Antigen Presentation

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

Welcome! 6.3 Antigen Presentation β€” Test 1 — 22 questions, CSIR-NET style.

What this test covers

  • Professional APCs & dendritic-cell maturation/migration
  • Co-stimulation (B7–CD28) & CTLA-4
  • Cross-presentation & the immunological synapse
  • Linked recognition, FDCs, CD1 lipid presentation

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6.3 Antigen Presentation β€” Test 1
Q1. The most potent professional antigen-presenting cell, able to prime naive T cells, is the:βœ“ Dendritic cell
Q2. The three professional antigen-presenting cell types are:βœ“ Dendritic cells, macrophages and B cells
Q3. Dendritic cells capture antigen in peripheral tissues and then:βœ“ Mature and migrate to lymph nodes to present to T cells
Q4. B cells are especially efficient at presenting antigen that:βœ“ They capture via their specific B-cell receptor
Q5. Co-stimulatory molecules B7-1/B7-2 (CD80/CD86) on a mature APC engage which receptor on the T cell?βœ“ CD28
Q6. Antigen presentation without adequate co-stimulation tends to induce:βœ“ T-cell anergy or tolerance
Q7. Cross-presentation by dendritic cells is important because it allows:βœ“ Priming of CD8 CTLs against antigens the DC did not synthesise
Q8. MHC class II expression on non-professional cells can be induced by:βœ“ IFN-Ξ³
Q9. The immunological synapse formed between a T cell and an APC functions to:βœ“ Organise receptors and signalling molecules for efficient activation
Q10. Linked recognition in T-dependent antibody responses means that:βœ“ The B cell and helper T cell recognise epitopes on the same antigen
Q11. A resting (immature) dendritic cell is specialised for:βœ“ Antigen capture rather than T-cell activation
Q12. CTLA-4 (CD152) on T cells differs from CD28 in that it:βœ“ Delivers an inhibitory signal, dampening T-cell activation
Q13. Superantigens cause excessive presentation-independent activation by:βœ“ Bridging MHC II and the TCR VΞ² region outside the peptide groove
Q14. Follicular dendritic cells (FDCs) in germinal centres differ from conventional dendritic cells in that they:βœ“ Display intact antigen–antibody complexes to B cells (not peptide to T cells)
Q15. The principal signal that licenses a dendritic cell to mature and upregulate co-stimulators is:βœ“ Recognition of PAMPs/DAMPs (e.g. via TLRs)
Q16. Why is co-stimulation an important safeguard?βœ“ It restricts full T-cell activation to contexts of genuine danger (infection)
Q17. Macrophages presenting antigen are particularly important for:βœ“ Reactivation of effector/memory T cells at sites of infection
Q18. A key reason dendritic cells, and not most other cells, prime naive T cells is that they:βœ“ Express high co-stimulation plus abundant MHC and migrate to T-cell zones
Q19. Presentation of lipid antigens (rather than peptides) to certain T cells is carried out by:βœ“ CD1 molecules
Q20. Which cells are professional antigen-presenting cells?βœ“ Dendritic cells
Q21. A helper T cell with CD4 interacts with:βœ“ A class II MHC–antigen complex
Q22. Match each cell/molecule with its role in presentation and select the correct option.βœ“ A-ii, B-iv, C-i, D-iii