Immune Response and Vaccination
Phagocytes (neutrophils, macrophages) engulf pathogens; macrophages become antigen-presenting cells. T-helper cells with complementary receptors are activated and release cytokines. B cells with complementary receptors undergo clonal selection and expansion, forming plasma cells (secrete antibodies) and memory cells. Cytotoxic T cells kill infected cells. Antibodies: four polypeptide chains (2 heavy, 2 light), variable regions with two antigen-binding sites, held by disulfide bonds; cause agglutination, neutralisation and opsonisation. The secondary response is faster and larger because of memory cells. Active immunity (own antibodies; natural infection or vaccination) is long-lasting; passive (given antibodies; placenta, milk, injection) is short-term. Herd immunity protects the unvaccinated. Monoclonal antibodies target specific antigens for diagnosis and treatment.
Learning objectives
- Describe phagocytosis and antigen presentation.
- Describe B and T cell responses.
- Relate antibody structure to function.
- Compare types of immunity and explain vaccination.
Why do you usually catch chickenpox only once?
Core idea
Catch measles once and you're protected for life. Your immune system keeps a record.
Lymphocytes with complementary receptors are selected and cloned; memory cells make the next response faster and larger.
Humoral and cell-mediated responses.
Classify: (a) measles vaccine; (b) antibodies in breast milk.
- Goal
- Type.
- Strategy
- Made or given? Natural or artificial?
- Artificial active.
- Natural passive.
Summary
- Antigen presentation.
- Clonal selection.
- Antibodies: 4 chains, 2 binding sites.
- Active vs passive.
- Antigen
- Molecule that triggers an immune response.
- Memory cell
- Long-lived lymphocyte that gives a rapid secondary response.
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