Johnson Lawrence L, Lanthier Paula, Hoffman Jessica, Chen Wangxue
Trudeau Institute, Inc., Saranac Lake, NY 12983, USA.
Vaccine. 2004 Sep 28;22(29-30):4054-61. doi: 10.1016/j.vaccine.2004.03.056.
Prior studies have demonstrated that B cells are important components of protection in vaccinated mice challenged intraperitoneally with a highly virulent type I strain of Toxoplasma gondii parasites. However, it is not known whether B cells are required for vaccinated mice to successfully resist a more physiologically relevant challenge infection with a mildly virulent type II strain of T. gondii. To investigate that question, we vaccinated B cell-deficient C57BL/6 (microMT) mice with an attenuated strain of T. gondii and challenged them with a potentially lethal oral dose of type II T. gondii cysts. Vaccinated microMT mice survived the challenge as well as vaccinated B6 controls, controlled parasites equally well in critical tissues, produced equivalent levels of mRNA for several type 1 cytokines, and exhibited comparably mild histopathology. Thus, a vaccine can protect against infection with a mildly virulent type II strain of T. gondii in the absence of a B cell-dependent immune response.
先前的研究表明,在经腹腔接种高毒力I型弓形虫寄生虫进行攻击的疫苗接种小鼠中,B细胞是保护性免疫的重要组成部分。然而,尚不清楚B细胞对于疫苗接种小鼠成功抵抗更具生理相关性的温和毒力II型弓形虫攻击感染是否必需。为了研究这个问题,我们用减毒的弓形虫菌株对B细胞缺陷的C57BL/6(microMT)小鼠进行疫苗接种,并用可能致死剂量的II型弓形虫囊肿经口攻击它们。接种疫苗的microMT小鼠与接种疫苗的B6对照小鼠一样在攻击中存活下来,在关键组织中同样有效地控制了寄生虫,产生了几种1型细胞因子的等效mRNA水平,并且表现出相当轻微的组织病理学变化。因此,在没有B细胞依赖性免疫反应的情况下,疫苗可以预防温和毒力II型弓形虫的感染。