Abstract
Adaptive immunity plays a crucial role of protection of our body from pathogens while its deregulation leads to allergy and autoimmunity. T cells represent a major branch of lymphocytes, which are responsible for adaptive immunity, which represent a major pathway of immune function, which depend on their T-cell regulation. Cytokines also contribute to regulation. Over the past two decades, epigenetic mechanisms have been increasingly recognized to play a fundamental role in the proper execution of genetic programs that regulate immune function. The role of epigenetics in T-cell development and function (collectively called T-cell biology here) has been intensively studied, and epigenetic machinery is emerging as a potential therapeutic target to cure allergy and autoimmunity or to enhance immune response and immunological memory. In this article, the current findings and progresses of epigenetic study in T-cell biology are reviewed, focusing on genetic studies of so called epigenetic “writers” and “erasers” that catalyze addition and removal of covalent DNA and histone modifications.
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