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通过用Toll样受体9配体激活CD8 +小鼠树突状细胞,将受限的CD4 T细胞反应转变为有效的反应。

Switching from a restricted to an effective CD4 T cell response by activating CD8+ murine dendritic cells with a Toll-like receptor 9 ligand.

作者信息

Rizzitelli Alexandra, Vremec David, Villadangos Jose A, Mavaddat Nasim, Wright Mark D, Shortman Ken

机构信息

The Walter and Eliza Hall Institute of Medical Research, Parkville, Victoria, Australia.

出版信息

Eur J Immunol. 2005 Nov;35(11):3209-20. doi: 10.1002/eji.200526231.

Abstract

Freshly isolated quiescent splenic dendritic cell (DC) subtypes differ in their capacity to activate naive CD4 T cells in culture. The CD8+ DC showed a reduced capacity to stimulate T cell proliferation compared to either of the CD8- DC subsets, regardless of antigen and DC dose. In contrast to CD8- DC, the quiescent CD8+ DC did not induce IFN-gamma production from CD4 T cells. The difference between the DC subtypes appeared to be at the level of initial surface molecule interactions, but could not be attributed to differences in expression of MHC class II or B7 family molecules, or to the expression of Fas ligand on DC. However, when activated by inclusion of the Toll-like receptor 9 ligand CpG in culture, CD8+ DC became potent stimulators of both CD4 T cell proliferation and IFN-gamma production. In contrast, similar activation of CD8- DC produced a more modest increase in capacity to stimulate CD4 T cell proliferation and no increase in capacity to stimulate IFN-gamma production. The difference between a quiescent and an activated state is therefore more extreme for CD8+ than for CD8- DC. The especially tight regulation of the activity of CD8+ DC may be essential for the maintenance of self tolerance.

摘要

新鲜分离的静止脾树突状细胞(DC)亚型在体外培养中激活初始CD4 T细胞的能力有所不同。无论抗原和DC剂量如何,与两种CD8 - DC亚群相比,CD8 + DC刺激T细胞增殖的能力均降低。与CD8 - DC相反,静止的CD8 + DC不会诱导CD4 T细胞产生IFN - γ。DC亚型之间的差异似乎出现在初始表面分子相互作用水平,但不能归因于MHC II类分子或B7家族分子表达的差异,也不能归因于DC上Fas配体的表达。然而,当在培养中加入Toll样受体9配体CpG激活时,CD8 + DC成为CD4 T细胞增殖和IFN - γ产生的有效刺激物。相反,CD8 - DC的类似激活在刺激CD4 T细胞增殖的能力上产生了更适度的增加,而在刺激IFN - γ产生的能力上没有增加。因此,静止状态和激活状态之间的差异对于CD8 + DC比对于CD8 - DC更为极端。对CD8 + DC活性的特别严格调控可能对于维持自身耐受性至关重要。

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