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Granulocyte and natural killer activity in the elderly
G Di Lorenzo1, C R Balistreri, G Candore
1Istituto di Medicina interna e Geriatria dell'Università di Palermo, Italy.
Mechanisms of Ageing and Development
|June 12, 1999
Summary
Ageing impairs innate immunity, decreasing neutrophil function and natural killer (NK) cell activity. This age-related decline in non-specific immunity contributes to immunosenescence, increasing susceptibility to infections in the elderly.
Area of Science:
- Immunology
- Gerontology
- Cellular Biology
Background:
- Ageing leads to immunosenescence, a decline in immune system function.
- This decline is linked to increased susceptibility to infections, autoimmune diseases, and cancer.
- While T-cell changes are known, the impact on non-specific immunity requires further investigation.
Purpose of the Study:
- To investigate age-related changes in neutrophil (PMN) function, including superoxide production, chemotaxis, and apoptosis.
- To assess age-related differences in basal natural killer (NK) cell activity and CD16+ cell numbers.
- To determine the role of these innate immune changes in the overall process of immunosenescence.
Main Methods:
- Assessed superoxide production and chemotaxis in neutrophils from young and elderly subjects.
- Measured APO1/Fas (CD95) expression on neutrophils to evaluate apoptosis.
- Quantified basal NK activity and the number of CD16+ cells in young and elderly individuals.
Main Results:
- Significant age-related decreases in neutrophil superoxide production and chemotaxis were observed.
- No significant correlation was found between age and CD95 expression on neutrophils.
- A significant age-related decrease in NK cell activity was noted, despite an increased number of CD16+ cells in the elderly.
Conclusions:
- Immunosenescence involves a decline in non-specific immunity, including impaired neutrophil function and reduced NK cell activity.
- Decreased neutrophil function is not primarily driven by CD95-mediated apoptosis.
- The findings highlight deficits in innate immunity as a significant factor in the pathogenesis of immunosenescence.