Klinman Dennis M, Currie Debra, Gursel Ihsan, Verthelyi Daniela
Section of Retroviral Immunology, Division of Viral Products, Center for Biologics Evaluation and Research, Food and Drug Administration, Bethesda, MD 20892, USA.
Immunol Rev. 2004 Jun;199:201-16. doi: 10.1111/j.0105-2896.2004.00148.x.
Synthetic oligodeoxynucleotides (ODNs) containing unmethylated CpG motifs directly stimulate human B cells and plasmacytoid dendritic cells (pDCs), thereby promoting the production of T helper 1 (Th1) and pro-inflammatory cytokines and the maturation/activation of professional antigen-presenting cells. These activities enable CpG ODNs to act as immune adjuvants, accelerating and boosting antigen-specific immune responses by 5-500-fold. These effects are optimized by maintaining close physical contact between the CpG DNA and the immunogen. Animal challenge models establish that protective immunity can be accelerated and magnified by coadministering CpG DNA with vaccines. Ongoing clinical studies indicate that CpG ODNs are safe and well tolerated when administered as adjuvants to humans, and in some cases, they increase vaccine-induced immune responses.
含有未甲基化CpG基序的合成寡脱氧核苷酸(ODN)可直接刺激人B细胞和浆细胞样树突状细胞(pDC),从而促进辅助性T细胞1(Th1)和促炎细胞因子的产生以及专业抗原呈递细胞的成熟/活化。这些活性使CpG ODN能够作为免疫佐剂,将抗原特异性免疫反应加速和增强5至500倍。通过保持CpG DNA与免疫原之间的紧密物理接触可优化这些效果。动物攻毒模型证实,将CpG DNA与疫苗共同给药可加速和增强保护性免疫。正在进行的临床研究表明,CpG ODN作为佐剂给人类使用时是安全的且耐受性良好,在某些情况下,它们可增强疫苗诱导的免疫反应。