Literature DB >> 9261432

Cell and viral regulatory elements enhance the expression and function of a human immunodeficiency virus inhibitory gene.

U Ranga1, C Woffendin, Z Y Yang, L Xu, S Verma, D R Littman, G J Nabel.   

Abstract

Regulated expression of recombinant genes in CD4+ cells is an important objective for gene therapy of AIDS, as these cells represent the principal target for viral replication of human immunodeficiency virus (HIV). We report here that specific combinations of CD4 cell-specific and viral regulatory elements can enhance expression of an antiviral gene product. Different viral regulatory elements were incorporated into a previously reported CD4 locus control region to increase the expression of reporter genes in T and monocytic cell lines. The CD4-specific regulatory elements were included to enhance expression in CD4 cells, and viral regulatory regions, including the cytomegalovirus immediate-early (CMV IE) upstream enhancer, which contains the kappa B and Ap1 regulatory elements and a Tat-responsive element of the HIV type 1 long terminal repeat, were used to increase gene expression and modulate its activity in response to viral infection. In transient transfection assays, this vector was 100- to 1,000-fold more active than the original CD4 regulatory elements alone. Expression of an inhibitory form of the Rev protein, Rev M10, was more effective than previously described vectors and protected against productive viral replication in CD4+ peripheral blood mononuclear cells. The combination of CD4 lineage-specific and viral regulatory elements will facilitate the development of more effective antiviral genetic strategies for AIDS.

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Year:  1997        PMID: 9261432      PMCID: PMC191988     

Source DB:  PubMed          Journal:  J Virol        ISSN: 0022-538X            Impact factor:   5.103


  72 in total

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2.  High-efficiency retroviral-mediated gene transfer into human and nonhuman primate peripheral blood lymphocytes.

Authors:  B A Bunnell; L M Muul; R E Donahue; R M Blaese; R A Morgan
Journal:  Proc Natl Acad Sci U S A       Date:  1995-08-15       Impact factor: 11.205

Review 3.  The human immunodeficiency virus: infectivity and mechanisms of pathogenesis.

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4.  High-efficiency transformation of mammalian cells by plasmid DNA.

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5.  T-cell activation. Transcriptional regulation in activated T cells.

Authors:  S Goodbourn
Journal:  Curr Biol       Date:  1994-10-01       Impact factor: 10.834

6.  Nonviral and viral delivery of a human immunodeficiency virus protective gene into primary human T cells.

Authors:  C Woffendin; Z Y Yang; L Xu; N S Yang; M J Sheehy; G J Nabel
Journal:  Proc Natl Acad Sci U S A       Date:  1994-11-22       Impact factor: 11.205

7.  Genetic modification of human peripheral blood lymphocytes with a transdominant negative form of Rev: safety and toxicity.

Authors:  B A Fox; C Woffendin; Z Y Yang; H San; U Ranga; D Gordon; J Osterholzer; G J Nabel
Journal:  Hum Gene Ther       Date:  1995-08       Impact factor: 5.695

8.  Inhibition of clinical human immunodeficiency virus (HIV) type 1 isolates in primary CD4+ T lymphocytes by retroviral vectors expressing anti-HIV genes.

Authors:  T VandenDriessche; M K Chuah; L Chiang; H K Chang; B Ensoli; R A Morgan
Journal:  J Virol       Date:  1995-07       Impact factor: 5.103

9.  Regulated expression of a dominant negative form of Rev improves resistance to HIV replication in T cells.

Authors:  J Liu; C Woffendin; Z Y Yang; G J Nabel
Journal:  Gene Ther       Date:  1994-01       Impact factor: 5.250

10.  Inhibition of HIV-1 Tat-mediated LTR transactivation and HIV-1 infection by anti-Tat single chain intrabodies.

Authors:  A M Mhashilkar; J Bagley; S Y Chen; A M Szilvay; D G Helland; W A Marasco
Journal:  EMBO J       Date:  1995-04-03       Impact factor: 11.598

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  1 in total

1.  Over-expression of the HIV-1 Rev promotes death of nondividing eukaryotic cells.

Authors:  Aviad Levin; Zvi Hayouka; Assaf Friedler; Abraham Loyter
Journal:  Virus Genes       Date:  2010-02-12       Impact factor: 2.332

  1 in total

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