2.3 (5) - Cells Recognition and the Immune System Flashcards

Defence mechanisms Phagocytosis T lymphocytes and cell-mediated immunity B lymphocytes and humoral immunity Antibodies Vaccination HIV

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1
Q

What is an antigen?

A

Any part of an organism (often a protein on a cell’s surface) that is recognised as foreign by our immune system

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2
Q

What can our immune system identify by its antigens?

A
  • Pathogens
  • Cells from other organisms of the same species
  • Cancerous cells
  • Toxins
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3
Q

Why are transplant organs often take from relatives?

A

Antigens are genetically controlled - close relatives have more similar antigens

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4
Q

What are the 2 types of immune systems?

A

Specific and non-specific

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5
Q

Describe a non-specific immune system

A
  • Response is immediate and the same for all pathogens
  • In all animals
  • Carries out phagocytosis, using phagocytes
  • Physical barriers
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6
Q

Describe a specific immune system

A
  • Only in vertebrates
  • Response is slower and specific to each pathogen
  • Cell-mediated response, using T lymphocytes
  • Humoral response, using B lymphocytes
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7
Q

What are some physical barriers to infection?

A
  • Skin - physical barrier that pathogens find difficult to penetrate
  • Epithelial cells in airways
  • Mucus - epithelial layers inside the body produce mucus that pathogens stick to, which immobilises them
  • Stomach acid - denatures enzymes or coats proteins of most pathogens that enter the stomach
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8
Q

Describe the 5 stages of phagocytosis

A

1) Pathogen gives off chemicals, so the phagocyte is attracted towards it PHAGOCYTE DETECTS AND MOVES TOWARDS CHEMICALS RELEASED FROM THE PATHOGEN ALONG A CONCENTRATION GRADIENT
2) Pathogen attaches to the phagocyte
3) The phagocyte engulfs the pathogen. It migrates to the phagosome in a vesicle
4) Lysozyme hydrolyses (break down) the pathogens in the phagosome
5) The phagocyte absorbs the products of hydrolysis

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9
Q

What are T lymphocytes?

A
  • Required for cell-mediated immunity
  • Have receptor proteins that, on each cell, can detect one specific antigen
  • Occur in 2 forms:
    1) Helper T-cells
    2) Cytotoxic T-cells
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10
Q

Describe the cell-mediated response in 5 stages

A

1) Pathogens invade cells OR are taken in by phagocytes
2) The phagocyte places antigens from the pathogen on its cell membrane
3) Receptors on a specific helper T cell fix exactly onto these antigens
4) This attachment activates the T cell to divide rapidly my mitosis and form a clone of genetically-identical cells

5) The activated, cloned T-cells can:
- divide by mitosis to produce helper-T cell clones (memory cells)
- release cytokines, to activate cytotoxic-T cells
- activate B cells to produce antibodies
- stimulate phagocytosis

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11
Q

What do cytotoxic T cells do?

A
  • Produce perforin (protein)
  • Makes holes in cell-surface membrane
  • Results in cell death
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12
Q

What are B lymphocytes?

A
  • Required for humoral immunity

- Display and secrete antibodies that can detect antigens and form antigen-antibody complexes

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13
Q

Describe the humoral response in 7 stages

A

1) The surface antigens of an invading pathogen are taken up by a B-cell
2) The B-cell processes the antigens and presents them on its surface
3) Helper T-cells attach to the processed antigens on the B-cell, activating the B-cell
4) The B-cell is now activated to divide by mitosis to give a clone of plasma cells
5) The cloned plasma cells produce and secrete the specific antibody that exactly fits the antigen on the pathogen’s surface

6) The antibody attaches to antigens on the pathogens and stops disease by:
- sticking cells together in large clumps (agglutination) and targeting them for destruction by phagocytosis
- preventing viruses and bacteria from infecting cells
- binding to free toxin proteins

7) Some B-cells develop into memory cells. These can respond to future infections by the same pathogen by dividing rapidly and developing into plasma cells that produce antibodies (secondary immune response)

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14
Q

What are antibodies made up of?

A

4 polypeptide chains

  • 2 heavy chains
  • 2 light chains
  • Joined by disulfide bonds
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15
Q

Describe an antibody’s shape

A

Form a Y-shaped structure

  • The stem = constant region
  • The ends of the arms = variable regions that bind to the antigen
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16
Q

What are monoclonal antibodies?

A
  • Antibodies produced from a single group of genetically-identical B-cells (or plasma cells) specific to 1 type of antigen
  • They are all identical in structure because:
    1) they have the same primary structure, as they are coded for by the same genes
    2) so, they have the same secondary and tertiary structures, because of being coded for by the same genes
17
Q

How are monoclonal antibodies used in cancer treatment?

