Onyilagha Chukwunonso, Singh Rani, Gounni Abdelilah Soussi, Uzonna Jude Ezeh
Faculty of Health Sciences, Department of Immunology, College of Medicine, University of Manitoba, Winnipeg, MB, Canada.
Faculty of Health Sciences, Department of Medical Microbiology, College of Medicine, University of Manitoba, Winnipeg, MB, Canada.
Front Immunol. 2017 Jul 14;8:803. doi: 10.3389/fimmu.2017.00803. eCollection 2017.
African trypanosomiasis (sleeping sickness) poses serious threat to human and animal health in sub-Saharan Africa. Because there is currently no vaccine for preventing this disease and available drugs are not safe, understanding the mechanisms that regulate resistance and/or susceptibility to the disease could reveal novel targets for effective disease therapy and prevention. Thymic stromal lymphopoietin (TSLP) plays a critical role in driving Th2 immune response. Although susceptibility to experimental infection in mice is associated with excessive proinflammatory responses due in part to impaired Th2 response, the role of TSLP in resistance to African trypanosomiasis has not been well studied. Here, we investigated whether TSLP is critical for maintaining Th2 environment necessary for survival of -infected mice. We observed an increased TSLP level in mice after infection with , suggesting a role for this cytokine in resistance to the infection. Indeed, TSLPR mice were more susceptible to infection and died significantly earlier than their wild-type (WT) controls. Interestingly, serum levels of IFN-γ and TNF-α and the frequency of IFN-γ- and TNF-α-producing CD4 T cells in the spleens and liver were significantly higher in infected TSLPR mice than in the WT control mice. Susceptibility was also associated with excessive M1 macrophage activation. Treatment of TSLPR mice with anti-IFN-γ mAb during infection abolished their enhanced susceptibility to infection. Collectively, our study shows that TSLP plays a critical role in resistance to infection by dampening the production of proinflammatory cytokines and its associated M1 macrophage activation.
非洲锥虫病(昏睡病)对撒哈拉以南非洲地区的人类和动物健康构成严重威胁。由于目前尚无预防该疾病的疫苗,且现有药物不安全,了解调节对该疾病抗性和/或易感性的机制可能会揭示有效的疾病治疗和预防的新靶点。胸腺基质淋巴细胞生成素(TSLP)在驱动Th2免疫反应中起关键作用。尽管小鼠对实验性感染的易感性与部分由于Th2反应受损导致的过度促炎反应有关,但TSLP在抵抗非洲锥虫病中的作用尚未得到充分研究。在这里,我们研究了TSLP对于维持感染小鼠生存所必需的Th2环境是否至关重要。我们观察到感染后小鼠体内TSLP水平升高,表明这种细胞因子在抵抗感染中发挥作用。事实上,TSLPR小鼠比野生型(WT)对照更易感染,并明显更早死亡。有趣的是,感染的TSLPR小鼠脾脏和肝脏中IFN-γ和TNF-α的血清水平以及产生IFN-γ和TNF-α的CD4 T细胞频率显著高于WT对照小鼠。易感性还与过度的M1巨噬细胞活化有关。感染期间用抗IFN-γ单克隆抗体治疗TSLPR小鼠消除了它们对感染的易感性增强。总体而言,我们的研究表明,TSLP通过抑制促炎细胞因子的产生及其相关的M1巨噬细胞活化,在抵抗感染中起关键作用。