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从病菌到药物:利用含细菌DNA中CpG序列的寡脱氧核苷酸进行治疗性免疫调节

From bugs to drugs: therapeutic immunomodulation with oligodeoxynucleotides containing CpG sequences from bacterial DNA.

作者信息

Krieg A M

机构信息

Department of Veterans Affairs Medical Center, Iowa City, IA 52246, USA.

出版信息

Antisense Nucleic Acid Drug Dev. 2001 Jun;11(3):181-8. doi: 10.1089/108729001300338717.

Abstract

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.

摘要

几种免疫细胞拥有模式识别受体(PRR),这些受体可通过检测特定碱基环境(CpG基序)中未甲基化的CpG二核苷酸,将原核生物DNA与脊椎动物DNA区分开来。含有这些CpG基序的细菌DNA或合成寡脱氧核苷酸可激活先天性和获得性免疫反应,这些反应的进化目的是抵御细胞内感染。这些类似辅助性T细胞1(Th1)的免疫反应包括B细胞、树突状细胞、巨噬细胞和自然杀伤(NK)细胞的激活。CpG DNA诱导的免疫激活单独使用或与疫苗联合使用时均可预防感染,并且在过敏性疾病和癌症的免疫治疗中有效。目前正在进行使用此类CpG DNA的人体临床试验。

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