A
  • Cancer cells have tumour markers
  • Monoclonal antibodies can be produced to bind to these tumour markers. Anti-cancer drugs can be attached to the antibodies
  • Therefore, the drugs will only be released where antibody binding occurs (ie, at cancer cells)
  • This importantly reduces side effects because the drugs will only accumulate at specific cells
18
Q

Describe how monoclonal antibodies are used in pregnancy tests

A
  • The placenta in a pregnant woman produces hCG. Can be found in the mother’s urine
  • Monoclonal antibodies are immobilised in coloured beads on a test strip
  • When urine is applied, the hCG will bind to the antibodies to form antigen-antibody complexes
  • The hCG-antibody-colour complex moves along the strip until it is trapped by a different type of antibody. The complexes accumulate to produce a coloured line to confirm pregnancy
19
Q

What are some ethical issues with using monoclonal antibodies?

A
  • Production involves mice to produce monoclonal antibodies, but to do this, they need to produce tumour cells
  • Negative results involved deaths in treating multiple sclerosis
20
Q

What is the primary immune response?

A
  • Happens when a new pathogen first invades
  • Relatively few initial specific T and B-cells
  • Because we start with less T and B-cells, relatively few clones are produced
  • Disease’s symptoms become visible
  • Once primary infection has been detected and responded to the person, they has become ‘immune’
21
Q

What are memory cells?

A
  • Some of the B and helper T-cells differentiate into memory cells
  • They remain in the blood for a number of years, so they can keep responding to pathogens
22
Q

What is the secondary immune response?

A
  • Happens when the same pathogen infects for a second time
  • Memory cells are present and ready to respond to a second infection (weeks, months or years later)
  • Much faster response to re-infection:
  • Memory T-cells divide into cytotoxic T-cells
  • Memory B-cells divide into plasma cells
  • Many more T and B-cells produced, therefore there is a much stronger response
  • Pathogens are destroyed before it can cause symptoms
23
Q

What is active immunity?

A
  • AKA vaccination
  • Vaccines contain dead/weakened pathogens
  • They do not cause disease but they do contain the antigens necessary to evoke a primary immune response
  • If the person later becomes infected by the live pathogen, the secondary response will occur
24
Q

What is passive immunity?

A
  • Occurs naturally (immunity passed from mother → baby)
  • And artificially (injecting antibodies):
  • Used when someone has already been infected (or is likely to become infected) with a pathogen
  • Antibodies extracted from blood plasma of an infected person
  • The antibodies assist the body’s normal immune response
  • Does not itself lead to long-term immunity
25
Q

Describe herd immunity

A
  • If enough people are immune to a pathogen (>90%), the remaining people are often protected
  • This is due to a lack of hosts for the pathogen to reproduce in
26
Q

What is antigenic variability?

A
  • Some pathogens have antigens that are constant, so we remain immune to them
  • Other pathogens develop new ‘strains’, with different antigens, so our bodies don’t have the memory cells against them
  • This can be caused by mutations or the horizontal transfer of plasmids, which contain new genes.
  • Infection by new ‘strain’ means that the primary response is needed to detect and respond to the infection
27
Q

What are the 6 components of HIV?

A
  • Attachment proteins
  • Lipid envelope
  • Capsid
  • Matrix
  • RNA
  • Reverse transcriptase
28
Q

What is the role of attachment proteins in a virus?

A

Attach to a host cell

29
Q

What is the role of the lipid envelope in a virus?

A

Derived from the host cell’s membrane, so that it becomes undetectable as a virus

30
Q

What is the role of the capsid in a virus?

A

Protein layer that encloses HIV’s RNA

31
Q

What is the role of the matrix in a virus?

A

Protein layer

32
Q

What is the role of the RNA in a virus?

A

Codes for viral proteins for viral replication

33
Q

What is the role of reverse transcriptase in a virus?

A

Enzyme for replication (RNA → DNA)

34
Q

Describe the process of HIV replication

A

1) HIV particles circulate around the bloodstream
2) HIV binds to CD4 glycoprotein of helper T cells (CD4).
3) HIV’s capsid fuses with Th’s cell membrane - releases capsid - it uncoats and releases RNA and reverse transcriptase into Th’s cytoplasm
4) Reverse transcription - RT converts viral RNA into DNA (it can do this because it’s a retrovirus).
5) DNA integrates into the Th cell’s nucleus, DNA is inserted into the host cell’s DNA.
6) Host turns viral DNA into mRNA, mRNA moves out of the Th’s nucleus via a nuclear pore.
7) The mRNA uses the Th cell’s protein synthesis mechanisms to make new HIV particles.
8) New virus particles break away from the Th cell with a bit of its cell membrane, which forms the HIV particle’s lipid envelope.

35
Q

What is AIDS?

A

HIV kills/interferes with normal functioning of the immune system, leading to AIDS.

36
Q

What does ELISA stand for?

A

Enzyme Linked Immunosorbent Assay

37
Q

Describe the ELISA test for HIV and AIDS

A
  • It uses antibodies to detect the presence and quality of a protein (antigen).
  • Very sensitive, so it can detect the smallest amounts of protein.
  • Can be used to detect hepatitis and tuberculosis.
  • Can also be useful for detect the amount of drugs in a person.
38
Q

What don’t antibiotics work on viruses?

A
  • There are no metabolic processes or cell structures for antibiotics to disrupt.
  • Working within our own body cells - hard for antibiotics to find viruses.
  • Viral protein coat means that antibiotics can’t bind to sites.