Unit 2 - Cell Recognition + The Immune System Flashcards

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1
Q

What is an antigen?

A

A foreign molecule that stimulates an immune response. They are often proteins or glycoproteins.

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2
Q

Definition of foreign?

A

In biology, foreign means something which is not part of the host organism (your own body).

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3
Q

Antigens enable the immune system to identify what cells and molecules?

A

-Pathogens
-Abnormal body cells, e.g. cancer cells + infected cells
-Toxins
-Cells from other individuals of the same species.

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4
Q

What are pathogens?

A

Pathogens are microorganisms that cause disease, e.g. bacteria, fungi + viruses.

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5
Q

How do pathogens cause disease?

A

By damaging/killing cells and tissues and producing toxins.

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6
Q

What are phagocytes?

A

White blood cells that carry out phagocytosis, which involves engulfing the foreign antigen.

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7
Q

What is the 1st stage of the immune response and why is it nonspecific?

A

Stage 1 = Phagocytosis.
It is nonspecific because phagocytes will engulf anything foreign.

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8
Q

Steps of phagocytosis?

A

1) Phagocyte recognises the antigen as foreign.
2) The pathogen is engulfed by the phagocyte.
3) Engulfed pathogen is contained inside a vesicle called a phagosome.
4) Lysosomes fuse with the phagosome releasing lysozymes into the phagosome.
5) Lysozyme enzymes hydrolyse the molecules, e.g. proteins in the pathogen.
6) The antigens from the pathogen are presented on the cell surface membrane of the phagocyte - the phagocyte becomes an antigen presenting cell.

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9
Q

Acronym to remember phagocytosis?

A

Phagocyte
Recognises foreign antigen
Engulfs antigen
Phagosome
Fuses (lysosome)
Enzymes (lysozymes)
Hydrolyse
Antigen presented
Membrane
Acronym=Penis Reaches Extreme Places for Extreme Happiness A-Men.

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10
Q

What is the 2nd stage of the immune response?

A

Specific immune response. It would take too long to destroy a pathogen using only just phagocytosis, so a specific response is initiated where a specific foreign antigen is targeted.

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11
Q

What are helper t-cells?

A

White blood cells that have protein receptors in their cell membrane.

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12
Q

How are t-cells activated?

A

Helper t-cell with specific complementary receptor, binds to antigen on antigen presenting cell and the t-cell is activated.

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13
Q

The activated t-cell then releases chemical signals (cytokines) which further activates what?

A

-More phagocytes.
-Cytotoxic t-cells which kill infected cells directly.
-Specific B-cells also a type of white blood cell.

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14
Q

What is part 1 of stage 2?

A

The cellular response - T cells.

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15
Q

Acronym for cellular response (t-cells)?

A

An antigen presenting cell
Activates
Specific
T-cell
Clones (mitosis)
Cytotoxic t-cells
Helper T cells
Stimulating
B-cells
Phagocytes
Acronym = An Awesome Shag Touches Clit Carefully He Should Be Proud

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16
Q

What is part 2 of stage 2?

A

Humoral response - B cells.

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17
Q

How are specific b cells activated?

A

By their specific helper T cell.

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18
Q

What is the humoral response?

A

1) Specific B cells are activated by their specific helper T cell.
2) B cells clone into memory cells and plasma cells.
3) Plasma cells secrete specific antibodies which bind the foreign antigen.

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19
Q

Acronym for the humoral response?

A

T helper cell (specific)
Activates
B cell (specific)
Clones by mitosis
Plasma cells
Antibodies
Memory cells
Acronym = To Activate Boner Chew Penis All Morning.

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20
Q

What do plasma cells release?

A

Many monoclonal antibodies which have binding sites complementary to the same antigen and bind, leading to the destruction of the pathogen through agglutination and phagocytosis.

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21
Q

Definition of monoclonal antibodies?

A

Antibodies with the same tertiary structure, which are complementary to and bind one type of antigen. They come from the same type of B cell.

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22
Q

What is the primary immune response?

A

Helper T cells activating B cells to result in antibody production. This occurs each time you come across a new antigen that you have not been exposed to before.

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23
Q

What is the secondary immune response?

A

Memory B cells have an antibody with the same tertiary structure, complementary to the same antigen as the parent B cell. So if re-infected with the same antigen, memory B cells with the complementary antibody:
-bind the antigen
-clone into plasma cells
-produce many more antibodies, more quickly to kill the foreign cell.

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24
Q

Structure of an antibody?

A
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25
Q

Describe the structure of an antibody?

A

They have a quaternary structure made up of 4 polypeptide chains, 2 heavy chains and 2 light chains, held together by disulphide bridges. It’s a protein!

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26
Q

What are the 2 regions in an antibody?

A

Constant region = has the same tertiary structure in all antibodies.
Variable region = contains the binding site for antigens and differs between antibodies making antibodies complementary to only one type of antigen.

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27
Q

When an antibody binds to an antigen it is known as?

A

An antigen-antibody complex.

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28
Q

What is agglutination?

