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Effects of TNF-alpha blocking in sorted Th17 cells from co-cultures of human CD4-positive and CD14-positive cells

ChEBI2013-11-01 更新2026-07-21 收录

Th17细胞免疫

TNF-α阻断治疗评估

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https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-51540 数据链接链接失效反馈

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Effects of TNF-alpha blocking in sorted Th17 cells from co-cultures of human CD4-positive and CD14-positive cells

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创建时间：

2013-11-01

Th17细胞免疫

植物提取物药效

Naive CD4+ T cells differentiate into effector (Th1, Th2, Th17) cells and immunosuppressive (Treg) cells upon antigenic stimulation in the presence of a specific cytokine milieu. The T cell in vitro c

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Human Th17 cells engage gasdermin E pores to release IL-1alpha upon NLRP3 inflammasome activation

Th17细胞免疫

病原-宿主互作

Adaptive immune responses are tailored to the invading microbial antigen and tissue microenvironment, resulting in diverse context-specific inflammatory signatures. There is emerging evidence that inn

NIAID Data Ecosystem70

Th17 Cells Are More Protective Than Th1 Cells Against the Intracellular Parasite Trypanosoma cruzi

Th17细胞免疫

恰加斯病免疫治疗

Th17 cells are a subset of CD4+ T cells known to play a central role in the pathogenesis of many autoimmune diseases, as well as in the defense against some extracellular bacteria and fungi. However,

NIAID Data Ecosystem60

Effect of Itolizumab on Th17 polarized cells. Homo sapiens

Th17细胞免疫

药物基因表达

In this study the Itolizumab treated group is compared to control treated group across days in polarizing conditions Overall design: Agilent Custom Human Gene Expression 8X15k (AMADID: 16332) designed

NIAID Data Ecosystem70

CD161 Expression Defines a Th1/Th17 Polyfunctional Subset of Resident Memory T Lymphocytes in Bronchoalveolar Cells

组织驻留记忆T细胞

Th17细胞免疫

Alveolar resident memory T cells (TRM) comprise a currently uncharacterized mixture of cell subpopulations. The CD3+CD161+ T cell subpopulation resides in the liver, intestine and skin, but it has the

NIAID Data Ecosystem60

Effects of TNF-alpha blocking in sorted Th17 cells from co-cultures of human CD4-positive and CD14-positive cells

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