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Related Experiment Videos

Demonstration of a thymus derived, splenic suppressor cell responsible for the age-dependent decrease in contact

G Roupe, L Lindholm

    The Journal of Investigative Dermatology
    |April 1, 1979
    PubMed
    Summary

    Aging mice show reduced contact hypersensitivity due to splenic suppressor T cells. These cells primarily inhibit the elicitation phase of allergic contact sensitivity reactions.

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    Area of Science:

    • Immunology
    • Allergy Research
    • T cell immunology

    Background:

    • Contact hypersensitivity (CHS) is a T cell-mediated immune response.
    • Aging is associated with altered immune function, including changes in hypersensitivity reactions.
    • The role of splenic T cells in age-related decline of CHS is not fully understood.

    Purpose of the Study:

    • To investigate the role of splenic T cells in the age-related suppression of contact hypersensitivity in mice.
    • To determine if splenic T cells from aged mice can suppress the induction or elicitation phases of CHS.

    Main Methods:

    • Adult thymectomized CBA mice were injected intravenously with spleen cells from intact CBA mice.
    • Contact hypersensitivity to picryl chloride was induced and elicited.

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  • The effect of spleen cell transfer on CHS was assessed, including inhibition by anti-Thy 1 serum and complement.
  • Spleen cells from donors pre-treated with picryl sulfonic acid were also tested.
  • Main Results:

    • Spleen cells from intact aged mice suppressed the elicitation phase of CHS.
    • This suppression was mediated by Thy 1-positive T cells.
    • The induction phase of CHS was not affected by these cells.
    • Spleen cells from picryl sulfonic acid-treated donors suppressed both induction and elicitation phases.

    Conclusions:

    • A splenic suppressor T cell population emerges with age in mice.
    • These suppressor T cells predominantly inhibit the elicitation phase of contact hypersensitivity.
    • This splenic suppressor T cell activity may explain the decline in CHS in aging mice.