A

Antigen-antibody complexes cause the foreign cells to clump together as each antibody has 2 binding sites, which can bind to 2 antigens at the same time on different cells. This allows many cells to be engulfed by a phagocyte in one go.

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29
Q

Summary of the immune response? (Use this to answer 5 mark questions on the primary immune response)

A

1) A phagocyte engulfs the pathogen, hydrolyses it and presents antigens on its surface membrane.
2) Specific helper T cell with a complementary receptor protein binds to the antigen.
3) This helper T cell binds to and activates a specific b cell.
4) The specific b cell clones by mitosis into plasma cells which make and secrete many antibodies with specific binding sites complementary to the antigen.
5) The antibodies agglutinate the antigens, which are destroyed by phagocytes.
6) Memory b cells with the complementary antibody remain and clone into plasma cells when presented with the same antigen, producing many more antibodies, faster.

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30
Q

Primary and secondary response graph?

A
31
Q

Why do symptoms occur in the primary response?

A

Because when the antigen infects the body for the first time antibodies are produced more slowly and there are less of them as it takes time for clonal selection (the process by which a specific b cell is stimulated to clone) to occur so symptoms occur.

32
Q

Why do symptoms not occur in the secondary response?

A

Clonal selection occurs more quickly (because phagocytosis, antigen presentation and helper T cell activation is not required) and the plasma cells produce many more antibodies at a faster rate so the infection is overcome before any symptoms can occur.

33
Q

Overall how do vaccines work?

A

By creating a primary response against an antigen so that memory b cells are formed with complementary antibodies to the antigen, without the symptoms of the pathogen itself.

34
Q

How do vaccines work?

A

1) vaccines contain antigens from the pathogen.
2) a phagocyte (macrophage) engulfs the antigen and presents it on its surface membrane.
3) a specific helper T cell with a complementary receptor protein binds to the antigen.
4) this helper T cell stimulates a specific b cell which divides by mitosis.
5) the b cells clone into plasma cells which produce and secrete many antibodies with specific binding sites complementary to the antigen. The antibodies agglutinate the antigen and destroy it.
6) memory b cells are produced so on a second exposure to the antigen more antibodies are produced more quickly, destroying the pathogen before symptoms are displayed.

35
Q

Why sometimes are booster vaccines given out?

A

To increase the number of memory cells over a long period of time.

36
Q

What is herd immunity?

A

If a majority of the population are vaccinated then most people cannot get the disease. Therefore, those who are not vaccinated are also protected as there are less people to transmit the disease.

37
Q

What are ethical issues with vaccines?

A

-Development and testing may involve use of animal and it may cause some pain/suffering to the animals and a large number may be used.
-Human testing. Volunteers used for testing may be put at risk.
-The vaccine may have side effects. The risk and severity of these side effects can vary between vaccines.
-People may not have the vaccine due to risk of side effects and instead rely on herd immunity for protection. Is this fair to those who have had the vaccine?
-Who should receive a new vaccine first?
-Should all people be forced to have the vaccine if it benefits society even if certain groups may not agree with the vaccinations?

38
Q

What is antigenic variability?

A

Due to mutations in the DNA of pathogens, the tertiary structure of the antigen protein can change shape.

39
Q

How does antigenic variability cause a secondary response to not occur?

A

If a pathogen, which has previously infected the body, is encountered again with a changed antigen, the antigen binding site of antibodies from the memory cells will not be complementary and a secondary response does not occur. The patient will have to carry out the primary response again and experience the symptoms again.

40
Q

How does antigenic variability cause vaccines to become ineffective?

A

The antibodies produced as a result of the vaccine are no longer complementary. A new vaccine needs to be made each time the antigen changes which takes time and is expensive.

41
Q

What is active immunity?

A

Following exposure to an antigen, specific memory B cells are made which produce antibodies against antigen.
Natural - immune after actually having the disease.
Artificial - immune after given vaccination.

42
Q

Advantages of active immunity?

A

Long term protection as memory cells are made.

43
Q

Disadvantages of active immunity?

A

-Artificial can only be given before getting the disease.
-Takes more time before immune, to make memory cells.
-Natural will get symptoms of the disease.

44
Q

What is passive immunity?

A

Antibodies against the antigen are put straight into the body, the immune system does not make the antibodies.
Natural - a baby receives antibodies from its mother’s milk.
Artificial - injected with antibodies made in a lab.

45
Q

Advantages of passive immunity?

A

-Can be given after exposure to antigen/pathogen.
-Works straight away.

46
Q

Disadvantages of passive immunity?

A

Does not last long as antibodies broken down, no memory cells are produced.

47
Q

How are monoclonal antibodies used in treating diseases, I.e. cancer?

A

-Cancer cells have unique antigens on their cell membrane which normal body cells do not have.
-Monoclonal antibodies, which have an anti-cancer drug attached, can be made complementary to the cancer cell antigen.
-The monoclonal antibodies bind only to the cancer cells, killing them, reducing the side effects of the drug as fewer healthy cells are damaged.

