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DNA, but not protein vaccine based on mutated BORIS antigen significantly inhibits tumor growth and prolongs the survival of mice

Abstract

The ideal immunological target for cancer vaccine development would meet the criteria of tumor specificity, immunogenicity and vital dependency of the tumor on the functional activities of the antigenic target so as to avoid antigenic loss by mutation. Given that at face value the brother of regulator of imprinted sites (BORIS) transcription factor meets these criteria, we have developed a mutant variant of this molecule (mBORIS) that lacks tumorigenic ability, while retaining immunogenic epitopes that elicits responses against histologically irrelevant tumor cells. Here we compared vaccine strategies employing as an immunogen either mBORIS recombinant protein formulated in a strong Th1-type adjuvant, QuilA or DNA encoding this immunogen along with plasmids expressing interleukin (IL)12/IL18 molecular adjuvants. In both groups of vaccinated mice induction of tumor-specific immunity (antibody response, T-cell proliferation, cytokine production, T-cell cytotoxicity) as well as ability to inhibit growth of the aggressive breast cancer cell line and to prolong survival of vaccinated animals have been tested. We determined that DNA, but not recombinant protein vaccine, induced potent Th1-like T-cell recall responses that significantly inhibited tumor growth and prolongs the survival of vaccinated mice. These studies demonstrate that DNA immunization is superior to recombinant protein strategy and provide a clear guidance for clinical development of a cancer vaccine targeting what appears to be a universal tumor antigen.

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References

  1. Gattinoni L, Powell Jr DJ, Rosenberg SA, Restifo NP . Adoptive immunotherapy for cancer: building on success. Nat Rev Immunol 2006; 6: 383–393.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  2. Vieweg J, Su Z, Dahm P, Kusmartsev S . Reversal of tumor-mediated immunosuppression. Clin Cancer Res 2007; 13: 727s–732s.

    Article  CAS  PubMed  Google Scholar 

  3. Biragyn A, Tani K, Grimm MC, Weeks S, Kwak LW . Genetic fusion of chemokines to a self tumor antigen induces protective, T-cell dependent antitumor immunity. Nat Biotechnol 1999; 17: 253–258.

    Article  CAS  PubMed  Google Scholar 

  4. Kim JJ, Trivedi NN, Wilson DM, Mahalingam S, Morrison L, Tsai A et al. Molecular and immunological analysis of genetic prostate specific antigen (PSA) vaccine (published erratum appears in Oncogene 1999 Apr 8;18(14):2411). Oncogene 1998; 17: 3125–3135.

    Article  CAS  PubMed  Google Scholar 

  5. Cohen EP . Cancer therapy with DNA-based vaccines. Immunol Lett 2000; 74: 59–65.

    Article  CAS  PubMed  Google Scholar 

  6. Monzavi-Karbassi B, Hennings LJ, Artaud C, Liu T, Jousheghany F, Pashov A et al. Preclinical studies of carbohydrate mimetic peptide vaccines for breast cancer and melanoma. Vaccine 2007; 25: 3022–3031.

    Article  CAS  PubMed  Google Scholar 

  7. Monzavi-Karbassi B, Artaud C, Jousheghany F, Hennings L, Carcel-Trullols J, Shaaf S et al. Reduction of spontaneous metastases through induction of carbohydrate cross-reactive apoptotic antibodies. J Immunol 2005; 174: 7057–7065.

    Article  CAS  PubMed  Google Scholar 

  8. Petrovan RJ, Kaplan CD, Reisfeld RA, Curtiss LK . DNA vaccination against VEGF receptor 2 reduces atherosclerosis in LDL receptor-deficient mice. Arterioscler Thromb Vasc Biol 2007; 27: 1095–1100.

    Article  CAS  PubMed  Google Scholar 

  9. Kaplan CD, Kruger JA, Zhou H, Luo Y, Xiang R, Reisfeld RA . A novel DNA vaccine encoding PDGFRbeta suppresses growth and dissemination of murine colon, lung and breast carcinoma. Vaccine 2006; 24: 6994–7002.

    Article  CAS  PubMed  Google Scholar 

  10. Scanlan MJ, Simpson AJ, Old LJ . The cancer/testis genes: review, standardization, and commentary. Cancer Immun 2004; 4: 1.

    PubMed  Google Scholar 

  11. Simpson AJ, Caballero OL, Jungbluth A, Chen YT, Old LJ . Cancer/testis antigens, gametogenesis and cancer. Nat Rev Cancer 2005; 5: 615–625.

    Article  CAS  PubMed  Google Scholar 

  12. Zendman AJ, Ruiter DJ, Van Muijen GN . Cancer/testis-associated genes: identification, expression profile, and putative function. J Cell Physiol 2003; 194: 272–288.

    Article  CAS  PubMed  Google Scholar 

  13. Klenova EM, Morse III HC, Ohlsson R, Lobanenkov VV . The novel BORIS+CTCF gene family is uniquely involved in the epigenetics of normal biology and cancer. Semin Cancer Biol 2002; 12: 399–414.

