Adenosine triphosphate, polymyxin B and B16 cell-derived immunization induce anticancer response

被引:2
作者
Barrera-Avalos, Carlos [1 ,2 ]
Mena, Javier [1 ]
Lopez, Ximena [1 ]
Cappelli, Claudio [1 ,6 ]
Neira, Tanya [1 ]
Imarai, Monica [1 ,2 ]
Fernandez, Ricardo [3 ]
Robles-Planells, Claudia [1 ,2 ]
Rojo, Leonel E. [1 ,2 ]
Milla, Luis A. [4 ]
Leiva-Salcedo, Elias [1 ]
Escobar, Alejandro [5 ]
Acuna-Castillo, Claudio [1 ,2 ]
机构
[1] Univ Santiago Chile, USACH, Fac Quim & Biol, Dept Biol, Alameda 3363, Santiago, Chile
[2] Univ Santiago Chile, USACH, Ctr Biotecnol Acuicola, Alameda 3363, Santiago, Chile
[3] Univ Lagos, Dept Salud, Osorno, Chile
[4] Univ Santiago Chile, Fac Ciencias Med, Escuela Med, Ctr Invest Biomed & Aplica, Santiago, Chile
[5] Univ Chile, Fac Odontol, Inst Invest Ciencias Odontol, Santiago, Chile
[6] Univ Austral Chile, Inst Bioquim & Microbiol, Lab Patol Mol, Valdivia, Chile
关键词
anticancer; ATP; cost-effective; DAMPs; immunotherapy; melanoma; polymyxin B; P2X(7) RECEPTOR; CALRETICULIN EXPOSURE; DENDRITIC CELLS; TUMOR-GROWTH; IMMUNOGENICITY; AUTOPHAGY; DEATH;
D O I
10.2217/imt-2020-0209
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Aim: Whole dead tumor cells can be used as antigen source and the induction of protective immune response could be enhanced by damage-associated molecular patterns. Materials & methods: We generated whole dead tumor cells called B16-immunogenic cell bodies (ICBs) from B16 melanoma cells by nutrient starvation and evaluated the in vivo antitumor effect of B16-ICBs plus ATP and polymyxin B (PMB). Results: The subcutaneous immunization with B16-ICBs + PMB + ATP a 50% of tumor-free animals and induced a significant delay in tumor growth in a prophylactic approach. These results correlated with maturation of bone marrow-derived dendritic cells and activation of T CD8(+) lymphocytes in vitro. Conclusion: Altogether, ICB + ATP + PMB is efficient in inducing the antitumor efficacy of the whole dead tumor cells vaccine.
引用
收藏
页码:309 / 326
页数:18
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