48
Q

What protein is found in the urine of pregnant women?

A

hCG - human chorionic gonadotropin

49
Q

How are monoclonal antibodies used in pregnancy tests?

A

-The test strip on the pregnancy tests contains an hCG monoclonal antibody with a coloured dye attached.
-Urine flows along the test strip and any hCG in the urine binds the monoclonal antibody.
-The hCG-antibody complexes then flow into the test area when there are fixed hCG antibodies.
-The hCG-antibody complexes with the dye bind the fixed hCG antibodies and build up on the test line concentrating the dye. This causes the coloured band to appear (positive result).
-If there is no hCG present then the hCG antibodies antibodies flow past the fixed hCG antibodies on the test line and bind to the fixed antibodies on the control line.
-The antibodies fixed to the control line are complementary to the hCG antibody, not the hCG itself.
-The colour of the test line changes, showing the test has worked correctly, but as there is only one coloured line, and not two, it is a negative result.

50
Q

How are monoclonal antibodies used to diagnose disease using tissue samples?

A

Monoclonal antibodies complementary to the antigens on cancer cells can be used in cancer diagnosis on biopsy tissue samples.
The antibody complementary for the cancer antigen has a fluorescent tag on it which shows up down a microscope.

51
Q

What is ELISA (Enzyme Linked ImmunoSorbant Assay)?

A

ELISA uses monoclonal antibodies to detect the presence of a certain antibody or antigen in the body. This is used to determine if an individual has a disease or not.

52
Q

Specific antigens indicate what?

A

The presence of a pathogen.

53
Q

Antibodies indicate the presence of what?

A

That the person has been exposed to the pathogen which has stimulated an immune response.

54
Q

Indirect ELISA is used to?

A

Detect an antibody.

55
Q

Direct ELISA is used to?

A

Detect the presence of antigens, instead of antibodies.

56
Q

Steps of the ELISA process?

A

1) The antigen is bound to the bottom of a plastic well.
2) A sample is added to the well. If any antibodies against the pathogen are present then the antibody binds to the antigen. Well is washed to remove any unbound antibodies.
3) A second antibody, complementary to the first antibody, is added. This antibody has an enzyme attached to it.
4) The well is washed again to remove any unbound enzyme-linked antibody. This is very important as this produces a negative result if no antibodies are present in the person’s sample. If it was not washed then a false positive would occur (there would be a colour change) as the enzyme is present.
5) A solution is added to the well which contains a substrate. The enzyme on the 2nd antibody reacts with the substrate, producing a colour change, which is a positive result for the presence of the antibody.

57
Q

What is HIV?

A

HIV = human immunodeficiency virus.
It’s a retrovirus which infects and kills helpers T-cells, reducing the effectiveness of the immune response.

58
Q

Structure of HIV?

A
59
Q

Attachment protein?

A

Attaches virus to complementary receptor on host helper T cell.

60
Q

RNA?

A

Genetic material of HIV.

61
Q

Reverse transcriptase?

A

Enzyme which converts RNA into DNA in host cell.

62
Q

Capsid?

A

Made of protein.

63
Q

Lipid envelope?

A

Outer layer made of membrane taken from previous host cell.

64
Q

Replication of HIV?

A

1) The attachment protein on HIV binds to a complementary receptor on the helper T-cell.
2) The capsid enters the cell and releases the RNA into the cytoplasm.
3) Reverse transcriptase makes DNA from the HIV RNA.
4) Using the host cells enzymes and ribosomes for protein synthesis, viral proteins are made from the DNA.
5) New virus particles are formed from the proteins which bud from the cell and infect more Helper T cells.

65
Q

A VIRUS has a CAPSID! PROKARYOTES have a CAPSULE!

A
66
Q

What does AIDS stand for?

A

Acquired Immune Deficiency Syndrome.

67
Q

What happens when helper T-cell numbers become very low?

A

The immune system starts to fail and serious infections can kill the patient.

68
Q

When is AIDS clinically diagnosed?

A

When the T cell number drops below 200 per ml of blood.

69
Q

What do antibiotics treat?

A

They only kill bacteria and not viruses.

70
Q

Why do antibiotics only kill bacteria?

A

Because they target parts of a bacteria which are not found in a virus, i.e. the bacterial cell wall, ribosomes and bacterial enzymes.

71
Q

Why are viruses difficult to kill?

A

Because they replicate inside cells and have very few drug targets such as enzymes, as they use the host cells’ enzymes and organelles for replication.

72
Q

What is one target for antiviral drugs?

A

The viral reverse transcriptase, but this only works if it’s a retrovirus (reverse transcriptase inhibitors) which contains the reverse transcriptase.

73
Q

Why do antibiotics not kill human cells?

A

Because bacterial enzymes and ribosomes (70s in bacteria and 80s in eukaryotic) are different in each.

74
Q

How can you prevent the spread of HIV?

A

-Protected sex.
-Using clean sterilised needles.
-HIV positive mothers take anti-retroviral drugs during pregnancy to reduce chance of giving baby HIV.