Adaptive Immune Regulation of Non-Alcoholic Steatohepatitis (NASH)

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About this Research Topic

Submission deadlines

  1. Manuscript Submission Deadline 30 April 2025 | Manuscript Extension Submission Deadline 31 May 2025

  2. This Research Topic is still accepting articles.

Background

Non-Alcoholic Steatohepatitis (NASH) is a severe manifestation of non-alcoholic fatty liver disease (NAFLD), characterized by hepatic inflammation and fibrosis. A critical yet underexplored aspect of NASH pathogenesis is the role of adaptive immunity. Adaptive immune cells, including various T and B cell subsets, play significant roles in the inflammatory processes that contribute to both liver damage and repair. These cells interact with the innate immune system, forming a complex immune network that influences the progression of NASH. Recent studies have highlighted the importance of understanding these interactions to unravel the underlying mechanisms of NASH. However, despite advances in the field, comprehensive insights into the adaptive immune regulation of NASH remain fragmented. There is a pressing need for more detailed investigations to bridge these knowledge gaps and to explore the potential of adaptive immunity as a target for diagnostic and therapeutic strategies .

This research topic aims to dissect and elucidate the multifaceted roles of adaptive immune regulation in NASH. The primary objectives include understanding how different T cell subsets, such as exhausted CD8, effector CD8, memory CD8, Th1, Th2, Th17, and Tregs, balance pro-inflammatory and anti-inflammatory responses. Additionally, the research will explore the involvement of B cells in antibody-mediated reactions and the cross-talk between adaptive and innate immunity through mechanisms like Toll-like receptor signaling. By integrating these insights, the research aims to foster translational applications that could lead to the development of diagnostic biomarkers and personalized therapeutic strategies for NASH.

To gather further insights into the adaptive immune regulation of NASH, we welcome articles addressing, but not limited to, the following themes:
- Characterization of T cell and B cell subsets and their roles in NASH.
- Molecular mechanisms underlying adaptive immune responses in NASH, including cytokines, chemokines, and signaling pathways.
- Interplay between adaptive and innate immunity, including the roles of myeloid-derived suppressor cells and innate lymphoid cells.
- Clinical applications of adaptive immune insights, such as biomarker discovery, therapeutic targeting, and potential links with other immune-mediated inflammatory diseases (IMIDs).
- Ethical, clinical, and translational considerations in the study and treatment of NASH through adaptive immunity.

Manuscripts describing traditional or alternative medicine are out of scope for this Research Topic .

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Keywords: Non-Alcoholic Steatohepatitis, Adaptive Immunity, T cells, exhausted CD8, effector CD8, memory CD8, Th1, Th2, Th17, Tregs, B cells, Immunotherapy, Inflammation, Biomarkers, Toll-like Receptors, Myeloid-derived Suppressor Cells, Innate Lymphoid Cells

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