3.2.4- Cell Recognition- Immunity & Response Flashcards

1
Q

non-specific barriers

A

prevent pathogens from getting in- immediate and works for most pathogens

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2
Q

specific barriers

A

immune response to kill pathogens- slower and pathogen specific

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3
Q

non-specific barrier examples

A

skin, stomach, eyes, breathing system- physical barrier or phagocytes

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4
Q

specific barrier examples

A

Immune system: white blood cells, antitoxins, memory lymphocytes. Cell mediated or humoral response

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5
Q

Pathogen

A

A microorganism that causes disease

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6
Q

Infection

A

interaction or invasion of the body by a pathogenic organism. Cannot be killed by medication

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7
Q

immunity

A

the ability of an organism to resist a particular infection or toxin by the action of specific antibodies or sensitized white blood cells.

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8
Q

2 options upon infection

A
  1. pathogen overwhelms defences-> death
  2. defences overwhelm the pathogen->recovery
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9
Q

What must lymphocytes be able to do?

A

distinguish between self and non-self cells

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10
Q

what would happen if lymphocytes were unable to distinguish between self and non-self?

A

our immune system wouldn’t combat pathogens and would destroy our own tissues

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11
Q

how can lymphocytes distinguish between pathogens and self-cells?

A

markers are present on cell surfaces

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12
Q

antigen

A

molecule on the surface of pathogens that triggers an immune response.

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13
Q

clonal selection

A

antigens bind to specific receptors, causing a fraction of lymphocytes to clone themselves

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14
Q

Why do we not want lymphocytes to be complementary to self cells?

A

Because the lymphocytes would attack self cells and leave our immune system weak

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15
Q

Lymphocyte production in adults

A

In the bone marrow

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16
Q

Apoptosis

A

programmed cell death

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17
Q

How does cell recognition impact transplant patients?

A

The organ may often get rejected as the lymphocytes see it as a non-self cell. This causes the person to be very ill due to the strong immune response so they have to take immunosuppressant drugs.

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18
Q

Immunosuppressant drugs

A

drugs which suppress the immune system of the recipient of a transplanted organ to prevent rejection

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19
Q

White blood cells

A

fight infection and combat pathogens

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20
Q

Types of WBC

A

Lymphocytes and Phagocytes

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21
Q

Phagocytes

A

White blood cells that attack invading pathogens, non-specific and travel in blood but can move out to other cells due to segmented nucleus

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22
Q

Phagocytosis

A

Process in which a pathogen is engulfed

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23
Q

Phagocytosis step 1

A

Pathogen releases chemoattractants and the phagocyte is attracted to them so moves towards the pathogen.

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24
Q

Phagocytosis step 2

A

Receptors on the phagocyte attach to chemicals on the pathogen surface.

