Abstract
Immune surveillance and adaptive immune responses, involving continuously circulating and tissue-resident T-lymphocytes, provide host defense against infectious agents and possible malignant transformation while avoiding autoimmune tissue damage. Activation, migration, and deployment of T-cells to affected tissue sites are crucial for mounting an adaptive immune response. An effective adaptive immune defense depends on the ability of T-cells to dynamically reprogram their metabolic requirements in response to environmental cues. Inability of the T-cells to adapt to specific metabolic demands may skew cells to become either hyporesponsive (creating immunocompromised conditions) or hyperactive (causing autoimmune tissue destruction). Here, we review maladaptive T-cell metabolic fitness that can cause autoimmune diseases and discuss how T-cell metabolic programs can potentially be modulated to achieve therapeutic benefits.
Original language | English |
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Article number | 2541 |
Journal | Cells |
Volume | 12 |
Issue number | 21 |
DOIs | |
Publication status | Published - Nov 2023 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2023 by the authors.
ASJC Scopus Subject Areas
- General Biochemistry,Genetics and Molecular Biology
Keywords
- autoimmunity
- glycolysis
- LFA-1
- metabolites
- psoriasis
- rheumatoid arthritis
- T-cell function
- T-cell motility
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Recent Findings in Autoimmunity Described by a Researcher from Nanyang Technological University (Maladaptive T-Cell Metabolic Fitness in Autoimmune Diseases)
11/15/23
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