Shibui Akiko, Hozumi Nobumichi, Shiraishi Chiharu, Sato Yoshitaka, Iida Hajime, Sugano Sumio, Watanabe Junichi
Research Institute for Biological Sciences, Tokyo University of Science, Chiba, Japan.
Parasitol Res. 2009 Jul;105(1):281-6. doi: 10.1007/s00436-009-1435-8. Epub 2009 Apr 8.
Plasmodium berghei ANKA causes lethal malaria in mice. It is well established that C57BL/6 mice die early with fulminant symptoms including convulsion, whereas BALB/c mice survive this phase and die later of anemia and prostration. Early death in C57BL/6 mice has been considered to result from the adverse effects of inflammatory cytokines. To elucidate the CD4(+) T cell responses in early death due to severe malaria, the kinetics of CD4(+) T cells were compared by analyzing cell surface markers and the production of cytokines and transcription factors. The results revealed that cytokine production by CD4(+) T cells was induced as early as 5 days after infection and the maintenance of higher levels of IL-4 and IL-10 may be associated with the protection of BALB/c mice from early death. These results suggest that parasite control in the early phase of infection may be important for the development of an effective vaccine.
伯氏疟原虫ANKA株可在小鼠中引发致死性疟疾。众所周知,C57BL/6小鼠会早期死亡,伴有惊厥等暴发性症状,而BALB/c小鼠在此阶段存活下来,随后死于贫血和虚脱。C57BL/6小鼠的早期死亡被认为是由炎性细胞因子的不良反应所致。为阐明重症疟疾早期死亡中的CD4(+) T细胞反应,通过分析细胞表面标志物以及细胞因子和转录因子的产生情况,对CD4(+) T细胞的动力学进行了比较。结果显示,感染后5天CD4(+) T细胞就开始产生细胞因子,较高水平的IL-4和IL-10的维持可能与保护BALB/c小鼠免于早期死亡有关。这些结果表明,感染早期对寄生虫的控制对于开发有效的疫苗可能很重要。