    Article  CAS  PubMed  Google Scholar 

  14. Loukinov DI, Pugacheva E, Vatolin S, Pack SD, Moon H, Chernukhin I et al. BORIS, a novel male germ-line-specific protein associated with epigenetic reprogramming events, shares the same 11-zinc-finger domain with CTCF, the insulator protein involved in reading imprinting marks in the soma. Proc Natl Acad Sci USA 2002; 99: 6806–6811.

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  15. Loukinov D, Ghochikyan A, Mkrtichyan M, Ichim TE, Lobanenkov VV, Cribbs DH et al. Antitumor efficacy of DNA vaccination to the epigenetically acting tumor promoting transcription factor BORIS and CD80 molecular adjuvant. J Cell Biochem 2006; 98: 1037–1043.

    Article  CAS  PubMed  Google Scholar 

  16. Vatolin S, Abdullaev Z, Pack SD, Flanagan PT, Custer M, Loukinov DI et al. Conditional expression of the CTCF-Paralogous transcriptional factor BORIS in normal cells results in demethylation and derepression of MAGE-A1 and reactivation of other cancer-testis genes. Cancer Res 2005; 65: 7751–7762.

    Article  CAS  PubMed  Google Scholar 

  17. Hong JA, Kang Y, Abdullaev Z, Flanagan PT, Pack SD, Fischette MR et al. Reciprocal binding of CTCF and BORIS to the NY-ESO-1 promoter coincides with derepression of this cancer-testis gene in lung cancer cells. Cancer Res 2005; 65: 7763–7774.

    Article  CAS  PubMed  Google Scholar 

  18. Ghochikyan A, Mkrtichyan M, Loukinov D, Mamikonyan G, Pack SD, Movsesyan N et al. Epigenetically acting tumor promoting transcription factor BORIS is widely expressed TAA inducing anti-tumor specific T cell responses. J Immunol 2007; 178: 556–573.

    Article  Google Scholar 

  19. Wang H, Hosiawa KA, Min W, Yang J, Zhang X, Garcia B et al. Cytokines regulate the pattern of rejection and susceptibility to cyclosporine therapy in different mouse recipient strains after cardiac allografting. J Immunol 2003; 171: 3823–3836.

    Article  CAS  PubMed  Google Scholar 

  20. Mills CD, Kincaid K, Alt JM, Heilman MJ, Hill AM . M-1/M-2 macrophages and the Th1/Th2 paradigm. J Immunol 2000; 164: 6166–6173.

    Article  CAS  PubMed  Google Scholar 

  21. Miller FR, Miller BE, Heppner GH . Characterization of metastatic heterogeneity among subpopulations of a single mouse mammary tumor: heterogeneity in phenotypic stability. Invasion Metastasis 1983; 3: 22–31.

    CAS  PubMed  Google Scholar 

  22. Aslakson CJ, Miller FR . Selective events in the metastatic process defined by analysis of the sequential dissemination of subpopulations of a mouse mammary tumor. Cancer Res 1992; 52: 1399–1405.

    CAS  PubMed  Google Scholar 

  23. Lelekakis M, Moseley JM, Martin TJ, Hards D, Williams E, Ho P et al. A novel orthotopic model of breast cancer metastasis to bone. Clin Exp Metastasis 1999; 17: 163–170.

    Article  CAS  PubMed  Google Scholar 

  24. Pulaski BA, Ostrand-Rosenberg S . Reduction of established spontaneous mammary carcinoma metastases following immunotherapy with major histocompatibility complex class II and B7.1 cell-based tumor vaccines. Cancer Res 1998; 58: 1486–1493.

    CAS  PubMed  Google Scholar 

  25. Pulaski BA, Terman DS, Khan S, Muller E, Ostrand-Rosenberg S . Cooperativity of Staphylococcal aureus enterotoxin B superantigen, major histocompatibility complex class II, and CD80 for immunotherapy of advanced spontaneous metastases in a clinically relevant postoperative mouse breast cancer model. Cancer Res 2000; 60: 2710–2715.

    CAS  PubMed  Google Scholar 

  26. Prehn RT . On the nature of cancer and why anticancer vaccines don't work. Cancer Cell Int 2005; 5: 25.

    Article  PubMed Central  PubMed  Google Scholar 

Download references

Acknowledgements

This work was supported in part by NIAID intramural grant and was also supported by NIH RO1 grants AI-44809, AG-20241 and NS-050895.

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Correspondence to M G Agadjanyan.

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Mkrtichyan, M., Ghochikyan, A., Loukinov, D. et al. DNA, but not protein vaccine based on mutated BORIS antigen significantly inhibits tumor growth and prolongs the survival of mice. Gene Ther 15, 61–64 (2008). https://doi.org/10.1038/sj.gt.3303044

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