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Development of TLR9 agonists for cancer therapy

机译:TLR9激动剂用于癌症治疗的开发

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摘要

In vertebrates, the TLRs are a family of specialized immune receptors that induce protective immune responses when they detect highly conserved pathogen-expressed molecules. Synthetic agonists for several TLRs, including TLR3, TLR4, TLR7, TLR8, and TLR9, have been or are being developed for the treatment of cancer. TLR9 detects the unmethylated CpG dinucleotides prevalent in bacterial and viral DNA but not in vertebrate genomes. As discussed in this Review, short synthetic oligodeoxynucleotides containing these immune stimulatory CpG motifs activate TLR9 in vitro and in vivo, inducing innate and adaptive immunity, and are currently being tested in multiple phase II and phase III human clinical trials as adjuvants to cancer vaccines and in combination with conventional chemotherapy and other therapies.
机译:在脊椎动物中,TLR是一类特殊的免疫受体,在检测到高度保守的病原体表达分子时会诱导保护性免疫反应。已经或正在开发针对几种TLR的合成激动剂,包括TLR3,TLR4,TLR7,TLR8和TLR9,以治疗癌症。 TLR9检测在细菌和病毒DNA中普遍存在的未甲基化的CpG二核苷酸,但在脊椎动物基因组中未检测到。如本评论所述,包含这些免疫刺激性CpG主题的短合成寡聚脱氧核苷酸可在体内和体外激活TLR9,诱导先天性和适应性免疫,目前正在II期和III期人类临床试验中作为癌症疫苗和佐剂的佐剂进行测试。结合常规化学疗法和其他疗法。

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    Krieg, Arthur M.;

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  • 年度 2007
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