首页> 美国卫生研究院文献>Ophthalmology and Eye Diseases >The Induction of Circulating ACAID-Inducing Monocytes Requires CCR2/CCL2-Dependent Migration of Circulating F4/80+ Cells into the Anterior Chamber
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The Induction of Circulating ACAID-Inducing Monocytes Requires CCR2/CCL2-Dependent Migration of Circulating F4/80+ Cells into the Anterior Chamber

机译:循环诱导ACAID的单核细胞的诱导需要循环F4 / 80 +细胞进入前房的CCR2 / CCL2依赖性迁移。

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摘要

To determine the origin of peripheral blood mononulclear cells (PBMC) that activate regulatory T cells in anterior chamber-associated immune deviation (ACAID), fluorescein-labeled PBMC were intravenously injected into mice before the mice received an intracameral injection of antigen. Six-24 hr after intracameral injection, fluorescein-labeled PBMC increased in the iris. Twenty-four-48 hr labeled cells decreased in the iris and increased in the thymus and spleen. The entry of the labeled PBMC into the anterior chamber and subsequent production of PBMC that transfer ACAID required the expression of CCR2 by the PBMC and the production of the chemokine CCL2 by the recipient of the PBMC. The results suggest that the intracameral injection of antigen induces i) the infiltration of F4/80+ PBMC into the AC, ii) where these PBMC are converted to a regulatory phenotype, and iii) recirculate to activate T cells that suppress cell-mediated immunity.
机译:为了确定激活前房相关免疫偏差(ACAID)中调节性T细胞的外周血单核细胞(PBMC)的起源,在小鼠接受前房内注射抗原之前,将荧光素标记的PBMC静脉内注射入小鼠。前房内注射后6-24小时,虹膜中荧光素标记的PBMC增加。 24-48小时标记的细胞在虹膜中减少,在胸腺和脾脏中增加。标记的PBMC进入前房并随后产生转移ACAID的PBMC需要PBMC表达CCR2,而PBMC的接受者则需要产生趋化因子CCL2。结果表明,抗原的前房内注射诱导i)F4 / 80 + PBMC浸入AC,ii)这些PBMC转化为调节表型,并且iii)再循环以激活T抑制细胞介导的免疫力的细胞。

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