Prophylactic vaccines mimic synthetic CpG oligonucleotides in their ability to modulate immune responses

被引:22
作者
de Vries, I. Jolanda M. [1 ,2 ,3 ]
Tel, Jurjen [1 ]
Benitez-Ribas, Daniel [1 ]
Torensma, Ruurd [1 ]
Figdor, Carl G. [1 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Tumor Immunol, Nijmegen Ctr Mol Life Sci, NL-6500 HB Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Med Ctr, Dept Med Oncol, Nijmegen Ctr Mol Life Sci, NL-6500 HB Nijmegen, Netherlands
[3] Radboud Univ Nijmegen, Med Ctr, Dept Pediat Hematooncol, Nijmegen Ctr Mol Life Sci, NL-6500 HB Nijmegen, Netherlands
关键词
CpG oligonucleotides; Vaccines; Plasmacytoid dendritic cells; TOLL receptors; Immune response; PLASMACYTOID DENDRITIC CELLS; TOLL-LIKE RECEPTORS; INNATE IMMUNITY; TLR9; AGONISTS; ACTIVATION; DNA; TOLL-LIKE-RECEPTOR-9; PROTEINS; SUBSETS; MOTIFS;
D O I
10.1016/j.molimm.2010.12.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Synthetic oligonucleotide ligands that bind to toll-like receptors are known to modulate the immune response via the activation of antigen presenting cells, and were therefore proposed as a novel form of vaccine adjuvant. Clinical-grade they are, however, not readily available. Here, we show that commonly used prophylactic vaccines for infectious diseases like measles, mumps and tuberculosis exhibit the same immune modulating behavior as synthetic CpG oligonucleotides in terms of their ability to stimulate IFN-alpha production and plasmacytoid dendritic cell maturation. Featuring the additional advantages of low-cost and proven safety, these vaccines could therefore be attractive alternatives to CpG oligonucleotides as adjuvants for immunotherapy. This previously undiscovered characteristic of prophylactic vaccines also sheds new light on the mechanisms by which they operate and is extremely interesting for vaccine development. Moreover, the finding that prophylactic vaccines trigger TLRs like synthetic oligonucleotides opens the possibility to predict the immune response of new vaccines. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:810 / 817
页数:8
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