Yonezawa H, Kato T, Kuramitsu H K, Okuda K, Ishihara K
Department of Microbiology, Tokyo Dental College, Chiba, Japan.
Oral Microbiol Immunol. 2005 Oct;20(5):259-66. doi: 10.1111/j.1399-302X.2005.00220.x.
We previously demonstrated that a Porphyromonas gingivalis rgpA DNA vaccine induced protective immune responses against P. gingivalis infection in mice. In the present study, reduction in lethality against infection by lethal doses of P. gingivalis was observed in the rgpA DNA vaccine-immunized mice. Cytokine levels in the mouse model with nonlethal doses of infection by P. gingivalis were evaluated to analyze the mechanism of protection by immunization with the rgpA DNA vaccine. After nonlethal challenge with invasive P. gingivalis W50, production of interleukin (IL)-2, IL-4, IL-5 and IL-12 was elevated; however, interferon (IFN)-gamma was lower in the serum of the DNA vaccine-immunized mice than in the serum of nonimmunized mice. The regulation of IFN-gamma production elicited by immunization with the rgpA DNA vaccine may play a significant role in protection against P. gingivalis infection in mice.
我们之前证明,牙龈卟啉单胞菌rgpA DNA疫苗可诱导小鼠产生针对牙龈卟啉单胞菌感染的保护性免疫反应。在本研究中,观察到用rgpA DNA疫苗免疫的小鼠对致死剂量牙龈卟啉单胞菌感染的致死率降低。评估了牙龈卟啉单胞菌非致死剂量感染小鼠模型中的细胞因子水平,以分析用rgpA DNA疫苗免疫的保护机制。在用侵袭性牙龈卟啉单胞菌W50进行非致死性攻击后,白细胞介素(IL)-2、IL-4、IL-5和IL-12的产生增加;然而,DNA疫苗免疫小鼠血清中的干扰素(IFN)-γ低于未免疫小鼠血清中的IFN-γ。用rgpA DNA疫苗免疫引起的IFN-γ产生调节可能在保护小鼠免受牙龈卟啉单胞菌感染中起重要作用。