2.4 Cell recognition and the immune system Flashcards

1
Q

What is an antigen?

A

● Foreign protein
● That stimulates an immune response leading to production of antibody

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2
Q

How are cells identified by the immune system?

A

● 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

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3
Q

What types of cells and molecules can the immune system identify?

A

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

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4
Q

Describe phagocytosis of pathogens (non-specific immune response

A

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

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5
Q

Describe the response of T lymphocytes to a foreign antigen (the cellular
response)

A

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

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6
Q

Describe the response of B lymphocytes to a foreign antigen (the humoral
response)

A
  1. 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
  2. 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
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7
Q

What are antibodies?

A

● 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

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8
Q

Explain how antibodies lead to the destruction of pathogen

A

● 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

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9
Q

Explain the differences between the primary & secondary immune response

A

● 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

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10
Q

Explain how vaccines provide protection to individuals against disease

A

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

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11
Q

Explain how vaccines provide protections for populations against disease

A

● 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

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12
Q

What is a vaccine?

A

● Injection of antigens from dead or weakened pathogens
● Stimulating formation of memory cells

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13
Q

Describe the differences between active and passive immunity

A

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 (

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14
Q

Explain the effect of antigen variability on disease and disease prevention

A

● 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

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