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Updated: Jan 10, 2026

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Murine Model of Epicutaneously-Induced Immunomodulation
Published on: June 24, 2025
469
Modulation of help and suppression in a hapten-carrier system
Journal of Immunology (Baltimore, Md. : 1950)
|March 1, 1976
Summary
Beta-galactosidase (GZ) dose and timing determine immune response modulation. Early GZ priming induces suppression, while later priming enhances responses to trinitrophenyl-GZ (TNP-GZ) in mice.
Area of Science:
- Immunology
- Cellular immunology
- T cell regulation
Background:
- Beta-galactosidase (GZ) can modulate immune responses.
- Trinitrophenyl-GZ (TNP-GZ) is used to study immune reactions.
- CBA/J mice are a standard model for immunological studies.
Purpose of the Study:
- To investigate the dual role of beta-galactosidase (GZ) in modulating immune responses.
- To define conditions for GZ-induced immune help or suppression.
- To elucidate the T cell-mediated mechanisms underlying these effects.
Main Methods:
- Adoptive transfer of primed spleen cells into irradiated recipients.
- Immunization with varying doses and time points of GZ.
- Challenge with trinitrophenyl-GZ (TNP-GZ) conjugates.
- Analysis of anti-TNP antibody responses.
Main Results:
- GZ administration can either help or suppress subsequent anti-TNP responses.
- Optimal help observed with spleen cells from mice primed >9 days with low-dose GZ.
- Optimal suppression observed with spleen cells from mice primed 3 days with high-dose GZ.
- Both help and suppression are T cell-mediated and carrier-specific.
Conclusions:
- Immune response to TNP-GZ is regulated by a temporal wave of suppression followed by help.
- The dose and timing of GZ exposure critically determine the outcome.
- T cells play a central role in mediating both GZ-induced help and suppression.

