2.4 Cell recognition and the immune system Flashcards
What is an antigen?
● Foreign protein
● That stimulates an immune response leading to production of antibody
How are cells identified by the immune system?
● Each type of cell has specific molecules on its surface (cell-surface membrane / cell wall) that identify it
● Often proteins → have a specific tertiary structure
What types of cells and molecules can the immune system identify?
Pathogens (disease causing microorganisms) eg. viruses, fungi, bacteria
Cells from other organisms of the same species (eg. organ transplants)
Abnormal body cells eg. tumour cells or virus-infected cells
Toxins (poisons) released by some bacteria
Describe phagocytosis of pathogens (non-specific immune response
1 Phagocyte recognises foreign antigens on pathogen
2 Phagocyte engulfs pathogen by surrounding it with its cell membrane forming a phagosome vesicle
3 Pathogen contained in phagosome vesicle in cytoplasm
4 Lysosome fuses with phagosome and releases lysozymes (hydrolytic enzymes)
5 Lysozymes hydrolyse / digest pathogen
Describe the response of T lymphocytes to a foreign antigen (the cellular
response)
Specific helper T cells with complementary receptors (on cell surface) bind to antigen on antigen-presenting cell → activated and divide by mitosis to form clones which stimulate:
● Cytotoxic T cells → kill infected cells / tumour cells (by producing perforin)
● Specific B cells (humoral response - see below)
● Phagocytes → engulf pathogens by phagocytosis
Describe the response of B lymphocytes to a foreign antigen (the humoral
response)
- Clonal selection:
○ Specific B lymphocyte with complementary receptor (antibody on cell surface) binds to antigen
○ This is then stimulated by helper T cells (which releases cytokines)
○ So divides (rapidly) by mitosis to form clones - Some differentiate into B plasma cells → secrete large amounts of monoclonal antibody
3.Some differentiate into B memory cells → remain in blood for secondary immune response
What are antibodies?
● Quaternary structure proteins (4 polypeptide chains)
● Secreted by B lymphocytes eg. plasma cells in response to specific antigens
● Bind specifically to antigens forming antigen-antibody complexes
Explain how antibodies lead to the destruction of pathogen
● Antibodies bind to antigens on pathogens forming an antigen-antibody complex
○ Specific tertiary structure so binding site / variable region binds to complementary antigen
● Each antibody binds to 2 pathogens at a time causing agglutination (clumping) of pathogens
● Antibodies attract phagocytes
● Phagocytes bind to the antibodies and phagocytose many pathogens at once
Explain the differences between the primary & secondary immune response
● Primary- first exposure to antigen
○ Antibodies produced slowly & at a lower conc.
○ Takes time for specific B plasma cells to be
stimulated to produce specific antibodies
○ Memory cells produced
● Secondary- second exposure to antigen
○ Antibodies produced faster & at a higher conc.
○ B memory cells rapidly undergo mitosis to
produce many plasma cells which produce
specific antibodies
Explain how vaccines provide protection to individuals against disease
Specific B lymphocyte with complementary receptor binds to antigen
Specific T helper cell binds to antigen-presenting cell and stimulates B cell
B lymphocyte divides by mitosis to form clones
Some differentiate into B plasma cells which release antibodies
Some differentiate into B memory cells
On secondary exposure to antigen, B memory cells rapidly divide by mitosis to produce B plasma cells
These release antibodies faster and at a higher concentration
Explain how vaccines provide protections for populations against disease
● Herd immunity- large proportion of population vaccinated, reducing spread of pathogen
○ Large proportion of population immune so do not become ill from infection
○ Fewer infected people to pass pathogen on / unvaccinated people less likely to come in contact
with someone with disease
What is a vaccine?
● Injection of antigens from dead or weakened pathogens
● Stimulating formation of memory cells
Describe the differences between active and passive immunity
Active immunity:
-requires exposure to antigen
-memory cells involved
-takes longer to develop
-Long term immunity as antibody can be produce
Passive immunity:
-no exposure to antigen
-no memory cells involved
Faster acting
Short term immunity as
antibody hydrolysed (
Explain the effect of antigen variability on disease and disease prevention
● Antigens on pathogens change shape / tertiary structure due to gene mutations (creating new strains)
● So no longer immune (from vaccine or prior infection)
○ B memory cell receptors cannot bind to / recognise changed antigen on secondary exposure
○ Specific antibodies not complementary / cannot bind to changed antigen