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Antigen-Specific Regulation of IgE Antibodies by Non-Antigen–Specific γδ T Cells

机译:非抗原特异性γδT细胞对IgE抗体的抗原特异性调节

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We re-examined the observation that γδ T cells, when transferred from mice tolerized to an inhaled conventional Ag, suppress the allergic IgE response to this Ag specifically. Using OVA and hen egg lysozyme in crisscross fashion, we confirmed the Ag-specific IgE-regulatory effect of the γδ T cells. Although only Vγ4+ γδ T cells are regulators, the Ag specificity does not stem from specificity of their γδ TCRs. Instead, the Vγ4+ γδ T cells failed to respond to either Ag, but rapidly acquired Ag-specific regulatory function in vivo following i.v. injection of non-T cells derived from the spleen of Ag-tolerized mice. This correlated with their in vivo Ag acquisition from i.v. injected Ag-loaded splenic non-T cells, and in vivo transfer of membrane label provided evidence for direct contact between the injected splenic non-T cells and the Vγ4+ γδ T cells. Together, our data suggest that Ag itself, when acquired by γδ T cells, directs the specificity of their IgE suppression.
机译:我们重新检查了观察结果,即当γδT细胞从可耐受吸入常规Ag的小鼠转移时,会特异性抑制对该Ag的过敏性IgE反应。交叉使用OVA和鸡蛋溶菌酶,我们证实了γδT细胞的银特异性IgE调节作用。尽管只有Vγ4+γδT细胞是调节因子,但Ag特异性并非源于其γδTCR的特异性。取而代之的是,Vγ4+γδT细胞对两种Ag均无反应,但在静脉内注射后迅速在体内获得了Ag特异性调节功能。注射来自耐受银的小鼠脾脏的非T细胞。这与他们从i.v.注射的载有Ag的脾脏非T细胞,以及体内膜标记的转移为注射的脾脏非T细胞与Vγ4+γδT细胞之间的直接接触提供了证据。总之,我们的数据表明,当被γδT细胞获取时,Ag本身指导其IgE抑制的特异性。

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