IL-10和TGF-β,但不是IL-17A或IFN-γ,增强IL-15诱导的人类T细胞的增殖:与IL-15诱导的无β2mHLA类I分子表达的减少有关
Leila H Duarte1, Hugo A Peixoto1, Elsa M Cardoso1,2
1CICS-UBI, Health Sciences Research Centre, University of Beira Interior, 6200-506 Covilhã, Portugal.
International journal of molecular sciences
|September 14, 2024
概括
介素-10 (IL-10) 和转化生长因子-β (TGF-β) 增强IL-15驱动的人类T细胞的增殖. 这种增强与减少HLA类I分子的表达有关,影响免疫反应.
科学领域:
- 免疫学 免疫学 免疫学
- 细胞生物学 细胞生物学
背景情况:
- 介质素-15 (IL-15) 对于T和NK细胞恒温至关重要.
- 其他细胞因子对IL-15对T细胞的影响的影响在很大程度上是未知的.
研究的目的:
- 研究IL-10,TGF-β,IL-17A和IFN-γ如何影响IL-15诱导的T细胞增殖.
- 检查这些细胞因子在T细胞激活过程中对HLA类I (HLA-I) 分子表达的影响.
主要方法:
- 人类周围血液淋巴细胞 (PBLs) 被标记为CFSE.
- 细胞被单独使用IL-15或与IL-10,TGF-β,IL-17A或IFN-γ结合刺激了12天.
- 通过流式细胞计量分析了T细胞增殖和细胞表面HLA-I表达.
主要成果:
- 刺激IL-15增加了T细胞的增殖和HLA-I的表达,特别是在高度分裂的细胞上.
- IL-10和TGF-β显著增强了IL-15诱导的T细胞增殖.
- IL-10和TGF-β治疗与HC-10反应性HLA-I分子的表达减少有关.
结论:
- 在实验室中,IL-10和TGF-β增强了受IL-15刺激的人类T细胞的增殖能力.
- 这种IL-10和TGF-β的增强与IL-15诱导的HLA I类分子表达的减少有关.
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