Level 2 — RecallImmune System

Immune System

30 minutes40 marksprintable — key stays hidden on paper

Level 2 (Recall & Understanding)

Time limit: 30 minutes
Total marks: 40


Instructions: Answer all questions. Marks are shown in brackets.


Q1. Define the following terms: (a) antigen, (b) antibody, (c) immunological memory. [3]

Q2. Distinguish between innate immunity and adaptive immunity by giving three points of difference. [3]

Q3. The skin and mucous membranes form the body's first line of defence. (a) Name two physical barriers to pathogen entry. [2] (b) Name two chemical barriers and state the role of each. [3]

Q4. Describe the inflammatory response. In your answer, name the chemical released by mast cells, and list three visible signs of inflammation. [5]

Q5. Describe the process of phagocytosis carried out by macrophages and neutrophils, in the correct sequence of steps. [4]

Q6. Distinguish between B cells and T cells with respect to: (a) site of maturation, (b) main function, (c) the type of immunity each is associated with. [3]

Q7. (a) Draw and label a simple diagram of an antibody (immunoglobulin) molecule, showing the heavy chains, light chains, antigen-binding sites, and variable/constant regions. [4] (b) State two functions of antibodies. [2]

Q8. Explain the role of MHC molecules in antigen presentation. Distinguish between MHC class I and MHC class II with respect to which cells display them and which T cells recognise them. [4]

Q9. Compare active immunity and passive immunity using the table headings: source of antibodies, speed of onset, and duration of protection. [4]

Q10. (a) Define a vaccine. [1] (b) Explain what is meant by herd immunity and state one reason it protects individuals who are not vaccinated. [2] (c) State one difference between an allergy and an autoimmune disorder. [2]


END OF PAPER

Answer keyMark scheme & solutions

Q1. [3] (1 mark each)

  • (a) Antigen — a foreign molecule (often a protein/glycoprotein on a pathogen surface) that is recognised by the immune system and triggers an immune response. (1)
  • (b) Antibody — a Y-shaped protein (immunoglobulin) produced by plasma (B) cells that binds specifically to an antigen. (1)
  • (c) Immunological memory — the ability of the adaptive immune system to respond faster and more strongly upon re-exposure to a previously encountered antigen, due to memory cells. (1)

Q2. [3] (1 mark per valid difference)

Innate Adaptive
Non-specific Specific to antigen
Rapid (present from birth) Slower on first exposure
No memory Has immunological memory
Barriers, phagocytes, inflammation B cells, T cells, antibodies
Any three contrasts = 3 marks.

Q3. [5]

  • (a) Physical barriers (any 2): intact skin/keratinised epidermis; mucous membranes/mucus; cilia; hairs. (1 each, max 2)
  • (b) Chemical barriers (any 2 with role): lysozyme in tears/saliva — kills bacteria by digesting cell walls; stomach acid (HCl, low pH) — kills ingested microbes; sebum/sweat (low pH, fatty acids) — inhibits microbial growth. (1 for barrier + role, ×… actually 1.5 each ≈ 3 total; award 3 for two correct barrier+role pairs.)

Q4. [5]

  • Tissue damage/infection → mast cells release histamine (1)
  • Histamine causes vasodilation of local blood vessels → increased blood flow (1)
  • Increased capillary permeability → plasma and phagocytes leak into tissue (1)
  • Phagocytes (neutrophils, macrophages) attracted to site (chemotaxis) (1)
  • Three signs: redness, heat, swelling (also pain) (1)

Q5. [4] (1 mark each, sequence)

  1. Chemotaxis / recognition — phagocyte attracted to and binds the pathogen (aided by opsonins). (1)
  2. Engulfment — cell membrane extends around pathogen, enclosing it in a phagosome (vesicle). (1)
  3. Fusion — phagosome fuses with a lysosome forming a phagolysosome. (1)
  4. Digestion — lysosomal enzymes (e.g. lysozyme) destroy the pathogen; debris is expelled/antigen presented. (1)

Q6. [3] (1 mark each)

  • (a) B cells mature in bone marrow; T cells mature in the thymus. (1)
  • (b) B cells produce antibodies; T cells kill infected cells / help & coordinate the response. (1)
  • (c) B cells → humoral immunity; T cells → cell-mediated immunity. (1)

Q7. [6]

  • (a) Diagram: Y-shaped molecule showing two heavy chains + two light chains joined by disulfide bonds; two antigen-binding sites at the tips; variable regions (at tips) and constant regions (stem/Fc). (4 — 1 per correctly shown/labelled feature)
  • (b) Functions (any 2): neutralisation of toxins/pathogens; agglutination (clumping); opsonisation (marking for phagocytosis); complement activation. (1 each, max 2)

Q8. [4]

  • MHC molecules are cell-surface proteins that display (present) antigen fragments to T cells. (1)
  • MHC class I — on all nucleated cells; presents intracellular (e.g. viral) antigens; recognised by cytotoxic T cells (CD8). (1.5)
  • MHC class II — on antigen-presenting cells (macrophages, dendritic cells, B cells); presents extracellular antigens; recognised by helper T cells (CD4). (1.5)

Q9. [4] (table, ~1.3 marks per row; full = 4)

Active immunity Passive immunity
Source of antibodies Made by own body Received ready-made
Speed of onset Slow (days–weeks) Immediate
Duration Long-lasting (memory cells) Short-lived (no memory)
(Award 4 for all three rows correct.)

Q10. [5]

  • (a) A vaccine is a preparation of weakened/inactivated pathogen or its antigens given to stimulate active immunity without causing disease. (1)
  • (b) Herd immunity — when a large proportion of a population is immune, transmission of the pathogen is greatly reduced. (1) Unvaccinated individuals are protected because there are too few susceptible hosts for the pathogen to spread. (1)
  • (c) Allergy = immune overreaction to a harmless foreign antigen (allergen); autoimmune disorder = immune system attacks the body's own (self) tissues. (2)
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