Takahashi I, Nakagawa I, Xu L, Hamada S
Department of Oral Microbiology, Osaka University, Faculty of Dentistry, Japan.
J Periodontal Res. 1996 Nov;31(8):589-95. doi: 10.1111/j.1600-0765.1996.tb00524.x.
The relative roles of alpha beta or gamma delta T cells in protection against Actinobacillus actinomycetemcomitans were analysed by using mutant mice deficient in alpha beta or gamma delta T cell receptor (TCR). The dose of A. actinomycetemcomitans producing lethality for the TCR-alpha deficient mice was 25% of that for control C57BL/6 mice, while that of TCR-delta deficient mice was similar to that of C57BL/6 mice. Reverse transcription (RT)-PCR revealed that gamma delta T cells from the A. actinomycetemcomitans-infected alpha beta TCR deficient mice expressed significant levels of interferon (IFN)-gamma, interleukin (IL)-5 and IL-6 mRNA, whereas alpha beta T cells from A. actinomycetemcomitans-infected gamma delta TCR deficient mice exhibited significant levels of IFN-gamma and IL-2 mRNA. Delayed-type hypersensitivity (DTH) reactions against heat shock protein (HSP) 60 were prominently observed in A. actinomycetemcomitans-infected TCR-delta mutant and C57BL/6 mice, but were absent in TCR-alpha mutant mice, suggesting that the DTH response is exclusively dependent on HSP60-specific alpha beta T cells producing IFN-gamma and IL-2 mRNA. It was found that all the mice used exhibited similar levels of serum IgG and IgM responses against A. actinomycetemcomitans-specific antigens (whole cells and HSP60), suggesting that alpha beta as well as gamma delta T cells participate in the serum immune responses. In addition, the humoral antibody responses displayed in the TCR-alpha deficient mice implies resistance to A. actinomycetemcomitans infection. Thus, the resistance to A. actinomycetemcomitans infection may be ascribed mainly to alpha beta T cells, while gamma delta T cells can partially compensate for the alpha beta T cell defect.
通过使用缺乏αβ或γδT细胞受体(TCR)的突变小鼠,分析了αβ或γδT细胞在抵抗伴放线放线杆菌感染中的相对作用。对TCR-α缺陷小鼠具有致死性的伴放线放线杆菌剂量是对照C57BL/6小鼠的25%,而TCR-δ缺陷小鼠的该剂量与C57BL/6小鼠相似。逆转录(RT)-PCR显示,来自伴放线放线杆菌感染的αβTCR缺陷小鼠的γδT细胞表达显著水平的干扰素(IFN)-γ、白细胞介素(IL)-5和IL-6 mRNA,而来自伴放线放线杆菌感染的γδTCR缺陷小鼠的αβT细胞表现出显著水平的IFN-γ和IL-2 mRNA。在伴放线放线杆菌感染的TCR-δ突变体和C57BL/6小鼠中,对热休克蛋白(HSP)60的迟发型超敏反应(DTH)显著,而在TCR-α突变小鼠中不存在,这表明DTH反应完全依赖于产生IFN-γ和IL-2 mRNA的HSP60特异性αβT细胞。发现所有使用的小鼠对伴放线放线杆菌特异性抗原(全细胞和HSP60)表现出相似水平的血清IgG和IgM反应,这表明αβ以及γδT细胞参与血清免疫反应。此外,TCR-α缺陷小鼠中显示的体液抗体反应意味着对伴放线放线杆菌感染具有抗性。因此,对伴放线放线杆菌感染的抗性可能主要归因于αβT细胞,而γδT细胞可以部分补偿αβT细胞缺陷。