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Functional Analysis of Dendritic Cells Generated from T-iPSCs from CD4+ T Cell Clones of Sj?gren's Syndrome

机译:Sj?gren综合征CD4 + T细胞克隆T-iPSC产生的树突状细胞的功能分析

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Summary Although it is important to clarify the pathogenic functions of T?cells in human samples, their examination is often limited due to difficulty in obtaining sufficient numbers of dendritic cells (DCs), used as antigen-presenting cells, especially in autoimmune diseases. We describe the generation of {DCs} from induced pluripotent stem cells derived from T?cells (T-iPSCs). We reprogrammed CD4+ T?cell clones from a patient with Sj?gren's syndrome (SS) into iPSCs, which were differentiated into {DCs} (T-iPS-DCs). T-iPS-DCs had dendritic cell-like morphology, and expressed CD11c, HLA-DR, CD80, CD86, and also BDCA-3. Compared with monocyte-derived DCs, the capacity for antigen processing was similar, and T-iPS-DCs induced the proliferative response of autoreactive CD4+ T?cells. Moreover, we could evaluate T?cell functions of the patient with SS. In conclusion, we obtained adequate numbers of {DCs} from T-iPSCs, which could be used to characterize pathogenic T?cells in autoimmune diseases such as SS.
机译:总结尽管弄清人类样品中T细胞的致病功能很重要,但由于难以获得足够数量的树突状细胞(DC)用作抗原呈递细胞,特别是在自身免疫性疾病中,它们的检查常常受到限制。我们描述了从T细胞(T-iPSCs)衍生的诱导多能干细胞产生{DCs}。我们将患有干燥综合征(SS)患者的CD4 + T细胞克隆重编程为iPSC,然后将其分化为{DCs}(T-iPS-DCs)。 T-iPS-DC具有树突状细胞形态,并表达CD11c,HLA-DR,CD80,CD86和BDCA-3。与单核细胞衍生的DC相比,抗原加工的能力是相似的,并且T-iPS-DC诱导了自身反应性CD4 +Tβ细胞的增殖反应。此外,我们可以评估SS患者的T细胞功能。总之,我们从T-iPSC中获得了足够数量的{DCs},可用于表征自身免疫性疾病(如SS)中的致病性T细胞。

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