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CXCR3+ Treg cells suppress Th1-immune responses through expression of the co-inhibitory receptors CD85k and Lag-3

ChEBI2018-06-30 更新2026-07-12 收录

调节性T细胞功能

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数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-MTAB-6156 数据链接链接失效反馈

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CXCR3+ Treg cells suppress Th1-immune responses through expression of the co-inhibitory receptors CD85k and Lag-3

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创建时间：

2018-06-30

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Triptolide possesses immunosuppressive activity and its efficacy is commonly believed to be related to the suppression of T cells. However, the underlying mechanism is still not well documented and mo

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Regulatory T cells in the Tumor Microenvironment Display a Unique Chromatin Accessibility Profile (ATAC-Seq). Regulatory T cells in the Tumor Microenvironment Display a Unique Chromatin Accessibility Profile (ATAC-Seq)

免疫表观遗传学

调节性T细胞功能

Regulatory T cells (Tregs) are a suppressive CD4+ T cell population that limit the anti-tumor immune response. In this study, we analyzed the chromatin accessibility of Tregs in the murine tumor micro

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Dysregulated expression of genes in regulatory T cells from metastatic castration-resistant prostate cancer patients

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调节性T细胞功能

Dysregulated expression of genes in regulatory T cells from metastatic castration-resistant prostate cancer patients

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Expression Data from regulatory T-cells in a model of acute pancreatitis. Expression Data from regulatory T-cells in a model of acute pancreatitis

调节性T细胞功能

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Foxp3 positive regulatory T-cells were isolated by FACS from spleen of mice with acute pancreatitis induced by partial pancreatic duct ligation, mice without pancreatitis refer as controls we used mic

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Dissecting the immune suppressive human prostate tumor microenvironment via integrated single-cell and spatial transcriptomic analyses

肿瘤微环境

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Novel single cell technologies have paved the way for the characterization and improved biological understanding of prostate cancer, here we performed scRNA-seq on 20 human prostate tumors and their m

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CXCR3+ Treg cells suppress Th1-immune responses through expression of the co-inhibitory receptors CD85k and Lag-3

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