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Transfer of experimental autoimmune thyroiditis with T cell clones
Journal of Immunology (Baltimore, Md. : 1950)
|February 15, 1987
Summary
Three T lymphocyte clones were studied for their role in inducing thyroiditis. Clones A7 and B7 transferred thyroiditis to irradiated mice, with distinct cellular infiltrates and transient disease duration, highlighting T cell involvement in autoimmune thyroid disease.
Area of Science:
- Immunology
- Autoimmunity
- Thyroid Research
Background:
- T lymphocyte clones were isolated from CBA/CaJ mice immunized with mouse thyroid extract (MTE).
- Characterization of T cell clones involved in autoimmune responses is crucial for understanding disease pathogenesis.
Purpose of the Study:
- To investigate the ability of specific T lymphocyte clones to induce experimental thyroiditis.
- To analyze the characteristics of thyroid lesions and T cell helper functions associated with thyroiditis induction.
Main Methods:
- Isolation and characterization of T lymphocyte clones (L3T4+, Ig-, Lyt2-).
- Transfer of T cell clones to irradiated syngeneic mice to assess thyroiditis induction.
- In vitro assessment of T cell helper activity using B cell proliferation assays.
- Histological examination of thyroid tissues post-transfer.
Main Results:
- Clones A7 and B7 transferred transient thyroiditis to irradiated mice, characterized by mononuclear and/or polymorphonuclear cell infiltration.
- Clone B7 exhibited T cell helper activity for B cells when stimulated with trinitrophenyl-mouse thyroglobulin (MTG).
- Clone A7 induced mononuclear cell infiltration without significant helper activity, while clone D2 proliferated to MTG but did not transfer thyroiditis.
Conclusions:
- Specific T lymphocyte clones can transfer experimental autoimmune thyroiditis to susceptible hosts.
- The ability to induce thyroiditis and T cell helper functions are distinct properties of T cell clones.
- Loss of Thy marker on clone B7 did not affect its ability to transfer thyroiditis, suggesting complex regulatory mechanisms in autoimmune responses.