3.8 Article

Phosphate-modified CpG oligonucleotides induce in vitro maturation of human myeloid dendritic cells

期刊

VAVILOVSKII ZHURNAL GENETIKI I SELEKTSII
卷 24, 期 6, 页码 653-660

出版社

RUSSIAN ACAD SCI, INST CYTOLOGY GENETICS
DOI: 10.18699/VJ20.659

关键词

monocytes; dendritic cells; differentiation; maturation; PAMP- and DAMP-activators; allo-MLR; CpG-oligo-nucleotide

资金

  1. Russian Foundation for Basic Research [18-29-09045_mk]
  2. Ministry of Science and Higher Education of the Russian Federation [FSUS-2020-0035]

向作者/读者索取更多资源

Myeloid dendritic cells (DCs) play an important role in the immune response; therefore, the search for compounds that can effectively activate DCs is a needful goal. This study was aimed to investigate the effect of synthetic CpG oligodeoxynucleotides (CpG-ODN) on the maturation and allostimulatory activity of myeloid DCs in comparison with other PAMP and DAMP molecules. For the research, we synthesized known CpG-ODN class C (SD-101 and D-SL03) containing thiophosphate internucleotide groups, and their original phosphate-modified analogues (SD-101M and D-SLO3M) with mesylphosphoramide internucleotide groups (M = p-modification).The effects of CpG-ODN and other activators were evaluated on DCs generated from blood monocytes in the presence of GM-CSF and IFN-alpha (IFN-DC) or IL-4 (IL4-DC). Evaluation of the intracellular TLR-9 expression showed that both types of DCs (IFN-DC and IL4-DC) contained on average 52 and 80 % of TLR-9-positive cells, respectively. The CpG-ODNs studied enhanced the allostimulatory activity of IFN-DCs, and the effect of mu-modified CpG-ODNs was higher than that of CpG-ODNs with thiophosphate groups. The stimulating effect of CpG-ODN at a dose of 1.0 mu g/ml was comparable (for D-SL03, D-SLO3M, SD-101) with or exceeded (for SD-101M) the effect of LPS at a dose of 10 mu g/ml. At the same time, IFN-DCs were characterized by greater sensitivity to the action of CpG-ODNs than IL4-DCs. The enhancement of DC allostimulatory activity in the presence of CpG-ODNs was associated with the induction of final DC maturation, which was confirmed by a significant decrease in the number of CD14+DC, an increase in mature CD831DC and a trend towards an increase in CD86+DC. Interestingly, the characteristic ability of LPS to enhance the expression of the co-stimulatory molecule OX4OL on DCs was revealed only for the p-analogue SD-101M. In addition, CpG-ODNs (SD-101 and SD-101M) had a stimulatory effect on IFN-gamma production comparable to the action of LPS. The data obtained indicate a stimulating effect of CpG-ODN on the maturation and allostimulatory activity of human myeloid DCs, which is more pronounced for p-modified analogs.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

3.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据