Immunological Tolerance

22 questions β€’ 1 test β€’ tap a section to begin

Welcome! 8.2 Immunological Tolerance β€” Test 1 — 22 questions, CSIR-NET style.

What this test covers

  • Central tolerance: deletion, AIRE, receptor editing
  • Peripheral tolerance: anergy, Tregs, deletion
  • Tolerance-favouring conditions; immune privilege
  • Sequestered antigens; failure β†’ autoimmunity

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8.2 Immunological Tolerance β€” Test 1
Q1. Immunological tolerance is best defined as:βœ“ Specific unresponsiveness to a particular antigen (especially self)
Q2. Central tolerance is established in the:βœ“ Primary lymphoid organs (thymus and bone marrow)
Q3. Negative selection in the thymus contributes to tolerance by:βœ“ Deleting strongly self-reactive T cells
Q4. Peripheral tolerance is needed because:βœ“ Some self-reactive lymphocytes escape central tolerance
Q5. Anergy as a tolerance mechanism arises when a lymphocyte:βœ“ Recognises antigen without adequate co-stimulation
Q6. Regulatory T (Treg) cells maintain tolerance by:βœ“ Actively suppressing other lymphocytes (via IL-10, TGF-Ξ², etc.)
Q7. The transcription factor required for regulatory T-cell development and function is:βœ“ FoxP3
Q8. Clonal deletion as a tolerance mechanism refers to:βœ“ Apoptosis of self-reactive lymphocytes
Q9. The transcription factor AIRE promotes central tolerance by:βœ“ Driving expression of peripheral self-antigens in the thymic medulla
Q10. Factors that favour tolerance rather than immunity to an antigen include:βœ“ Very high or very low antigen dose and lack of co-stimulation/danger signals
Q11. Receptor editing contributes to B-cell tolerance by:βœ“ Re-rearranging light-chain genes to change a self-reactive receptor
Q12. Failure of self-tolerance leads to:βœ“ Autoimmune disease
Q13. Immune privilege (e.g. in the eye and brain) helps maintain tolerance by:βœ“ Limiting immune responses at certain sites to protect vital tissue
Q14. Sequestered (hidden) self-antigens can break tolerance if:βœ“ Tissue injury exposes them to the immune system
Q15. Oral administration of antigen often induces:βœ“ Oral (mucosal) tolerance
Q16. CTLA-4 contributes to peripheral tolerance by:βœ“ Delivering inhibitory signals that limit T-cell activation
Q17. Neonatal exposure to an antigen (as in classic experiments) tends to induce:βœ“ Tolerance to that antigen
Q18. A key difference between central and peripheral tolerance is that central tolerance:βœ“ Acts during lymphocyte development in primary organs
Q19. Tolerance is antigen-specific, which distinguishes it from:βœ“ General immunosuppression (which is non-specific)
Q20. Self-reactive antibody levels are low in normal serum largely because:βœ“ Self-reactive B cells stimulated without T-cell help undergo functional silencing/apoptosis
Q21. Anergy refers to:βœ“ A state of functional unresponsiveness to antigen
Q22. Match each tolerance mechanism with its description and select the correct option.βœ“ A-ii, B-iv, C-i, D-iii