Immunological Tolerance Flashcards
Tolerance:
Lack of an immune response when immune cells are exposed to antigen.
Central tolerance:
Elimination of self reactive T and B cells during development in the thymus or bone marrow.
Peripheral tolerance:
Mechanisms after the lymphocyte has left bone marrow or thymus and encounters self antigen.
When T cells show a high affinity for self-antigen in the thymus (2):
- Deleted by apoptosis.
2. Survive and become regulatory T cells.
Transcription factor that regulates the expression of peripheral proteins in thymic tissue:
AIRE
- Autoimmune regulatory gene.
AIRE (3):
- Encodes a transcription factor that is expressed in the thymic medulla.
- Controls the expression of the thymic tissue restriction antigens.
- When defective –> autoimmunity.
Regulatory T cells (4):
- Most are CD4 T cells.
- Inhibit the activation of conventional CD4 and CD8 T cells and thus can prevent autoimmune and allergic disease.
- Produce IL-10 and CTLA-4.
- Express CD25 and transcription factor Foxp3.
When a self reactive T cell in the periphery encounters its self antigen it (3):
- Anergy.
- Deletion through apoptosis.
- Suppression by T regulatory cells.
Anergy:
A state of immune unresponsiveness after antigen encounter.
- Absent co-stimulation.
- CTLA-4 binds and blocks B7 on the APC and delivers inhibitory signals to the T cell.
CTLA-4:
Always expressed on Treg cells and is expressed on cytotoxic T cells after their activation, serving as an “off switch”.
- Has higher affinity for B7 than CD28.
Suppression by Tregs (4):
- Grow in response to IL-2.
- Produce cytokines IL-10 and TGF-beta.
- Express CTLA-4.
- Consume IL-2 so that is unavailable for effector T cells.
When developing B cells encounter self antigen in the bone marrow (2):
- Edit receptors.
2. Deletion through apoptosis.
B cell receptor editing (3):
- Reactivate RAG genes.
- Resume Ig light chain recombination and make new light chain.
- Same heavy chain is expressed.