Turku Centre for Biotechnology, University of Turku and Åbo Akademi University, Turku, Finland.
Scand J Immunol. 2013 Aug;78(2):172-80. doi: 10.1111/sji.12071.
Current knowledge of helper T cell differentiation largely relies on data generated from mouse studies. To develop therapeutical strategies combating human diseases, understanding the molecular mechanisms how human naïve T cells differentiate to functionally distinct T helper (Th) subsets as well as studies on human differentiated Th cell subsets is particularly valuable. Systems biology approaches provide a holistic view of the processes of T helper differentiation, enable discovery of new factors and pathways involved and generation of new hypotheses to be tested to improve our understanding of human Th cell differentiation and immune-mediated diseases. Here, we summarize studies where high-throughput systems biology approaches have been exploited to human primary T cells. These studies reveal new factors and signalling pathways influencing T cell differentiation towards distinct subsets, important for immune regulation. Such information provides new insights into T cell biology and into targeting immune system for therapeutic interventions.
目前关于辅助性 T 细胞分化的知识主要依赖于从鼠类研究中获得的数据。为了开发针对人类疾病的治疗策略,了解人类初始 T 细胞分化为功能不同的辅助性 T 细胞(Th)亚群的分子机制,以及对人类分化的 Th 细胞亚群的研究是特别有价值的。系统生物学方法为辅助性 T 细胞分化过程提供了一个整体的视角,能够发现新的参与因子和途径,并生成新的假说进行验证,以提高我们对人类 Th 细胞分化和免疫介导疾病的理解。在这里,我们总结了利用高通量系统生物学方法研究人类原代 T 细胞的研究。这些研究揭示了影响 T 细胞向不同亚群分化的新的因子和信号通路,这对于免疫调节非常重要。这些信息为 T 细胞生物学和针对免疫系统的治疗干预提供了新的见解。