 15647772     DOI: 10.1038/sj.gt.3302424

Source DB:  PubMed          Journal:  Gene Ther        ISSN: 0969-7128            Impact factor:   5.250


  5 in total

1.  An improved Tet-On regulatable FasL-adenovirus vector system for lung cancer therapy.

Authors:  Isaac Sipo; Almudena Hurtado Picó; Xiaomin Wang; Jürgen Eberle; Iver Petersen; Stefan Weger; Wolfgang Poller; Henry Fechner
Journal:  J Mol Med (Berl)       Date:  2005-12-31       Impact factor: 4.599

2.  Inhibition of retromer activity by herpesvirus saimiri tip leads to CD4 downregulation and efficient T cell transformation.

Authors:  Dior Kingston; Heesoon Chang; Armin Ensser; Hye-Ra Lee; Jongsoo Lee; Sun-Hwa Lee; Jae Ung Jung; Nam-Hyuk Cho
Journal:  J Virol       Date:  2011-08-17       Impact factor: 5.103

3.  Growth transformation of human T cells by herpesvirus saimiri requires multiple Tip-Lck interaction motifs.

Authors:  Elke Heck; Ute Friedrich; Michaela U Gack; Doris Lengenfelder; Monika Schmidt; Ingrid Müller-Fleckenstein; Bernhard Fleckenstein; Armin Ensser; Brigitte Biesinger
Journal:  J Virol       Date:  2006-10       Impact factor: 5.103

4.  Potential of herpesvirus saimiri-based vectors to reprogram a somatic Ewing's sarcoma family tumor cell line.

Authors:  Hannah F Brown; Christian Unger; Adrian Whitehouse
Journal:  J Virol       Date:  2013-04-17       Impact factor: 5.103

5.  Mutation of herpesvirus Saimiri ORF51 glycoprotein specifically targets infectivity to hepatocellular carcinoma cell lines.

Authors:  Susan J Turrell; Adrian Whitehouse
Journal:  J Biomed Biotechnol       Date:  2010-12-09
  5 in total

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