Roy Chad J, Warfield Kelly L, Welcher Brent C, Gonzales Raoul F, Larsen Tom, Hanson Julie, David Chella S, Krakauer Theresa, Bavari Sina
U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, MD 21702, USA.
Infect Immun. 2005 Apr;73(4):2452-60. doi: 10.1128/IAI.73.4.2452-2460.2005.
Staphylococcal enterotoxins (SEs) belong to a large group of bacterial exotoxins that cause severe immunopathologies, especially when delivered as an aerosol. SEs elicit the release of lethal amounts of cytokines by binding to major histocompatibility complex (MHC) class II and cross-linking susceptible T-cell receptors. Efforts to develop effective therapeutic strategies to protect against SEs delivered as an aerosol have been hampered by the lack of small animal models that consistently emulate human responses to these toxins. Here, we report that human leukocyte antigen-DQ8 (HLA-DQ8) transgenic (Tg) mice, but not littermate controls, succumbed to lethal shock induced by SEB aerosols without potentiation. Substantial amounts of perivascular edema and inflammatory infiltrates were noted in the lungs of Tg mice, similar to the pathology observed in nonhuman primates exposed by aerosol to SEB. Furthermore, the observed pathologies and lethal shock correlated with an upsurge in proinflammatory cytokine mRNA gene expression in the lungs and spleens, as well as with marked increases in the levels of proinflammatory circulating cytokines in the Tg mice. Unlike the case for littermate controls, telemetric evaluation showed significant hypothermia in Tg mice exposed to lethal doses of SEB. Taken together, these results show that this murine model will allow for the examination of therapeutics and vaccines developed specifically against SEB aerosol exposure and possibly other bacterial superantigens in the context of human MHC class II receptors.
葡萄球菌肠毒素(SEs)属于一大类细菌外毒素,可引发严重的免疫病理反应,尤其是以气溶胶形式传播时。SEs通过与主要组织相容性复合体(MHC)II类分子结合并交联易感T细胞受体,引发致死量细胞因子的释放。由于缺乏能够始终如一地模拟人类对这些毒素反应的小动物模型,开发针对气溶胶形式SEs的有效治疗策略的努力受到了阻碍。在此,我们报告人类白细胞抗原-DQ8(HLA-DQ8)转基因(Tg)小鼠而非同窝对照小鼠,在无增强作用的情况下死于SEB气溶胶诱导的致死性休克。在Tg小鼠的肺中观察到大量血管周围水肿和炎性浸润,类似于气溶胶暴露于SEB的非人灵长类动物中观察到的病理变化。此外,观察到的病理变化和致死性休克与肺和脾脏中促炎细胞因子mRNA基因表达的激增相关,也与Tg小鼠循环促炎细胞因子水平的显著升高相关。与同窝对照不同,遥测评估显示暴露于致死剂量SEB的Tg小鼠出现明显体温过低。综上所述,这些结果表明,该小鼠模型将有助于研究专门针对SEB气溶胶暴露以及可能针对人类MHC II类受体背景下其他细菌超抗原开发的治疗方法和疫苗。