Heterogeneity of changes in lymphoproliferative ability with increasing age
D M Murasko1, B J Nelson, D Matour
1Department of Microbiology, Medical College of Pennsylvania, Philadelphia 19129.
Insights
Aging reduces lymphoproliferation, but individual responses vary greatly. Interleukin-2 (IL-2) levels and responses to supplemental IL-2 also show significant heterogeneity in elderly individuals.
Area of Science:
- Immunology
- Gerontology
- Cellular Biology
Background:
- Immune function, including lymphoproliferation, generally declines with age.
- Significant individual variability exists in immune responses among elderly populations.
Purpose of the Study:
- To investigate the heterogeneity in mitogen-induced lymphoproliferation and interleukin-2 (IL-2) production in aging individuals.
- To determine the impact of exogenous IL-2 on lymphoproliferation in elderly subjects.
- To explore the influence of genetic factors on age-related changes in immune responses.
Main Methods:
- Measurement of mitogen-induced lymphoproliferation in human subjects.
- Quantification of detectable interleukin-2 (IL-2) levels post-stimulation.
- Assessment of proliferation response following exogenous IL-2 administration.
- Analysis of immune responses in inbred rat strains under controlled conditions.
Main Results:
- Individual variations in lymphoproliferation and IL-2 levels were observed in elderly subjects.
- Exogenous IL-2 supplementation enhanced proliferation in approximately one-third of elderly participants.
- Genetic factors significantly impact proliferation levels and age-related decline, with variation present even within inbred rat strains.
Conclusions:
- Age-related decline in lymphoproliferation is characterized by substantial individual heterogeneity.
- Interleukin-2 (IL-2) availability and response are key factors contributing to this variability.
- Genetic background plays a crucial role in modulating immune responses during aging.
Abstract:
Although mean mitogen-induced lymphoproliferation decreases with increased age, the response of individual subjects demonstrates great heterogeneity. Results of this study clearly illustrate that individual variation is apparent not only in the level of proliferation, but also in the amount of interleukin-2 (IL-2) detectable after mitogen stimulation. Further, addition of exogenous IL-2 significantly increases proliferation in only about one third of elderly subjects. Data from inbred strains of rats housed under identical environmental conditions indicate that although genetic factors greatly influence both the level of proliferation and the rate of decline with age, variation occurs even within one inbred strain of rat.
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