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

  • Ruolin Lu
  • , Chad Groer
  • , Peter A. Kleindl
  • , K. Ryan Moulder
  • , Aric Huang
  • , Jordan R. Hunt
  • , Shuang Cai
  • , Daniel J. Aires
  • , Cory Berkland
  • , M. Laird Forrest

Research output: Contribution to journalArticlepeer-review

77 Scopus citations

Abstract

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 α-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).

Original languageEnglish
Pages (from-to)165-176
Number of pages12
JournalJournal of Controlled Release
Volume306
DOIs
StatePublished - Jul 28 2019

Keywords

  • Cancer immunotherapy
  • Depot effect
  • Nanotherapeutic formulation
  • Sustained delivery
  • Toll-like receptor agonists

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