| First Author | Zhou D | Year | 2019 |
| Journal | Cancer Biol Med | Volume | 16 |
| Issue | 2 | Pages | 288-298 |
| PubMed ID | 31516749 | Mgi Jnum | J:287153 |
| Mgi Id | MGI:6415506 | Doi | 10.20892/j.issn.2095-3941.2018.0309 |
| Citation | Zhou D, et al. (2019) Attenuated plasmodium sporozoite expressing MAGE-A3 induces antigen-specific CD8+ T cell response against lung cancer in mice. Cancer Biol Med 16(2):288-298 |
| abstractText | Objective: Cancer vaccines that rely on tumor antigen-specific CD8(+) T cell responses, are promising anti-cancer adjuvant immunotherapies. This study investigated whether genetically attenuated Plasmodium sporozoite (GAS) could be used as a novel vector to induce antigen-specific CD8(+) T cell responses against lung cancer. Methods: We constructed GAS/MAGE-A3, a recombinant GAS engineered to express the lung cancer-specific antigen, melanoma-associated antigen 3 (MAGE-A3), and assessed its therapeutic effects against lung cancer. Results: Robust parasite-specific CD8alpha(low)CD11a(high) and CD49d(high)CD11a(high) CD4(+) T cell responses as well as a MAGE-A3-specific CD8(+) T cell response were induced in GAS/MAGE-A3-immunized mice. Adoptive transfer of GAS/MAGE-A3-induced CD8(+) T cells from HLA-A2 transgenic mice into lung cancer-bearing nude mice inhibited tumor growth and prolonged survival. Conclusions: These findings demonstrate that GAS/MAGE-A3 induces a strong MAGE-A3-specific CD8(+) T cell response against lung cancer in vivo, and indicate that GAS is a novel and efficacious antigen delivery vector for antitumor immunotherapy. |
