4.4 Article

Oral Administration of Poly-Gamma-Glutamic Acid Significantly Enhances the Antitumor Effect of HPV16 E7-Expressing Lactobacillus casei in a TC-1 Mouse Model

Journal

JOURNAL OF MICROBIOLOGY AND BIOTECHNOLOGY
Volume 29, Issue 9, Pages 1444-1452

Publisher

KOREAN SOC MICROBIOLOGY & BIOTECHNOLOGY
DOI: 10.4014/jmb.1906.06021

Keywords

Poly-gamma-glutamic acid; adjuvant; Lactobacillus casei; HPV16 E7; cervical cancer; natural killer cells

Funding

  1. R&D Convergence Program of the National Research Council of Science & Technology (NST) of the Republic of Korea [CAP-16-02-KIST]
  2. National Research Foundation of Korea (NRF) - Korea government [2018M3A9H4055203]
  3. National Research Council of Science & Technology (NST), Republic of Korea [CAP-16-02-KIST] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  4. National Research Foundation of Korea [2018M3A9H4055203] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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The conventional prophylactic vaccines for human papillomavirus (HPV) efficiently prevent infection with high-risk HPV types, but they do not promote therapeutic effects against cervical cancer. Previously, we developed HPV16 E7-expressing Lactobacillus casei (L. casei-E7) as a therapeutic vaccine candidate for cervical cancer, which induces antitumor therapeutic effects in a TC-1 murine cancer model. To improve the therapeutic effect of L. casei-E7, we performed co-treatment with poly-gamma-glutamic acid (gamma-PGA), a safe and edible biomaterial naturally secreted by Bacillus subtilis. We investigated their synergistic effect to improve antitumor efficacy in a murine cancer model. The treatment with gamma-PGA did not show in vitro cytotoxicity against TC-1 tumor cells; however, an enhanced innate immune response including activation of dendritic cells was observed. Mice co-administered with gamma-PGA and L. casei-E7 showed significantly suppressed growth of TC-1 tumor cells and an increased survival rate in TC-1 mouse models compared to those of mice vaccinated with L. casei-E7 alone. The administration of gamma-PGA markedly enhanced the activation of natural killer (NK) cells but did not increase the E7-specific cytolytic activity of CD8(+) T lymphocytes in mice vaccinated with L. casei-E7. Overall, our results suggest that oral administration of gamma-PGA induces a synergistic antitumor effect in combination with L. casei-E7.

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