CpG motifs in bacterial DNA and their immune effects

被引:2093
作者
Krieg, AM [1 ]
机构
[1] Dept Vet Affairs Med Ctr, Iowa City, IA 52246 USA
[2] Univ Iowa, Coll Med, Dept Internal Med, Iowa City, IA 52242 USA
[3] Coley Pharmaceut Grp, Wellesley, MA 02481 USA
关键词
D O I
10.1146/annurev.immunol.20.100301.064842
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 are prevalent in bacterial but not vertebrate genomic DNAs. Oligodeoxynucleotides (ODN) containing CpG motifs activate host defense mechanisms leading to innate and acquired immune responses. The recognition of CpG motifs requires Toll-like receptor (TLR) 9, which triggers alterations in cellular redox balance and the induction of cell signaling pathways including the mitogen activated protein kinases (MAPKs) and NFkappaB. Cells that express TLR-9, which include plasmacytoid dendritic cells (PDCs) and B cells, produce Th1-like proinflammatory cytokines, interferons, and chemokines. Certain CpG motifs (CpG-A) are especially potent at activating NK cells and inducing IFN-alpha production by PDCs, while other motifs (CpG-B) are especially potent B cell activators. CpG-induced activation of innate immunity protects against lethal challenge with a wide variety of pathogens, and has therapeutic activity in murine models of cancer and allergy. CpG ODN also enhance the development of acquired immune responses for prophylactic and therapeutic vaccination.
引用
收藏
页码:709 / 760
页数:52
相关论文
共 314 条
[11]   The effects of DNA containing CpG motif on dendritic cells [J].
Behboudi, S ;
Chao, D ;
Klenerman, P ;
Austyn, J .
IMMUNOLOGY, 2000, 99 (03) :361-366
[12]   BINDING, UPTAKE, AND INTRACELLULAR TRAFFICKING OF PHOSPHOROTHIOATE-MODIFIED OLIGODEOXYNUCLEOTIDES [J].
BELTINGER, C ;
SARAGOVI, HU ;
SMITH, RM ;
LESAUTEUR, L ;
SHAH, N ;
DEDIONISIO, L ;
CHRISTENSEN, L ;
RAIBLE, A ;
JARETT, L ;
GEWIRTZ, AM .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (04) :1814-1823
[13]  
Bendigs S, 1999, EUR J IMMUNOL, V29, P1209, DOI 10.1002/(SICI)1521-4141(199904)29:04<1209::AID-IMMU1209>3.0.CO
[14]  
2-J
[15]   CPG ISLANDS AS GENE MARKERS IN THE VERTEBRATE NUCLEUS [J].
BIRD, AP .
TRENDS IN GENETICS, 1987, 3 (12) :342-347
[16]   Biochemistry of antigen receptor signaling in mature and developing B lymphocytes [J].
Birkeland, ML ;
Monroe, JG .
CRITICAL REVIEWS IN IMMUNOLOGY, 1997, 17 (3-4) :353-385
[17]  
Biswas S, 1999, CURR SCI INDIA, V76, P1012
[18]   Synthetic unmethylated cytosine-phosphate-guanosine oligodeoxynucleotides are potent stimulators of antileukemia responses in naive and bone marrow transplant recipients [J].
Blazar, BR ;
Krieg, AM ;
Taylor, PA .
BLOOD, 2001, 98 (04) :1217-1225
[19]   Non-coding plasmid DNA induces IFN-γ in vivo and suppresses autoimmune encephalomyelitis [J].
Boccaccio, GL ;
Mor, F ;
Steinman, L .
INTERNATIONAL IMMUNOLOGY, 1999, 11 (02) :289-296
[20]   Characterization and modulation of immune stimulation by modified oligonucleotides [J].
Boggs, RT ;
McGraw, K ;
Condon, T ;
Flournoy, S ;
Villiet, P ;
Bennett, CF ;
Monia, BP .
ANTISENSE & NUCLEIC ACID DRUG DEVELOPMENT, 1997, 7 (05) :461-471