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Specific unresponsiveness in nude mice given antigen before T cells
1Basel Institute for Immunology, 487, Grenzacherstr., CH-4058 Basel, Switzerland.
European Journal of Immunology
|September 1, 1975
Summary
This study shows that immune tolerance in mice can be reversed by treating spleen cells with lysed cell supernatant, suggesting a reversible B cell receptor blockade rather than T cell involvement.
Area of Science:
- Immunology
- Cellular immunology
- Immune tolerance
Background:
- Specific immune tolerance can be induced in nude mice by antigen exposure followed by congenic T cell administration.
- Recovery of immune responsiveness after induced tolerance typically requires at least two weeks.
Purpose of the Study:
- To investigate the mechanism underlying long-term immune tolerance induced by antigen and T cells in mice.
- To determine if the unresponsiveness is mediated by T cells or other immune components.
- To explore methods for reversing established immune tolerance.
Main Methods:
- Induction of specific tolerance in nude mice using antigen and congenic T cells.
- Transfer of spleen cells from tolerant mice to irradiated congenic recipients with normal thymocytes.
- Treatment of spleen cells with supernatant from lysed cells prior to transfer.
- Assessment of recipient responsiveness to the antigen post-transfer.
Main Results:
- Recipients of spleen cells from tolerant mice, along with normal thymocytes, typically remained unresponsive.
- Treatment of tolerant spleen cells with lysed cell supernatant restored responsiveness in transfer experiments.
- Spleen cells from unresponsive mice did not suppress normal spleen cells in transfer.
- Unresponsiveness was not reversed by the presence of allogeneic cells.
Conclusions:
- The findings suggest that the induced unresponsiveness is likely due to a reversible blockade of B cell receptors.
- The results indicate that T cells are not the primary mediators of this specific type of immune tolerance.
- This reversible B cell receptor blockade offers a potential target for modulating immune responses.