Miller Renee, Wen Xiangshu, Dunford Bradley, Wang Xisheng, Suzuki Yasuhiro
Center for Molecular Medicine and Infectious Diseases, Department of Biomedical Sciences and Pathobiology, Virginia-Maryland Regional College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA.
J Interferon Cytokine Res. 2006 Nov;26(11):787-92. doi: 10.1089/jir.2006.26.787.
To examine whether cytokine production of CD4(+)immune T cells and CD8(+)immune T cells in Toxoplasma gondii-infected mice differ in their responses to infected cells and to soluble antigens of the parasite, we compared the production of interferon-gamma (IFN-gamma), interleukin-2 (IL-2), IL-4, and IL-10 by the immune T cell populations following in vitro stimulation with tachyzoite-infected macrophages and tachyzoite lysate antigens (TLA). Both CD4(+)and CD8(+)immune T cells produced large amounts of IFN-gamma in response to either infected macrophages or TLA, but the CD4(+)T cells produced greater amounts of the cytokine than did the CD8(+)T cells with both stimulations. Both T cell populations also produced IL-2 after stimulation with infected macrophages, whereas only CD4(+)T cells did when stimulated with TLA. CD4(+)immune T cells also produced large amounts of IL-4 and IL-10 after stimulation with infected macrophages, but CD8(+)T cells did not. These results indicate that CD4(+)immune T cells produce IFN-gamma, IL-2, IL-4, and IL-10 in response to infected macrophages, whereas CD8(+)immune T cells produce predominantly IFN-gamma and IL-2. Since IL-4 and IL-10 could suppress IFN-gamma-mediated protective mechanisms against the parasite, the production of these cytokines by CD4(+)immune T cells in response to infected cells could negatively affect their protective activity in vivo.
为了研究刚地弓形虫感染小鼠中CD4(+)免疫T细胞和CD8(+)免疫T细胞的细胞因子产生对感染细胞和寄生虫可溶性抗原的反应是否存在差异,我们比较了免疫T细胞群体在体外用速殖子感染的巨噬细胞和速殖子裂解物抗原(TLA)刺激后干扰素-γ(IFN-γ)、白细胞介素-2(IL-2)、IL-4和IL-10的产生情况。CD4(+)和CD8(+)免疫T细胞在受到感染的巨噬细胞或TLA刺激时都会产生大量的IFN-γ,但在两种刺激下,CD4(+)T细胞产生的这种细胞因子都比CD8(+)T细胞多。在用感染的巨噬细胞刺激后,两个T细胞群体也都会产生IL-2,而在用TLA刺激时,只有CD4(+)T细胞会产生IL-2。CD4(+)免疫T细胞在用感染的巨噬细胞刺激后也会产生大量的IL-4和IL-10,但CD8(+)T细胞不会。这些结果表明,CD4(+)免疫T细胞在受到感染的巨噬细胞刺激时会产生IFN-γ、IL-2、IL-4和IL-10,而CD8(+)免疫T细胞主要产生IFN-γ和IL-2。由于IL-4和IL-10可以抑制IFN-γ介导的针对该寄生虫的保护机制,CD4(+)免疫T细胞对感染细胞产生这些细胞因子可能会对其体内的保护活性产生负面影响。