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免疫刺激性 CpG 寡核苷酸:对基因表达的影响及其作为疫苗佐剂的应用。

Immunostimulatory CpG oligonucleotides: Effect on gene expression and utility as vaccine adjuvants.

机构信息

Cancer and Inflammation Program, National Cancer Institute, Frederick, MD 21702, United States.

出版信息

Vaccine. 2010 Feb 23;28(8):1919-23. doi: 10.1016/j.vaccine.2009.10.094.

Abstract

Synthetic oligodeoxynucleotides (ODN) containing unmethylated CpG motifs mimic the immunostimulatory activity of bacterial DNA. CpG ODN directly stimulate B cells and plasmacytoid dendritic cells (pDC), promote the production of Th1 and pro-inflammatory cytokines, and trigger the maturation/activation of professional antigen presenting cells. CpG ODN are finding use as vaccine adjuvants, where they increase the speed, magnitude and duration of vaccine-specific immune responses. For example, CpG ODN significantly prolong the protection induced by AVA (Anthrax Vaccine Adsorbed). Unexpectedly, a majority of animals immunized with CpG-adjuvanted AVA maintain resistance to anthrax infection even after their Ab titers decline to sub-protective levels. This survival is mediated by the de novo production of protective Abs by high affinity long-lived memory B cells. The immunostimulatory activity of CpG ODN was probed at the molecular level by microarray. Results show that a small group of 'inducers' rapidly up-regulated a large network genes following CpG treatment of mice. This stimulatory activity is quenched by 'suppressors' that down-regulate the expression of targeted genes, including most of the 'inducers'. These findings shed light on the mechanism underlying CpG-mediated immune activation and therapeutic activity.

摘要

合成的寡脱氧核苷酸(ODN)含有未甲基化的 CpG 基序,模拟细菌 DNA 的免疫刺激活性。CpG ODN 直接刺激 B 细胞和浆细胞样树突状细胞(pDC),促进 Th1 和促炎细胞因子的产生,并触发专业抗原呈递细胞的成熟/激活。CpG ODN 正在被用作疫苗佐剂,它们可以增加疫苗特异性免疫反应的速度、幅度和持续时间。例如,CpG ODN 显著延长了 AVA(炭疽疫苗吸附剂)诱导的保护作用。出乎意料的是,大多数用 CpG 佐剂 AVA 免疫的动物即使在抗体滴度下降到亚保护水平后仍能抵抗炭疽感染。这种存活是由高亲和力长寿记忆 B 细胞新产生的保护性抗体介导的。CpG ODN 的免疫刺激活性在分子水平上通过微阵列进行了探测。结果表明,一小部分“诱导剂”在 CpG 处理小鼠后迅速上调了一大组基因网络。这种刺激活性被“抑制剂”抑制,后者下调了靶向基因的表达,包括大多数“诱导剂”。这些发现为 CpG 介导的免疫激活和治疗活性的机制提供了线索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a78/2830905/28f53b525569/nihms156719f1.jpg

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