Klinman D M, Yi A K, Beaucage S L, Conover J, Krieg A M
Section of Retroviral Immunolgy, Division of Viral Products, Food and Drug Administration, Bethesda, MD 20892-4555, USA.
Proc Natl Acad Sci U S A. 1996 Apr 2;93(7):2879-83. doi: 10.1073/pnas.93.7.2879.
Bacterial infection stimulates the host to mount a rapid inflammatory response. A 6-base DNA motif consisting of an unmethylated CpG dinucleotide flanked by two 5' purines and two 3' pyrimidines was shown to contribute to this response by inducing polygonal B-cell activation. This stimulatory motif is 20 times more common in the DNA of bacteria than higher vertebrates. The current work shows that the same motif induces the rapid and coordinated secretion of interleukin (IL) 6, IL-12, and interferon gamma (but not IL-2, IL-3, IL-4, IL-5, or IL-10) in vivo and in vitro. Stimulatory CpG DNA motifs induced B, T, and natural killer cells to secrete cytokine more effectively than did lipopolysaccharide. Thus, immune recognition of bacterial DNA may contribute to the cytokine, as well as the antibody production characteristic of an innate inflammatory response.
细菌感染刺激宿主引发快速的炎症反应。一种由未甲基化的CpG二核苷酸组成的6碱基DNA基序,两侧各有两个5'嘌呤和两个3'嘧啶,已被证明通过诱导多边形B细胞活化来促进这种反应。这种刺激基序在细菌DNA中出现的频率比高等脊椎动物高出20倍。目前的研究表明,相同的基序在体内和体外均可诱导白细胞介素(IL)-6、IL-12和干扰素γ(但不包括IL-2、IL-3、IL-4、IL-5或IL-10)的快速和协同分泌。刺激性CpG DNA基序比脂多糖更有效地诱导B细胞、T细胞和自然杀伤细胞分泌细胞因子。因此,对细菌DNA的免疫识别可能有助于细胞因子的产生,以及先天炎症反应所特有的抗体产生。