Defect of autologous mixed lymphocyte reaction and interleukin-2 in aged individuals

Mech Ageing Dev. 1985 Nov;32(2-3):205-12. doi: 10.1016/0047-6374(85)90080-6.

Abstract

The proliferative responsiveness of T cells of aged individuals is known to be depressed in both autologous mixed lymphocyte reaction (AMLR) and in PHA-stimulated cultures. In the present study we confirm previous results and also report decreased IL-2 and normal IFN-gamma production (PHA-induced) in aged subjects as compared to young normals. In addition, similar percentages of T lymphocytes expressing surface IL-2 receptors both in the peripheral blood and after different stimulations, i.e. AMLR and PHA, were detected in young and aged individuals. The addition of exogenous IL-2 induces a sharp increase of spontaneous and AMLR proliferation in young individuals, whereas the increase is only slight in aged subjects. The experiments reported herein suggest that in general the T cell proliferation in AMLR is not completely dependent on the presence of IL-2 in the cultures and that aged subjects are probably defective in the production of other factor(s) presumably involved in AMLR proliferation, since the addition of exogenous IL-2 does not produce T-cell proliferation comparable to normal young subjects. The possible meanings of these experimental evidences in AMLR and in the defective immune responses of aged subjects are discussed.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aged
  • Aging
  • Cells, Cultured
  • Female
  • Humans
  • Interleukin-2 / immunology*
  • Kinetics
  • Lymphocyte Activation*
  • Lymphocyte Culture Test, Mixed
  • Male
  • Receptors, Immunologic / analysis
  • Receptors, Interleukin-2
  • T-Lymphocytes / cytology
  • T-Lymphocytes / immunology*

Substances

  • Interleukin-2
  • Receptors, Immunologic
  • Receptors, Interleukin-2