Department of Tumor Immunology, Radboud Institute for Molecular Life Sciences , Radboud University Medical Center , 6525 GA Nijmegen , The Netherlands.
Department of Chemistry , University of California, Irvine , Irvine , California 92697 , United States.
Bioconjug Chem. 2018 Mar 21;29(3):587-603. doi: 10.1021/acs.bioconjchem.7b00808. Epub 2018 Feb 16.
Toll-like receptors (TLRs) are vital elements of the mammalian immune system that function by recognizing pathogen-associated molecular patterns (PAMPs), bridging innate and adaptive immunity. They have become a prominent therapeutic target for the treatment of infectious diseases, cancer, and allergies, with many TLR agonists currently in clinical trials or approved as immunostimulants. Numerous studies have shown that conjugation of TLR agonists to other molecules can beneficially influence their potency, toxicity, pharmacokinetics, or function. The functional properties of TLR agonist conjugates, however, are highly dependent on the ligation strategy employed. Here, we review the chemical structural requirements for effective functional TLR agonist conjugation. In addition, we provide similar analysis for those that have yet to be conjugated. Moreover, we discuss applications of covalent TLR agonist conjugation and their implications for clinical use.
Toll 样受体 (TLRs) 是哺乳动物免疫系统的重要组成部分,通过识别病原体相关分子模式 (PAMPs) 来发挥作用,连接先天免疫和适应性免疫。它们已成为治疗感染性疾病、癌症和过敏的重要治疗靶点,许多 TLR 激动剂目前正在临床试验中或被批准为免疫刺激剂。许多研究表明,将 TLR 激动剂与其他分子缀合可以有益地影响它们的效力、毒性、药代动力学或功能。然而,TLR 激动剂缀合物的功能特性高度依赖于所采用的连接策略。在这里,我们回顾了有效功能 TLR 激动剂缀合的化学结构要求。此外,我们还对那些尚未缀合的 TLR 激动剂进行了类似的分析。此外,我们还讨论了 TLR 激动剂共价缀合的应用及其对临床应用的意义。