About this Research Topic
T cell populations including CD4+ helper T cells, CD8+ cytotoxic T cells and Foxp3+ regulatory T cells play a critical role in controlling or promoting inflammatory disease’s progression. In recent years, therapeutic regimens targeting specific T cell populations have exhibited potential value in treating a series of diseases. In the specific context of inflammatory diseases, cytokines, co-stimulatory molecules and metabolic products have an intensive impact on tissue-infiltrated T cell populations, which are prone to differentiate into multiple T cell subsets with distinct characteristics and functions, leading to disease’s control or progression. Thereby, to explore the factors and signal mechanisms that influence the function and regulation of T cell subsets in the circumstances of inflammatory diseases is of great significance for guiding immunotherapy through manipulating specific T cell subsets.
The goal of this Research Topic is to provide a forum to advance research on uncovering the factors and signal pathways that modulate T cell differentiation, proliferation, migration, metabolism and exhaustion in various disease settings. In addition, the special section also welcomes the submission that discover new strategies targeting specific T cell subsets, and the translation in clinic.
We warmly welcome the submissions of Original Research and Review on the sub-topics below:
• Novel T cell subsets in the context of inflammatory diseases
• Factors and signal mechanisms that mediate differentiation of T cell subsets in the context of inflammatory diseases
• T cell exhaustion and migration in the tissue microenvironment of inflammatorydiseases
• Tissue-specific Treg cells in inflammatory diseases
• Mechanism of Treg differentiation and expansion in inflammatory diseases
• The metabolism of T cells in the tissue microenvironment of inflammatory diseases
• The function of T cell subsets in response to cytokines and costimulatory molecules
The Research Topic Editors declare that they have no conflicts of interest arising in relation to their roles in the development and editorial of this collection.
The goal of this Research Topic is to provide a forum to advance research on uncovering the factors and signal pathways that modulate T cell differentiation, proliferation, migration, metabolism and exhaustion in various disease settings. In addition, the special section also welcomes the submission that discover new strategies targeting specific T cell subsets, and the translation in clinic.
We warmly welcome the submissions of Original Research and Review on the sub-topics below:
• Novel T cell subsets in the context of inflammatory diseases
• Factors and signal mechanisms that mediate differentiation of T cell subsets in the context of inflammatory diseases
• T cell exhaustion and migration in the tissue microenvironment of inflammatorydiseases
• Tissue-specific Treg cells in inflammatory diseases
• Mechanism of Treg differentiation and expansion in inflammatory diseases
• The metabolism of T cells in the tissue microenvironment of inflammatory diseases
• The function of T cell subsets in response to cytokines and costimulatory molecules
The Research Topic Editors declare that they have no conflicts of interest arising in relation to their roles in the development and editorial of this collection.
Keywords: Novel T cell subsets, Differentiation of T cell subsets, T cell exhaustion, Tissue-specific Treg cells, Metabolism of T cells, T cell immunotherapy
Important Note: All contributions to this Research Topic must be within the scope of the section and journal to which they are submitted, as defined in their mission statements. Frontiers reserves the right to guide an out-of-scope manuscript to a more suitable section or journal at any stage of peer review.
