Toxoplasmosis Laboratory, Operational Direction Communicable and Infectious Diseases, Scientific Institute of Public Health, Site Uccle, 642 rue Engeland, 1180 Brussels, Belgium.
Microbes Infect. 2011 Apr;13(4):394-404. doi: 10.1016/j.micinf.2011.01.006. Epub 2011 Jan 22.
CD4(+)CD25(+)Foxp3(+) T regulatory (Treg) cells, are known to regulate responses to infectious agents. Here we compared disease progression in BALB/c and C57BL/6(B6) mice infected perorally with Toxoplasma gondii for 7 days and examined the affect of partial depletion of Treg cells in these mice. BALB/c mice were seen to be resistant to peroral infection whereas B6 mice were susceptible in terms of mortality. Although the depletion of Treg cells before infection had no effect on the survival of B6 or BALB/c mice, it resulted in increased parasite burdens in BALB/c mice, especially in the lamina propria, but not in B6 mice. Pro-inflammatory cytokines were also increased in Treg cells depleted BALB/c mice as compared to B6 mice. In addition Treg cell depleted BALB/c mice displayed increased ileal histopathology compared to their non-treated counterparts. These findings provide evidence for the contribution of Treg cells, in the resistance of BALB/c mice against peroral T. gondii infection.
CD4(+)CD25(+)Foxp3(+)T 调节性 (Treg) 细胞,已知可调节对感染因子的反应。在这里,我们比较了 BALB/c 和 C57BL/6(B6) 小鼠经口感染弓形虫 7 天后的疾病进展,并研究了在这些小鼠中部分耗尽 Treg 细胞的影响。BALB/c 小鼠对经口感染具有抗性,而 B6 小鼠则在死亡率方面易感。尽管在感染前耗尽 Treg 细胞对 B6 或 BALB/c 小鼠的存活没有影响,但它导致 BALB/c 小鼠中的寄生虫负担增加,特别是在固有层,但在 B6 小鼠中没有。与 B6 小鼠相比,Treg 细胞耗尽的 BALB/c 小鼠中的促炎细胞因子也增加了。此外,与未治疗的对照相比,Treg 细胞耗尽的 BALB/c 小鼠显示出回肠组织病理学增加。这些发现为 Treg 细胞在 BALB/c 小鼠抵抗经口 T. gondii 感染中的作用提供了证据。