Cellular senescence: Immunosurveillance and future immunotherapy
Open accessAbstract
In response to persistent DNA damage, induction into cell senescence promotes an immunogenic program which facilitates immune clearance of these damaged cells. Under physiological conditions, senescent cells can activate both innate and adaptive immune responses, functioning to maintain tissue homeostasis. In addition, emerging findings suggest that programmed induction of cell senescence may be important for regulating reproductive processes, partly facilitated by immune clearance. However, likely owing to ageing of the immune system, a failure to eliminate senescent cells can contribute to their persistence in tissues, leading to the development and progression of age-related diseases. Such immune failure may in part be due to activation of the senescence program in immune cells, leading to their dysfunction. Furthermore, senescent cells under certain biological contexts have been shown to instead promote immune suppression, a response that may reflect differences between an acute verses chronic senescent phenotype. In this review, we provide an overview of the research to date concerning senescence immunosurviellance, including a focused discussion on the mechanisms by which macrophages may recognise senescent cells. Senescence immunotherapy strategies as an alternative to senolytics for the removal of senescent cells will also be discussed.
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Senescent cells are usually cleared by macrophages and NK cells.
“senescent cells are usually cleared by macrophages and NK cells, 255”
From Meta-hallmarks of aging and cancer (2023) · cites this paper as [255]
Aging of the immune system may hamper the efficient removal of senescent cells and contribute to their progressive accumulation.
“Aging of the immune system may hamper the efficient removal of senescent cells and contribute to their progressive accumulation (38).”
From Exercise Counters the Age-Related Accumulation of Senescent Cells (2022) · cites this paper as [38]
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References 115 · Cited by 221
- Authors
- Burton, D. G. A., & Stolzing, A.
- Affiliations
- Loughborough University (GB)
- Corresponding author
- Burton, Dominick G.A.
- Venue
- Ageing Research Reviews
- Publisher
- Elsevier BV
- Published
- 2018-05
- Volume
- 43
- Pages
- 17-25
- ISSN
- 1568-1637 (ISSN-L)
- OpenAlex
- W2790749994
- Cited by
- 221
- References
- 115
- Citations by year
- 2026: 13 · 2025: 26 · 2024: 26 · 2023: 29 · 2022: 25 · 2021: 31 · 2020: 37 · 2019: 23 · 2018: 11
- FWCI
- 3.35
- Type
- journal article
- Language
- en
- Open access
- green
- dspace.lboro.ac.uk
- Licence
- cc-by-nc-nd
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- Locations
- Ageing Research Reviews (publishedVersion)
- PubMed (publishedVersion)
- Loughborough University Institutional Repository (Loughborough University) (submittedVersion, cc-by-nc-nd)
- Loughborough University Research Repository (Loughborough University) (submittedVersion, cc-by-nc-nd)
- Topics
- Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Immunology and Microbiology › Immunology › Phagocytosis and Immune Regulation
- Keywords
- cellular senescence, DNA damage response, innate and adaptive immunity, tissue homeostasis, reproductive processes, immunosenescence, age-related diseases, immunosuppression, senolytics
- MeSH terms
- Animals, DNA Damage, Forecasting, Humans, Immunity, Cellular, Immunotherapy, Macrophages, Monitoring, Immunologic, Cellular Senescence
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