cell recognition and immunity Flashcards

1
Q

what can our immune system identify by their organisms

A

-pathogens
-cell surface structures
-cellls from other organisms of the same species
-cancerous cells
-toxins

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2
Q

main defence mechanisms of the body

A

non specific and specific

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3
Q

non specific response

A

response is immediate and the same for all pathogens

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4
Q

specific response

A

response is slower and specific to each pathogen

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5
Q

non specific response methods

A

primary method eg skin
secondary methods eg phagocytosis

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6
Q

specific response methods

A

-cell mediate response - t lymphocytes
humoral response - b lymphocytes

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7
Q

two immune system

A

non specific - all animals
specific-only vertebrates

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8
Q

what iOS the immune system

A

complex networks of cells tissue and organs and molecules

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9
Q

cells of immune system

A

white blood cells

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10
Q

inflammation

A

1)injury cut or graze
2)damaged white blood cells and mast cells from connective tissue releases histamines
3)dilation of arterioles in the area
4)increases blood flow in capillaries and capillary cells separate slightly
5)plasma white blood cells and antibodies leak into tissues causing oedema
6)white blood cells can destroy microbes

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11
Q

phagocytosis

A

1)neutrophils arrive first and engulf 5-20 bacteria but then die
2)macrophages arrive and destroy up to 100 bacteria

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12
Q

phagocytosis stages

A

1)chemotaxis
2)Adhesion
3)ingestion and intracellular digestion
4)disposal

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13
Q

chemotaxis

A

actively seek foreign antigens stimulated by chemicals released by the pathogen or lymphocytes

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14
Q

adhesion

A

firm connection between phagocytes membrane and the antigen

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15
Q

ingestion and intracellular digestion

A

pathogen engulfed and surrounded by a membrane e lines vacuole where lysosomes containing enzymes break it down

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16
Q

disposal

A

the parts that cannot be used in metabolism are ejected by exocytosis

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17
Q

specific immune repose - clonal expansion

A

-specific lymphocytes are not produced in response to an infection they already excst
-there are so many different types there is high probability that one of these will have a protein on surface that is complementary to an antigen
-when infection occurs the one type of cell that recognises the antigen will divide to build up the numbers of that particular type

18
Q

apotosis

A

cell death

19
Q

when lymphocytes recognise and rwespsond to cells in our own body

A

-in the foetus lymphocytes rarely come into contact with pathogens so collude exclusively with self cells
-some of the receptors fits those pf the body cells these lymphocytes are then suppressed
-this leaves only lymphocytes that might recognise non-self antigens

20
Q

t lymphocytes

A

mature in thymus gland
-cell mediated immune its ie. immunity requiring the cell to be present
-have receptor proteins that can detect antigens and form antigen receptors complexes
-helped T cells th
cytoxic T cells tc
-antigen recognition site binds to antigens

21
Q

b lymphocytes

A

form and mature in bone marrow

22
Q

activTION of t helper cell

A

1)bacterium with antigen on surface
2)bacterium engulfed by macrophage
3)macrophage presents antigens on major hustocompatability complexes becomes an antigen presenting cell

23
Q

Explain why the secondary immune response is much more rapid than the primary one

A

Because of the production of memory cells the secondary response is much more faster than the primary one . The memory cells differentiate into plasma b cells rapidly to produce much more antibodies at a faster rate against the pathogens .

24
Q

Primary immune response - B cell clonal selection

A

B cells bind to antigens the antigen enters by endocytosis and then is presented on surface of cell it has become an antigen presenting cell

25
Humoral immune response
Plasma cells secrete lapse amount of antibodies Antibodies bind to antigens and stop disease by stickin cells together into large clumps targeting them for destruction by phagocytes Preventing viruses and bacteria from infecting cells Binding to free toxin proteins
26
Antibodies
Composed of four polypeptide chains 2 heavy chains 2light chains Joined by disulphide bonds Form a Y shaped structure The stem =constant region The ends of the arms =variables regions that bind to the antigen
27
Contrast the cell mediated and humoral response to pathogens
Humoral response produces antigen specific antibodies Humoral response also more rapid whereas cell mediated is delayed
28
Monoclonal antibodies
Antibodies produced from a single group of genetically identical B-cells specific to one type of antigen They are all identical in structure
29
Why are monoclonal antibodies same in structure
They have the Same primary structure as they are coded for by the same genes so they have the same secondary and tertiary structures as a results
30
Uses of monoclonal antibodies
1)cancer treatments to target cytotoxic drugs to the cancer cells The monoclonal antibody carries a cytotoxic drug to the cancer cells it is specific to the antigen on the cancer cells the drug is activated to kill the cancer cells 2)cancer treatment to block the growth factors that stimulate cell division 3)medical diagnosis -eg.hiv test ,pregnancy test,Covid lateral flow 4)transplant surgery to knock out T cells targeting the foreign antigen
31
Pregnancy testing
-the placenta in a pregnancy women produces a hormone hcg in mothers urine -monoclonal antibodies immobilised in coloured beads on a test strip -when urine is applied hcg will bind to antibodies to form complex -hcg antibody colour complex along the strip until trapped by a different type of antibody Completed accumulate t produces a coloured trace
32
ELISA test
-detects the presence of specific antibodies or antigens in the blood Uses antibodies with an enzyme attached -an Elisa test may be used to diagnose diseases such as HIV,Lyme diseases ,syphilis -the test is extremely sensitive and therefore can detect a small quantity of molecule
33
Ethical issues
-use of mice -informed consent -dangers in trialling the drug
34
Pronlem of using mice
Mice used to produce antibodies and tumour cells so deliberately induce cancer in the mice there are guidelines drawn up to minimise suffering
35
Deaths using monoclonal antibodies
When treating multiple sclerosis’s It is important that patients have full knowledge of the risks and benefits of these drugs before giving permission for them to be used
36
Testing the safety of new drugs
200( healthy volunteers trial of new antibody caused multiple organ failure all volunteers survived but it raises issues about the conduct of drug trials
37
Two forms of immunity
Active and Passive
38
Herd immunity
If enough people are immune to a pathogen then the remaining people are often protected due to a lack of hosts for the pathogen to reproduce in
39
40
Antibiotics
Prevent growth of bacteria Two types -bacteriocidal + bacteriostatic
41
Why antibiotics have no effect on eukaryotic cells
They don’t have a cell wall and their ribosomes are a different size which means antibiotics can’t bind to them
42
Why antibiotics have no effect on viruses
They do not possess either cell wall or ribosomes Replicate inside host cells