CPG MOTIFS IN BACTERIAL-DNA TRIGGER DIRECT B-CELL ACTIVATION

被引:2902
作者
KRIEG, AM
YI, AK
MATSON, S
WALDSCHMIDT, TJ
BISHOP, GA
TEASDALE, R
KORETZKY, GA
KLINMAN, DM
机构
[1] UNIV IOWA,COLL MED,DEPT PATHOL,IOWA CITY,IA 52242
[2] UNIV IOWA,COLL MED,DEPT MICROBIOL,IOWA CITY,IA 52242
[3] UNIV IOWA,COLL MED,DEPT PHYSIOL,IOWA CITY,IA 52242
[4] VET AFFAIRS MED CTR,IOWA CITY,IA 52246
[5] US FDA,CTR BIOL EVALUAT & RES,RETROVIRAL IMMUNOL SECT,BETHESDA,MD 20892
关键词
D O I
10.1038/374546a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
UNMETHYLATED CpG dinucleotides are more frequent in the genomes of bacteria and viruses than of vertebrates. We report here that bacterial DNA and synthetic oligodeoxynucleotides containing unmethylated CPG dinucleotides induce murine B cells to proliferate and secrete immunoglobulin in vitro and in vivo. This activation is enhanced by simultaneous signals delivered through the antigen receptor. Optimal B-cell activation requires a DNA motif in which an unmethylated CpG dinucleotide is flanked by two 5' purines and two 3' py,rimidines. Oligodeoxynucleotides containing this CpG motif induce more than 95% of all spleen B cells to enter the cell cycle. These data suggest a possible evolutionary link between immune defence based on the recognition of microbial DNA and the phenomenon of CpG suppression' in vertebrates. The potent immune activation by CpG oligonucleotides has implications for the design and interpretation of studies using 'antisense' oligonucleotides and points to possible new applications as adjuvants.
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页码:546 / 549
页数:4
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