Approaches to enhancing immune responses stimulated by CpG oligodeoxynucleotides

被引:53
作者
Mutwiri, George [1 ]
Littel-van den Hurk, Sylvia van Drunen [1 ]
Babiuk, Lorne A. [1 ,2 ]
机构
[1] Univ Saskatchewan, Vaccine & Infect Dis Org Int Vaccine Ctr, Saskatoon, SK S7N 5E3, Canada
[2] Univ Alberta, Edmonton, AB T6G 2J9, Canada
基金
美国国家卫生研究院; 加拿大自然科学与工程研究理事会;
关键词
CpG DNA; Oligodeoxynucleotides; Toll-like receptors; Polyphosphazenes; Formulation; Delivery; RESPIRATORY SYNCYTIAL VIRUS; REGULATORY T-CELLS; SALMONELLA-ENTERITIDIS INFECTION; ANTIGEN-PRESENTING CELL; B SURFACE-ANTIGEN; DENDRITIC CELLS; MUCOSAL IMMUNIZATION; IN-VIVO; INTRANASAL IMMUNIZATION; ALUMINUM-HYDROXIDE;
D O I
10.1016/j.addr.2008.12.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
CpG oligodeoxynucleotides (ODN) activate the immune system and are promising immunotherapeutic agents against infectious diseases, allergy/asthma and cancer. It has become apparent that while CpG ODN are potent immune activators in mice, their immune stimulatory effects are often less dramatic in humans and large animals. This disparity between rodents and mammals has been attributed to the differences in TLR9 expression in different species. This along with the sometimes transient activity of ODN may limit its potential immunotherapeutic applications. Several approaches to enhance the activity of CpG ODN have been explored including formulation of ODN in depot-forming adjuvants, and more recently, coadministration with polyphosphazenes, inhibitors of cytokines that downregulate TLR9 activation, and simultaneous activation with multiple TLR agonists. We will discuss these approaches and the mechanisms involved, with emphasis on what we have learned from large animal models. (c) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:226 / 232
页数:7
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