Formulation and preclinical evaluation of a toll-like receptor 7/8 agonist as an anti-tumoral immunomodulator

被引:63
作者
Lu, Ruolin [1 ]
Groer, Chad [2 ]
Kleindl, Peter A. [1 ]
Moulder, K. Ryan [1 ]
Huang, Aric [1 ]
Hunt, Jordan R. [1 ]
Cai, Shuang [1 ,2 ]
Aires, Daniel J. [2 ,3 ]
Berkland, Cory [1 ,4 ]
Forrest, M. Laird [1 ,2 ]
机构
[1] Univ Kansas, Dept Pharmaceut Chem, Lawrence, KS 66045 USA
[2] HylaPharm LLC, Lawrence, KS USA
[3] Univ Kansas, Med Ctr, Sch Med, Div Dermatol, Kansas City, KS 66103 USA
[4] Univ Kansas, Dept Chem & Petr Engn, Lawrence, KS 66045 USA
关键词
Toll-like receptor agonists; Nanotherapeutic formulation; Depot effect; Sustained delivery; Cancer immunotherapy; VACCINE ADJUVANT ACTIVITY; IMMUNE-RESPONSES; VITAMIN-E; RECENT TRENDS; PRODRUG; INNATE; INHIBITION; ACTIVATION; DELIVERY; MODELS;
D O I
10.1016/j.jconrel.2019.06.003
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The toll-like receptor 7 and 8 (TLR7/8) agonist Resiquimod (R848) has been recognized as a promising immunostimulator for the treatment of cutaneous cancers in multiple clinical trials. However, systemic administration of R848 often results in strong immune-related toxicities while having limited therapeutic effects to the tumor. In the present study, a prodrug-based nanocarrier delivery system was developed that exhibited high therapeutic efficiency. R848 was conjugated to alpha-tocopherol to constitute an R848-Toco prodrug, followed by formulating with a tocopherol-modified hyaluronic acid (HA-Toco) as a polymeric nano-suspension. In vitro evaluation showed that the delivery system prolonged the release kinetics while maintaining TLR agonist activities. When administered subcutaneously, the nano-suspension formed a depot at the injection site, inducing localized immune responses without systemic expansion. This formulation also suppressed tumor growth and recruited immune cells to the tumor in a murine model of head and neck cancer. In a preclinical canine study of spontaneous mast cell tumors, the treatment led to a 67% response rate (three partial remissions and one complete remission).
引用
收藏
页码:165 / 176
页数:12
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