Taubman Martin A, Han Xiaozhe, Larosa Karen B, Socransky Sigmund S, Smith Daniel J
Department of Immunology, The Forsyth Institute, 140 The Fenway, Boston, MA 02115-3799, USA.
Infect Immun. 2007 Aug;75(8):4088-96. doi: 10.1128/IAI.00623-07. Epub 2007 May 21.
Certain CpG motifs found in bacterial DNA enhance immune responses through Toll-like receptor 9 (TLR-9) and may also demonstrate adjuvant properties. Our objective was to determine if DNA from bacteria associated with periodontal disease could affect the immune response to other bacterial antigens in the oral cavity. Streptococcus sobrinus glucosyltransferase (GTF), an enzyme involved in dental caries pathogenesis, was used as a test antigen. Rowett rats were injected with aluminum hydroxide (alum) with buffer, alum-GTF, or alum-GTF together with either Escherichia coli DNA, Fusobacterium nucleatum DNA, or Porphyromonas gingivalis DNA. Contrary to expectation, animals receiving alum-GTF plus bacterial DNA (P. gingivalis in particular) demonstrated significantly reduced serum immunoglobulin G (IgG) antibody, salivary IgA antibody, and T-cell proliferation to GTF compared to animals immunized with alum-GTF alone. A diminished antibody response was also observed after administration of alum-GTF with the P. gingivalis DNA either together or separately, indicating that physical complexing of antigen and DNA was not responsible for the reduction in antibody. Since TLR triggering by DNA induces synthesis of prospective suppressive factors (e.g., suppressor of cytokine signaling [SOCS]), the effects of P. gingivalis DNA and GTF exposure on rat splenocyte production of SOCS family molecules and inflammatory cytokines were investigated in vitro. P. gingivalis DNA significantly up-regulated SOCS1 and SOCS5 expression and down-regulated interleukin-10 expression by cultured splenocytes. These results suggested that DNA from periodontal disease-associated bacteria did not enhance, but in fact suppressed, the immune response to a protein antigen from cariogenic streptococci, potentially through suppressive SOCS components triggered by innate mechanisms.
在细菌DNA中发现的某些CpG基序可通过Toll样受体9(TLR-9)增强免疫反应,并且可能还具有佐剂特性。我们的目的是确定来自与牙周疾病相关细菌的DNA是否会影响对口腔中其他细菌抗原的免疫反应。变形链球菌葡糖基转移酶(GTF)是一种参与龋齿发病机制的酶,用作测试抗原。将罗威特大鼠注射氢氧化铝(明矾)加缓冲液、明矾-GTF,或明矾-GTF与大肠杆菌DNA、具核梭杆菌DNA或牙龈卟啉单胞菌DNA一起注射。与预期相反,与单独用明矾-GTF免疫的动物相比,接受明矾-GTF加细菌DNA(特别是牙龈卟啉单胞菌DNA)的动物对GTF的血清免疫球蛋白G(IgG)抗体、唾液IgA抗体和T细胞增殖显著降低。在同时或分别给予明矾-GTF和牙龈卟啉单胞菌DNA后也观察到抗体反应减弱,这表明抗原与DNA的物理复合不是抗体减少的原因。由于DNA触发TLR会诱导潜在抑制因子的合成(例如,细胞因子信号传导抑制因子[SOCS]),因此在体外研究了牙龈卟啉单胞菌DNA和GTF暴露对大鼠脾细胞SOCS家族分子和炎性细胞因子产生的影响。牙龈卟啉单胞菌DNA显著上调培养的脾细胞中SOCS1和SOCS5的表达,并下调白细胞介素-10的表达。这些结果表明,来自与牙周疾病相关细菌的DNA并未增强,而是实际上抑制了对致龋链球菌蛋白质抗原的免疫反应,这可能是通过先天机制触发的抑制性SOCS成分实现的。