immunity Flashcards

(37 cards)

1
Q

in order for a microprganism to be considered a pathogen it must

A

gain entry to a host
colonise the tissues of the host
resist the defences of the host
cause damage to the host tissues

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

4 types of pathogen

A

virus
bacteria
protoctists- maleria etc.
fungi

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

how do pathogens cause illness

A

toxins- harmful substances produced by the pathogen that poisons tissues and enzymes
reproduction- rise in number of pathogens can damage a cell sometimes causing it ti burst or hijack resources the cell needs to survive
immune response- result of increased blood flow

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

2 types of toxins

A

exotoxins are secreted by a living normal pathogen whereas endotoxins are released when the pathogen is damaged

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

lymphocytes

A

a type of white blood cell involved in the specific immune response

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

phagocyte

A

a type of white blood cell that engulfs and digests pathogens

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

pathogenicity

A

the ability of a microorganism to cause disease

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

toxins

A

a harmful sunstance produced by a pathogen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

nonspecific immune response

A

the bodys immediate general defense mechanism against pathogens not soecific to any particular pathogen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

non specific defence mechanisms

A

physical barriers
phagocytosis- phagocytes

response in unchanged by exposure to pathogen

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

specific defence mechanisms

A

cell mediated immunity- t lymphocytes
antibody-mediated immunity- b lymphocytes

leads to immunity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

phagocytosis

A

Pathogen produces chemical products which attract phagocyte to the pathogen (chemotaxis)
Phagocytes attach themselves to surface of pathogen
Phagocytes engulf pathogen via a vesicle (called a phagosome)
Lysosomes fuse with the phagosome to form a phagolysosome.
Lysozymes and protease enzymes digest the pathogen by hydrolysing large molecules
Soluble products of digestion absorbed into phagocyte cytoplasm or released by exocytosis.
Some of the pathogens antigens remain in the phagocyte’s cell membrane for antigen-presentation.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

T lymohcytes

A

respond to foreign material inside body cells
made by stem cells in bone marrow but mature in thymus gland
found mainly in lymphatic system

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

cell mediated response

A

t cell responces are described as a cell mediated response because only t cells respond to antigens which are present on cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

antigen presenting cells

A

• T-Cells ‘know’ cells have been invaded because the cells
‘present’ foreign antigen to them (kind of like a flag)
- Phagocytes present some of the pathogen’s antigens on their own cell membranes
- Cells infected by a virus present the viral antigens on their own membrane as a stress signal
- Cancer cells = abnormal proteins (tumour antigens)
- Cells of a transplanted organ will have different shaped antigens on their surface

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

cytotoxic t cells

A

• Cytotoxic T cells destroy abnormal or infected cells.
• They release Perforin which embeds in the cell surface membrane and makes a pore so that any substances can enter or leave the cell.
• This causes cell death.

17
Q

b lymphcytes

A

• Respond to foreign material outside of body cells- in blood/tissue fluid for example (e.g. bacteria)
• Made in bone marrow, mature in bone marrow
•Have antibodies on their surface ‘complementary’ to an invading pathogen’s antigen
• A B-cell only makes 1 type of antibody
When the pathogen attaches to the antibody the B cell divides by mitosis and makes identical clones,

18
Q

the b cell clones become

A
  • Plasma cells- These secrete antibodies directly. They destroy pathogens and toxins. Immediate defense- the primary immune response.
  • Memory Cells- live for decades, circulating in the blood. If encounter the pathogen in later life these develop into plasma cells, and create more memory cells. Quick and intense response-secondary immune response.
19
Q

antigen

A

Substances that are foreign to the organism.
Made of:-
-Protein
- Polysaccharide
- Glycoprotein
Found:-
- Cell surface of microorganism
- Surface of a virus
- On cell surface of a tissue/ organ transplant
- As a free molecule, e.g. toxin

20
Q

antibodies

A

•Also called immunoglobulins
•Found in plasma, tissue fluid, milk
•Made of 4 polypeptide chains (2 FeesiA and 2 light chains)
• Hinge region (disulphide bridge) allows them to change shape to fit
around antigen.
• Each antibody fits a specific antigen.

