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多CpG基序对HIV-1 DNA疫苗的佐剂作用。

Adjuvant effect of multi-CpG motifs on an HIV-1 DNA vaccine.

作者信息

Kojima Yoshitsugu, Xin Ke-Qin, Ooki Takaaki, Hamajima Kenji, Oikawa Tomohiro, Shinoda Kaori, Ozaki Tomomi, Hoshino Yuka, Jounai Nao, Nakazawa Masatoshi, Klinman Dennis, Okuda Kenji

机构信息

Department of Bacteriology, University School of Medicine, Yokohama City, Yokohama 236-0004, Japan.

出版信息

Vaccine. 2002 Jul 26;20(23-24):2857-65. doi: 10.1016/s0264-410x(02)00238-4.

Abstract

Synthetic oligodeoxynucleotides (ODN) containing unmethylated CpG motifs trigger an immune response characterized by the activation of B cells, NK cells and monocytes/macrophages. Based on evidence that the immunogenicity of DNA vaccines can be augmented by the addition of CpG motifs, 5-20 additional CpG motifs were cloned into a pUC-derived plasmid. Treating bone-marrow derived dendritic cells (BM-DCs) with CpG-enriched plasmids in vitro boosted their expressions of MHC class II molecules, the CD40 and CD86 activation markers. Co-administering the CpG-enriched plasmids with a DNA vaccine encoding the envelope glycoprotein of HIV to BALB/c mice significantly increased HIV-specific cell mediated and humoral immunity. A significant boost was observed when the CpG plasmid was administered either 2 or 4 days after DNA vaccination. Plasmids containing 20 CpG copies were the most effective immune enhancers both in vitro and in vivo. These results suggest that plasmids containing multiple CpG motifs may improve the immunogenicity of DNA vaccines.

摘要

含有未甲基化CpG基序的合成寡脱氧核苷酸(ODN)可引发一种免疫反应,其特征为B细胞、自然杀伤细胞和单核细胞/巨噬细胞的激活。基于DNA疫苗的免疫原性可通过添加CpG基序得以增强这一证据,将5 - 20个额外的CpG基序克隆到一个源自pUC的质粒中。体外使用富含CpG的质粒处理骨髓来源的树突状细胞(BM - DC)可提高其MHC II类分子、CD40和CD86激活标志物的表达。将富含CpG的质粒与编码HIV包膜糖蛋白的DNA疫苗共同给予BALB/c小鼠,可显著增强HIV特异性细胞介导免疫和体液免疫。在DNA疫苗接种后2天或4天给予CpG质粒时,观察到显著增强效果。含有20个CpG拷贝的质粒在体外和体内都是最有效的免疫增强剂。这些结果表明,含有多个CpG基序的质粒可能会提高DNA疫苗的免疫原性。

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