Bastyr University, Kenmore, WA, USA.
Expert Rev Clin Pharmacol. 2011 Mar;4(2):275-89. doi: 10.1586/ecp.11.5.
Toll-like receptor (TLR) ligation activates both the innate and adaptive immune systems, and plays an important role in antiviral and anti-tumor immunity. Therefore, a significant amount of effort has been devoted to exploit the therapeutic potential of TLR agonists. Depending on the therapeutic purpose, either as adjuvants to vaccine, chemotherapy or standalone therapy, TLR agonists have been administered via different routes. Both preclinical and clinical studies have suggested that the route of administration has significant effects on pharmacokinetics, and that understanding these effects is critical to the success of TLR agonist drug development. This article will summarize the pharmacokinetics of TLR agonists with different administration routes, with an emphasis on clinical studies of TLR ligands in oncologic applications.
Toll 样受体 (TLR) 配体激活先天和适应性免疫系统,在抗病毒和抗肿瘤免疫中发挥重要作用。因此,人们投入了大量精力来开发 TLR 激动剂的治疗潜力。根据治疗目的,无论是作为疫苗、化疗或单独治疗的佐剂,TLR 激动剂都通过不同的途径给药。临床前和临床研究均表明,给药途径对药代动力学有显著影响,了解这些影响对于 TLR 激动剂药物开发的成功至关重要。本文将总结不同给药途径的 TLR 激动剂的药代动力学,重点介绍 TLR 配体在肿瘤学应用中的临床研究。