Immune mechanisms and therapeutic potential of CpG oligodeoxynucleotides

被引:59
作者
Wilson, Heather L. [1 ]
Dar, Arshud [1 ]
Napper, Scott K. [1 ]
Lopez, A. Marianela [1 ]
Babiuk, Lorne A. [1 ]
Mutwiri, George K. [1 ]
机构
[1] Univ Saskatchewan, Vaccine & Infect Dis Org, Saskatoon, SK, Canada
关键词
CpG oligodeoxynucleotides; immunoprotection; immunotherapy; innate immunity; toll-like receptor 9;
D O I
10.1080/08830180600785868
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Unmethylated CpG motifs in bacterial DNA and synthetic oligodeoxynucleotidesactivate immune cells that express Toll-like Receptor 9. Activation through this receptor triggers cellular signaling that leads to production of a proinflammatory and a Thl-type, antigen-specific immune response. The immunostimulatory effects of CpG oligodeoxynucleotides confer protection against infectious disease, allergy and cancer in animal models, and clinical trials have been initiated. However, CpG oligodeoxynucleotides may exacerbate disease in some situations. We will review current concepts in the mechanisms of activating Toll-like Receptor 9 with CpG oligodeoxynucleotides and highlight opportunities for using large animal models to better determine the mechanisms of action.
引用
收藏
页码:183 / 213
页数:31
相关论文
共 168 条
[41]   A distal regulatory region is required for constitutive and IFN-β-induced expression of murine TLR9 gene [J].
Guo, Z ;
Garg, S ;
Hill, KM ;
Jayashankar, L ;
Mooney, MR ;
Hoelscher, M ;
Katz, JM ;
Boss, JM ;
Sambhara, S .
JOURNAL OF IMMUNOLOGY, 2005, 175 (11) :7407-7418
[42]  
Gürsel M, 2002, J LEUKOCYTE BIOL, V71, P813
[43]   CpG-DNA-specific activation of antigen-presenting cells requires stress kinase activity and is preceded by non-specific endocytosis and endosomal maturation [J].
Häcker, H ;
Mischak, H ;
Miethke, T ;
Liptay, S ;
Schmid, R ;
Sparwasser, T ;
Heeg, K ;
Lipford, GB ;
Wagner, H .
EMBO JOURNAL, 1998, 17 (21) :6230-6240
[44]   The poxvirus protein A52R targets toll-like receptor signaling complexes to suppress host defense [J].
Harte, MT ;
Haga, IR ;
Maloney, G ;
Gray, P ;
Reading, PC ;
Bartlett, NW ;
Smith, GL ;
Bowie, A ;
O'Neill, LAJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (03) :343-351
[45]   CpG DNA: A potent signal for growth, activation, and maturation of human dendritic cells [J].
Hartmann, G ;
Weiner, GJ ;
Krieg, AM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (16) :9305-9310
[46]   Mechanism and function of a newly identified CpG DNA moth in human primary B cells [J].
Hartmann, G ;
Krieg, AM .
JOURNAL OF IMMUNOLOGY, 2000, 164 (02) :944-952
[47]   CpG DNA and LPS induce distinct patterns of activation in human monocytes [J].
Hartmann, G ;
Krieg, AM .
GENE THERAPY, 1999, 6 (05) :893-903
[48]   Synthetic CpG oligodeoxynucleotides accelerate the development of lupus nephritis during preactive phase in NZB x NZWF1 mice [J].
Hasegawa, K ;
Hayashi, T .
LUPUS, 2003, 12 (11) :838-845
[49]   THE TOLL GENE OF DROSOPHILA, REQUIRED FOR DORSAL-VENTRAL EMBRYONIC POLARITY, APPEARS TO ENCODE A TRANSMEMBRANE PROTEIN [J].
HASHIMOTO, C ;
HUDSON, KL ;
ANDERSON, KV .
CELL, 1988, 52 (02) :269-279
[50]   Inhibition of experimental asthma by indoleamine 2,3-dioxygenase [J].
Hayashi, T ;
Beck, L ;
Rossetto, C ;
Gong, X ;
Takikawa, O ;
Takabayashi, K ;
Broide, DH ;
Carson, DA ;
Raz, E .
JOURNAL OF CLINICAL INVESTIGATION, 2004, 114 (02) :270-279