6533b7cefe1ef96bd1257ab7
RESEARCH PRODUCT
The effect of age on mitogen responsive T cell precursors in human beings is completely restored by interleukin-2.
Gabriele Di LorenzoGiuseppe Barbagallo SangiorgiAlfredo SalernoCalogero CarusoGiuseppina CandoreMaria Assunta ModicaGrazia CrescimannoAntonio Tobia ColucciA. Ingrassiasubject
Interleukin 2AdultMalemedicine.medical_specialtyAgingmedicine.medical_treatmentT cellT-LymphocytesIn Vitro TechniquesLymphocyte ActivationInternal medicinemedicineConcanavalin AHumansAgedAged 80 and overbiologyCell growthT lymphocyteMiddle AgedHematopoietic Stem CellsIn vitroEndocrinologyCytokinemedicine.anatomical_structureConcanavalin AAgeingImmunologybiology.proteinInterleukin-2FemaleDevelopmental Biologymedicine.drugdescription
Abstract It is well known that the function of T lymphocytes is significantly impaired by advancing age. In the present study, attempts have been made to further characterize the T cell impairment of elderly subjects. Thus, we have performed limiting dilution microculture analysis to evaluate the precursor frequency of T lymphocytes responding to a mitogenic stimulus in old and young subjects. Furthermore we have evaluated the activity of recombinant interleukin-2 (rIL-2) on these cells. The results demonstrate that in older subjects the frequency of these precursors is significantly decreased. The in vitro treatment with rIL-2 increased the frequency of mitogen responsive T lymphocyte precursors in both groups so that the difference between the two groups was not significant. Thus present results extend the finding demonstrating that older subjects display an impairment of T cell functions and that IL-2 treatment may correct these alterations. In particular, they confirm the hypothesis that age-associated functional changes are more likely due to diminished numbers of reactive cells, than to a decline in the activity of all cells.
year | journal | country | edition | language |
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1992-05-01 | Mechanisms of ageing and development |