Tokoro Y, Matsuki Y, Yamamoto T, Suzuki T, Hara K
Department of Periodontology, Niigata University School of Dentistry, Japan.
Clin Exp Immunol. 1997 Jan;107(1):166-74. doi: 10.1046/j.1365-2249.1997.d01-880.x.
It has been suggested that the types of inflammatory round cell infiltrates and the divergence in the cytokine production profile by macrophages and helper T cells regulate the course of infectious or inflammatory diseases, including periodontitis and gingivitis. We examined the expression of IL-1alpha, IL-1beta, IL-2, IL-4, IL-5, IL-6 and tumour necrosis factor-alpha (TNF-alpha) mRNA in the inflamed gingiva by in situ hybridization. The results of single-cell analysis were used as data sets for statistical analyses. The density of cells expressing IL-1alpha, IL-4 and IL-5 mRNA was higher in periodontitis than in gingivitis. IL-2 mRNA-expressing cells were almost absent in gingivitis specimens. Principal component analysis disclosed three factors explaining 84.8% of the variance: one accounting for 40.5% of the variance and mainly regulated by IL-1alpha, IL-1beta, IL-6 and TNF-alpha, and two others, explaining 29.9% and 14.4% of the variance, describing the relationship between the types of cytokines derived from macrophages or Th2 type. These results suggest that the cytokines produced by inflammatory cells infiltrating in the gingival tissue are influential on the progression of gingivitis, an acute and reversible inflammatory condition, to chronic and destructive periodontitis. Thus, periodontal disease progression may be regulated by the local cytokine network, and the bias in this network towards a Th2-type cytokine dominance could be an exacerbating factor.
有人提出,炎症性圆形细胞浸润的类型以及巨噬细胞和辅助性T细胞细胞因子产生谱的差异会调节包括牙周炎和牙龈炎在内的感染性或炎症性疾病的进程。我们通过原位杂交检测了炎症牙龈中白细胞介素-1α(IL-1α)、白细胞介素-1β(IL-1β)、白细胞介素-2(IL-2)、白细胞介素-4(IL-4)、白细胞介素-5(IL-5)、白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)mRNA的表达。单细胞分析的结果用作统计分析的数据集。牙周炎中表达IL-1α、IL-4和IL-5 mRNA的细胞密度高于牙龈炎。在牙龈炎标本中几乎不存在表达IL-2 mRNA的细胞。主成分分析揭示了三个解释84.8%方差的因素:一个占方差的40.5%,主要受IL-1α、IL-1β、IL-6和TNF-α调节,另外两个分别解释29.9%和14.4%的方差,描述了巨噬细胞或Th2型衍生的细胞因子类型之间的关系。这些结果表明,浸润在牙龈组织中的炎症细胞产生的细胞因子对牙龈炎(一种急性且可逆的炎症状态)向慢性和破坏性牙周炎的进展有影响。因此,牙周疾病的进展可能受局部细胞因子网络调节,并且该网络向Th2型细胞因子优势的偏差可能是一个加剧因素。