21
Q

antibody- antigen complex

A

Agglutination of antigens (stick together)
Immobilises microbes/ blocks antigens so cannot attach to host cells
Block active region of toxin so it is harmless
Prepare complex for ingestion by phagocytes

22
Q

polyclonal antibodies

A

PolvcIonal antibodies are naturally produced in an immune response. Different plasma cells secrete antibodies, resulting in a variety of different antibodies against a specific antigen.

23
Q

monoclonal antibodies

A

Monoclonal antibodies (mAbs)
are antibodies produced from clones of a single plasma cell and are therefore all identical.

24
Q

retrieving from mice or rabbits

A

A specific antigen is injected into the animal, stimulating the production of plasma cells.
The plasma cells are removed from the animal and fused with cancerous myeloma cells from normal mice.
These form immortal hybridoma cells, which can produce a single type of antibody indefinitely.

25
problems with monoclonal antibodies
The problem with using mouse-derived (murine) mAbs in humans is that they may be recognized as foreign. This will trigger an immune response, which quickly inactivates the mAbs. The immune response can be minimized by using genetic engineering to create humanized mAbs. These consist of mainly human polypeptide chains, with only the amino acids at the antigen-binding site derived from mice.
26
eliza
This technique is performed to detect the presence and/or amount of a target protein/antigen of interest. Or it can be used to detect if a person contains antibodies for a certain antigen. This process can be used to detect for allergies or infection. An antibody is used which has an enzyme attached to it; this will catalyse the conversion of a substrate to a coloured product. The intensity of the colour can be an indicator of the quantity of antigen/antibody
27
eliza test steps
The antigen for the infection that is being tested for is immobilised to the bottom Wash the well several times to remove any antigen molecules that did not stick Add an antibody which is specific for our antigen We wait to allow the antibody molecules to stick to the antigen molecules Wash the well several times to remove any excess antibody Molecules A second antibody is added. The 2nd antibody specifically binds to the 1st. The second antibody is attached to an enzyme molecule Next, we wash again to removed any unbound antibody Add substrate for the enzyn The enzyme converts the substrate into a product molecule which is coloured The intensity of the colour can be used to determine the amount of antigen. This makes the ELIZA a quantitative test
28
29
3 uses if monoclonal antibodies
pregnancy tests treating cancer HIV ELIZA test
30
ethical issues of monoclonal antibodies
• Creating monoclonal antibodies requires the use of mice to produce antibodies and tumour cells which leads to ethical debates as to whether the use of animals is justified to enable the better treatment of cancers in human and to detect diseases.
31
passive immunity
• Is produced by the introduction of antibodies into individuals from an outside source. • No direct contact with the pathogen or its antigen is necessary to induce immunity.
32
adaptive immunity
• Is produced by stimulating the production of antibodies by the individuals own immune system. • Natural/ artificial immunity.
33
vaccines
Vaccines stimulate the production of antibodies and memory cells against the target pathogen without causing illness.
34
draw the human immunodeficiency virus
envelope protein envelope viral genome nucleocapsid viral tegumant
35
retrovirus
• This means it contains RNA (ribonucleic acid) rather than DNA (deoxyribonucleic acid •Viral DNA is made from viral RNA by reverse transcription using the viral enzyme reverse transcriptase. • Viral DNA is incorporated into host DNA in the nucleus by viral enzyme integrase
36
getting infectid with hiv
1. p120 molecules on the HIV bind to CD4 receptor proteins on T helper lymphocytes and macrophages. 2. The Virus outer envelope fuses with the cell membrane 3. Viral RNA + enzymes from the HIV are injected into the T cell 4. The viral DNA is transcribed and translated by the host cell to produce new viral proteins. (10° new viruses can be produced per day!) 5. Transcribed RNA plus viral proteins are assembled together to form new viruses 6. The new viruses leave the cell by budding, taking some of the host cell membrane to form the viral envelope. This kills the T helper cells
37
loss of t helper cells
• T cells are killed when the HIV virus exits the T cell via budding. • Infected T helper cells are also destroyed by T killer cells. • So the number of T helper lymphocytes decreases over time. • Loss of T helper cells results in the loss of activation of both B and T cells so the effectiveness of the specific immune response to combat infection is subsequently reduced.