Reprogramming tumor microenvironment via systemic delivery of TLR3 agonist and manganese nanoparticle

Despite the promise of Toll-like receptor agonists as immune adjuvants, their antitumor efficacy has been limited in the clinic. Here, we report the development of a lipid nanoparticle system (PLCMP) designed for codelivery of a TLR3 agonist and Mn2+ and simultaneous activation of TLR3 and stimulato...

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Hauptverfasser: Cho, Young Seok, Zhou, Xingwu, Sun, Xiaoqi, Wan, Ziye, Crowther, Julia, Takahashi, Mariko, Kodamasimham, Swetha, Wu, Qi, Phoo, May Thazin, Na, Youngseo, Han, Kai, Li, Zaiye, Schwendeman, Anna, Schwendeman, Steven P., Lei, Yu Leo, Moon, James J.
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Sprache:eng
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Zusammenfassung:Despite the promise of Toll-like receptor agonists as immune adjuvants, their antitumor efficacy has been limited in the clinic. Here, we report the development of a lipid nanoparticle system (PLCMP) designed for codelivery of a TLR3 agonist and Mn2+ and simultaneous activation of TLR3 and stimulator of interferon genes (STING) pathways. Systemic administration of PLCMP in combination with α-PD-1 therapy led to strong antitumor effects in multiple murine tumor models. In addition, we have demonstrated the potential of the PLCMP platform to deliver tumor antigens and induce antigen-specific T cell responses, leading to improved cancer vaccination.
DOI:10.6084/m9.figshare.27103858