从细菌到药物:用含有细菌DNA CpG序列的寡脱氧核苷酸进行治疗性免疫调节。

A. Krieg
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引用次数: 65

摘要

几种类型的免疫细胞具有模式识别受体(PRR),可以通过检测特定碱基背景(CpG基序)中未甲基化的CpG二核苷酸来区分原核DNA和脊椎动物DNA。含有这些CpG基序的细菌DNA或人工合成的寡脱氧核苷酸可激活先天和获得性免疫反应,这些免疫反应已进化为防止细胞内感染。这些T辅助性1 (Th1)样免疫反应包括B细胞、树突状细胞、巨噬细胞和自然杀伤细胞(NK)的激活。CpG dna诱导的免疫激活可以单独或与疫苗联合预防感染,在过敏性疾病和癌症的免疫治疗中是有效的。使用这种CpG DNA的人体临床试验目前正在进行中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
From bugs to drugs: therapeutic immunomodulation with oligodeoxynucleotides containing CpG sequences from bacterial DNA.
Several types of immune cells possess pattern recognition receptors (PRR) that can distinguish prokaryotic DNA from vertebrate DNA by detecting unmethylated CpG dinucleotides in particular base contexts (CpG motifs). Bacterial DNA or synthetic oligodeoxynucleotides containing these CpG motifs activate both innate and acquired immune responses that have evolved to protect against intracellular infections. These T helper 1 (Th1)-like immune responses include activation of B cells, dendritic cells, macrophages, and natural killer (NK) cells. CpG DNA-induced immune activation can protect against infection either alone or in combination with a vaccine and is effective in the immunotherapy of allergic diseases and cancer. Human clinical trials using such CpG DNA are currently underway.
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