Immunosenescence, Inflammaging, and Frailty: Role of Myeloid Cells in Age-Related Diseases.
Augusto BleveFrancesca MottaBarbara DuranteChiara PandolfoCarlo Francesco SelmiAntonio SicaPublished in: Clinical reviews in allergy & immunology (2022)
The immune system is the central regulator of tissue homeostasis, ensuring tissue regeneration and protection against both pathogens and the neoformation of cancer cells. Its proper functioning requires homeostatic properties, which are maintained by an adequate balance of myeloid and lymphoid responses. Aging progressively undermines this ability and compromises the correct activation of immune responses, as well as the resolution of the inflammatory response. A subclinical syndrome of "homeostatic frailty" appears as a distinctive trait of the elderly, which predisposes to immune debilitation and chronic low-grade inflammation (inflammaging), causing the uncontrolled development of chronic and degenerative diseases. The innate immune compartment, in particular, undergoes to a sequela of age-dependent functional alterations, encompassing steps of myeloid progenitor differentiation and altered responses to endogenous and exogenous threats. Here, we will review the age-dependent evolution of myeloid populations, as well as their impact on frailty and diseases of the elderly.
Keyphrases
- community dwelling
- low grade
- dendritic cells
- bone marrow
- acute myeloid leukemia
- inflammatory response
- immune response
- innate immune
- high grade
- induced apoptosis
- middle aged
- oxidative stress
- stem cells
- transcription factor
- signaling pathway
- cell cycle arrest
- genome wide
- toll like receptor
- lipopolysaccharide induced
- gene expression
- single molecule
- endoplasmic reticulum stress
- drug induced
- lps induced
- antimicrobial resistance
- multidrug resistant
- cell proliferation