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25
chemoattractants
chemical signals and products of a pathogen
26
Phagocytosis step 3
formation of phagosome because the bacteria is engulfed. Lysosomes move closer to the phagosome
27
Phagocytosis step 4
Lysosomes fuse with the phagosome, and they release lysozymes (lytic enzymes) into the phagosome which hydrolyses the bacterium.
28
Phagocytosis step 5
The hydrolysis products of the bacterium are absorbed by the phagocyte. Antigens are presented on cell membrane of phagocyte
29
Purpose of presenting bacterium products
signals other areas of the immune system that there is an infection that they must fight & also they can produce antibodies.
30
Impact of pH change on immune response
could alter charges on the active site which break down pathogens so this could prevent pathogen hydrolysis.
31
What is a specific response?
A slower response that is specific to each pathogen
32
Advantage of specific response
Develops immunity in the long term
33
Disadvantage of specific response
Slower as it targets certain pathogens
34
Which cells are required to initiate a specific response?
Requires lymphocytes
35
T lymphocytes
cell-mediated immunity Mature in thymus gland
36
What do t lymphocytes respond to?
Responds to foreign material inside body cells so it only responds if pathogen is directly affecting body cells
37
Antigen presenting cells
Cells that display foreign antigens on their surface
38
T cells and phagocytes
When phagocytosis occurs, the pathogen is engulfed by a phagocyte and displays antigens. This means the T cells can bind
39
T cells and body cells invaded by viruses
They would display the antigens of the virus to alert the body to the virus invasion. Acts as a distress signal
40
T cells and cancer cells
They are different from healthy cells as they present antigens on the surface
41
T cells and transplanted cells
These are bodily cells but look completely different because they come from elsewhere so they contain different antigens
42
cell mediated immunity stage 1
pathogen invades body cells/taken in by phagocytes or engulfed
43
cell mediated immunity stage 2
phagocyte presents pathogen's antigens on it's cell surface membrane
44
cell mediated immunity stage 3
receptors on specific helper T cells fit exactly onto antigens because they are complementary
45
cell mediated immunity stage 4
activates the T cell to undergo clonal selection (divide through mitosis)
46
4 things cloned T cells can do
develop into memory cells stimulate the phagocytes stimulate the B cells to divide activate cytotoxic t cells
47
Cytotoxic T cells
attack abnormal body cells. Produce a protein called perforin that makes holes in the cell surface membrane and make it a freely permeable membrane
48
Perforin
One of the proteins released by cytotoxic T cells on contact with their target cells. It forms pores in the target cell membrane that contribute to cell killing.
49
B lymphocytes
form in the bone marrow and release antibodies that fight bacterial infections, respond to foreign material outside body cells
50
How do T and B cells work together?
B cells find an antigen in the body and join with it to form an antigen-antibody complex. It is taken up through endocytosis. B cells present the antigens on the surface and the T cells attach to B cells and help B to divide in clonal selection.
51
What happens in the second part of humoural immunity?
cloned B plasma cells produce specific antibodies for a quick response and they attach to the antigen of the pathogen and destroy it (primary response)
52
Humoural immunity
The type of response which involves B lymphocytes and antibodies.
53
what happens in the third stage of humoural immunity?
some B cells remain and become memory cells. They respond in the future and create the secondary response
54
Plasma cells
secrete antibodies into blood plasma but survive for only a few days. Part of primary response
55
Memory cells
live for decades, circulate in blood and tissue fluids. dont produce antibodies directly - divide into both plasma and memory cells for secondary response
56
Secondary immune response
memory cells facilitate a faster, more efficient response
57
Issues with memory cells?
Many pathogens have many cell surface proteins which acts as antigens and they can change and mutate meaning memory cells may not always recognise cells
58
Antigen variation
changing its appearance by altering surface antigens
59
antibodies
Specialized proteins that aid in destroying infectious agents
60
Where are antibodies found?
plasma cells
61
Describe the structure of an antibody in terms of protein hierarchy
They have a quaternary structure (3d shape and formed of many polypeptide chains). Two heavy polypeptide chains bonded to two light chains.
62
variable region of antibody
antigen binding site
63
constant region of antibody
terminal that contains 2 heavy chains; binds to receptors on cells
64
Explain why the Antibody will only detect a certain antigen (3 marks)
Antibody and it's variable region has a specific amino acid sequence This gives a specific shape (tertiary structure) which is complementary to the antigens It forms a complex between antigen and antibody
65
Do antibodies directly destroy antigens?
No they lead to antigen structure through other means
