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Cationic liposomes conjugation to recombinant adenoviral vectors containing herpes simplex virus thymidine kinase gene followed by ganciclovir treatment reduces viral antigenicity and maintains antitumor activity in mouse experimental glioma models

Abstract

Gene therapy using adenoviral (Ad) vector containing herpes simplex virus thymidine kinase (AxCAHSV-tk) followed by the administration of ganciclovir (GCV) has been a promising therapy for cancer including malignant gliomas. However, there remain numerous problems to overcome, such as the high immunogenicity and toxicity of Ad vector. To optimize the therapy, we investigated whether a conjugation of our original cationic liposomes and Ad vectors reduces viral antigenicity and maintains the antitumor activity in mouse experimental (subcutaneous and intracranial) glioma models. Our original liposomes consist of N-(α-trimethylammonioacetyl)-didodecyl-D-glutamate chloride, dilauroyl phosphatidylcholine, and dioleoyl phosphatidyl-ethanolamine in a molar ratio of 1:2:2. AxCAHSV-tk and GCV showed a remarkable inhibition of experimental glioma growth. The growth-inhibitory effect decreased in mice previously immunized with another Ad vector (AxCALacZ). In contrast, the conjugation of AxCAHSV-tk and liposomes did not diminish the growth-inhibitory effect. Furthermore, the conjugation reduced antigenicity for Ad vector in vivo. These findings suggest that suicide gene therapy, using a conjugation of AxCAHSV-tk and our liposomes, is a feasible approach for human cancer gene therapy, especially malignant gliomas.

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References

  1. Ryuke Y, Mizuno M, Natsume A et al. The transduction efficiency of adenoviral vectors increases by associating with cationic liposomes on human glioma cells Neurol Med Chir (Tokyo) 2000 40: 256–260

    Article  CAS  Google Scholar 

  2. Natsume A, Mizuno M, Ryuke Y et al. Cationic liposomes conjugation to recombinant adenoviral vector reduces viral antigenicity Jpn J Cancer Res 2000 91: 363–367

    Article  CAS  Google Scholar 

  3. Wilkins RH, Ketcham AS . Studies of glioma in mice: 1. Experiments concerning glioma growth and hepatic mitotic activity J Natl Cancer Inst 1964 32: 871–880

    Google Scholar 

  4. Oldfield EH, Ram Z, Culver KW et al. Gene therapy for the treatment of brain tumors using intra-tumoral transduction with the thymidine kinase gene and intravenous ganciclovir Hum Gene Ther 1993 4: 39–69

    Article  CAS  Google Scholar 

  5. Ram Z, Culver KW, Oshiro EM et al. Therapy of malignant brain tumors by intratumoral implantation of retroviral vector-producing cells Nat Med 1997 3: 1354–1361

    Article  CAS  Google Scholar 

  6. Beer SJ, Matthews CB, Stein CS et al. Poly (lactic–glycolic) acid copolymer encapsulation of recombinant adenovirus reduced immunogenicity in vivo Gene Ther 1998 5: 740–746

    Article  CAS  Google Scholar 

  7. Kreuzer J, Denger S, Reifers F et al. Adenovirus-assisted lipofection: efficient in vitro gene transfer of luciferase and cytosine deaminase to human smooth muscle cells Atherosclerosis 1996 124: 49–60

    Article  CAS  Google Scholar 

  8. Raja-Walia R, Webber J, Naftilan J, Chapman GD, Naftilan AJ . Enhancement of liposome-mediated gene transfer into vascular tissue by replication deficient adenovirus Gene Ther 1995 2: 521–530

    CAS  PubMed  Google Scholar 

  9. Rainov NG, Ikeda K, Qureshi NH et al. Intraarterial delivery of adenovirus vectors and liposome–DNA complexes to experimental brain neoplasms Hum Gene Ther 1999 20: 311–318

    Article  Google Scholar 

  10. Lambright ES, Force SD, Lanuti ME et al. Efficacy of repeated adenoviral suicide gene therapy in a localized murine tumor model Ann Thorac Surg 2000 70: 1865–1870

    Article  CAS  Google Scholar 

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Correspondence to Masaaki Mizuno.

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Mizuno, M., Ryuke, Y. & Yoshida, J. Cationic liposomes conjugation to recombinant adenoviral vectors containing herpes simplex virus thymidine kinase gene followed by ganciclovir treatment reduces viral antigenicity and maintains antitumor activity in mouse experimental glioma models. Cancer Gene Ther 9, 825–829 (2002). https://doi.org/10.1038/sj.cgt.7700503

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