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Trained Immunity: Long-Term Adaptation in Innate Immune Responses
Helin Tercan1, Niels P Riksen1, Leo A B Joosten1,2
1Department of Internal Medicine and Research Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, the Netherlands (H.T., N.P.R., L.A.B.J., M.G.N., S.B.).
Innate immune cells can develop trained immunity, a persistent hyperresponsive state after stimulation. This trained immunity offers protection against infections but can worsen chronic inflammatory diseases.
Area of Science:
- Immunology
- Cellular Biology
- Infectious Disease
Background:
- Adaptive immunity features antigen specificity and long-term immunologic memory.
- Innate immune cells can also develop memory, a process known as trained immunity.
- Trained immunity involves a persistent hyperresponsive phenotype in innate immune cells following brief stimulation.
Purpose of the Study:
- To explore the concept of trained immunity in innate immune cells.
- To understand the mechanisms and implications of trained immunity.
- To investigate the potential of trained immunity in disease treatment and vaccination.
Main Methods:
- Review of recent scientific literature on trained immunity.
- Analysis of stimuli that induce trained immunity in monocytes and macrophages.
- Examination of epigenetic and metabolic mechanisms underlying trained immunity.
Main Results:
- Pathogenic stimuli and endogenous molecules can induce trained immunity.
- Trained immunity provides cross-protection against infections but can exacerbate chronic inflammation (e.g., atherosclerosis).
- Trained immunity is maintained by epigenetic and metabolic reprogramming, persisting for months due to myeloid progenitor cell changes.
Conclusions:
- Trained immunity involves epigenetic and metabolic reprogramming, affecting myeloid progenitor cells.
- This phenomenon can be beneficial for infectious disease protection but detrimental in chronic inflammatory conditions.
- Trained immunity offers a novel framework for developing new vaccines and therapeutic targets for inflammatory diseases.
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