66
Agglutination
Clumping of microorganisms or blood cells, typically due to an antigen-antibody interaction. Easier for phagocytes to locate and engulf as they are less spread out
67
Markers (roles of antibodies)
Antibodies act as markers that stimulate phagocytes making it easier to engulf the pathogen
68
Monoclonal antibodies
Antibodies produced by a single clone of B lymphocytes and that are therefore identical in structure and antigen specificity. Single type. Often produced outside the body
69
Polyclonal antibodies
a series of antibodies are produced responding to a variety of different sites on the antigen. Produced from a variety of B cells
70
Monoclonal antibody therapy
A type of treatment by which monoclonal antibodies are administered, the antibodies form an antibody-antigen complex with cancerous cells which prevents further growth and stimulates chemical destruction of the cancer
71
Herceptin
Antibody for treating: Ovarian Cancer Breast cancer
72
What can Herceptin do?
Engulf cancer cells and mark them for destruction Block the chemical signals that stimulate uncontrolled growth
73
Advantages of antibody therapy
Non-toxic Highly specific
74
Indirect monoclonal antibody therapy
- a radioactive or cytotoxic drug is attached to a monoclonal antibody that is bound to antigens Kills cancer cells
75
How do pregnancy tests work?
1) Monoclonal antibodies are used to detect human chorionic gonadotropin (hCG) found in the urine of a pregnant woman 2) When urine is applied to the application area, the antibodies bind to any hCG, forming antigen-antibody complexes - these antibodies are attached to blue-coloured beads 3) The urine moves up to the test strip, where immobilised antibodies bind to any hCG antigen-antibody complexes - the test strip turns blue from the concentration of coloured beads
76
What can antibodies identify?
Flu, hepatitis, cancer, chlamydia
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ELISA test
Enzyme Linked Immunosorbent Assay uses antibodies to detect presence and quantity of a protein in a sample
78
1st stage of ELISA test
Apply sample to well surface. Antigens in sample attach to surface Wash to remove any unattached antigens
79
2nd stage of ELISA test
Add the antibody that is specific to the antigen we wish to detect. Leave to allow binding then wash.
80
3rd stage of ELISA test
Add a second antibody to bind with the 1st. This one will have an enzyme attached to it. Wash again.
81
4th stage of ELISA test
Add substrate to enzyme (must be colourless) This enzyme acts on substrate and causes a colour change for a positive result
82
ELISA positive result
Colour change
83
Ethical implications of monoclonal antibodies
Mice are used to test- animal cruelty Deaths associated with use of monoclonal antibodies Drug testing can impact even healthy people
84
Passive immunity
the short-term immunity that results from the introduction of antibodies from an outside source. No memory cells produced so it is short term but immediate.
85
Active immunity
production of antibodies stimulated by the individual. Requires direct contact with pathogen and takes time. Has 2 forms.
86
natural active immunity
production of one's own antibodies or T cells as a result of infection or natural exposure to antigen
87
artificial active immunity
Production of one's own antibodies or T cells as a result of vaccination against disease
88
Vaccines
A preparation that prevents a person from contracting a specific disease- contain small amounts of weakened or dead forms of a pathogen
89
When a vaccine is given to a person, it leads to the production of antibodies against a disease-causing organism. Describe how.
1. Vaccine contains antigen from pathogen;2. Macrophage presents antigen on its surface;3. T cell with complementary receptor protein binds to antigen;4. T cell stimulates B cell;5. (With) complementary antibody on its surface;6. B cell secretes large amounts of antibody;7. B cell divides to form clone all secreting / producing same antibody
90
Corona Virus vaccine
Developed a synthetic version of some of the virus' mRNA. Our cells read it as an instruction to start building spike proteins (antigens). The body then ammounts an immune response against them
91
How do you make a vaccination programme successful?
Cheap Few side effects Be able to produce, store and transport vaccines Administer them correctly
92
Herd immunity
The resistance of a group to an attack by a disease to which a large proportion of the members of the group are immune
93
How do you achieve herd immunity?
Vaccinate large amounts of a population all at the same time
94
Why are vaccination programs rarely 100% successful?
Some people have defected immune systems Pathogens can mutate and change their antigens Pathogens have different strains Some hide from immune systems People object to vaccinations
95
Ethics of vaccinations
Production uses animals Side effects Who should be tested on? Can people be forced to get a vaccine? Should expensive vaccination programmes still continue if a disease is eradicated?
96
Ethics of vaccinations
Production uses animals Side effects Who should be tested on? Can people be forced to get a vaccine? Should expensive vaccination programmes still continue if a disease is eradicated?