Cell Recognition And Immune System Flashcards

1
Q

What allows the immune system to identify things?

A

Each type of cell has specific molecules on its surface identify these molecules include proteins and enable the immune systems to identify things

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2
Q

What do the protein molecules enable the immune system to identify

A

Pathogens
Cells from other organisms of the same species
Abnormal body cells
Toxins

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3
Q

Describe non-specific defence mechanism

A

Response is immediate and the the same for all path

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4
Q

Describe specific defence mechanism

A

Respond to slower and specific to each pathogen

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5
Q

Examples of specific and non-specific defence mechanisms

A

Non-specific
-Physical barrier, e.g. the skin
-phagocytosis

Specific
-Cell mediated response, T lymphocytes
-humoural response, B lymphocytes

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6
Q

Define antigen

A

Proteins on surface of foreign cell

Toxin or other foreign substance which induces an immune response in the body, especially the production of antibodies

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7
Q

What protein structure are antigens?

A

Quaternary structure as it has four polypeptide chains joined together

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8
Q

How do b cells respond to foreign antigens?

A

There’s a variety of B cells a different shapes of receptor

T helper cells activate the cells and simulate them to divide by mitosis

cells with the right shape of receptors for antigen is stimulated to divide

plasma cells secrete antibody

antibodies cause pathogens to clump together this is them harmless and prepare them for destruction

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9
Q

Describe the steps of phagocytosis

A

The phagocyte is attracted to the pathogens by chemoattractants moves towards a pathogen a longer concentration gradient. The phagocyte bind the pathogen.
Lysosomes within the phagocyte migrate towards the phagosome formed by engulfing the bacterium.
The lysosomes release the lyric enzymes where they break down the bacteria.
The breakdown products of the bacteria are absorbed by the phagocyte

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10
Q

Define endocytosis

A

The movement of large molecules into cells using vesicles eg phagocytosis

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11
Q

Define exocytosis

A

Movement of lodge molecules out of cells using vesicles the phago lysosomes fused with the cell membrane and release the debris from the broken down pathogen

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12
Q

How do you T cells respond to a foreign antigen?

A

A phagocyte has engulfed a pathogen and displays the antigen on its surface

The antigen is displayed to many different T cells in the lymph node

Clonal selection -stimulated t cell divide many times

Helper T cells – these secrete chemicals which simulate phagocyte cells stimulate the cells to produce antibodies and activate killer t cells

Killer T cells - these bind to cells presenting the complementary antigen

T memory cells formed after injection

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13
Q

Describe perforin

A

Causes perforation in the cell member and making the self full permanent

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14
Q

Describe b lymphocytes

A

Matures in bone marrow
Involved in humoral immunity
Produce antibodies
Responds to foreign material outside body cells
Responds to bacteria and viruses

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15
Q

Describe T lymphocytes

A

Matures in thyroid gland
involved in cell mediated immunity responsd to foreign material inside body cells
response to cells altered by viruses or cancer to transplanted tissue

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16
Q

What protein structure are antibodies?

A

Quaternary structure proteins (4 polypeptide chain)

17
Q

What are antibodies secreted by?

A

B lymphocytes eg plasma cells in response to specific antigen

18
Q

What do antibodies bind to ?

A

Bind specifically to antigens forming antigen antibody complexes

19
Q

How do antibodies lead to the destruction of pathogens ?

A

Antibodies bind to antigens on pathogens forming an antigen antibody complex (specific tertiary structure so binding site /variable region binds to complementary antigen )

Attract phagocytes

Phagocytes bind to the antibodies and phagocytose many pathogens at once

20
Q

What is a monoclonal antibody?

A

Antibody produced from genetically identical /cloned B lymphocytes/plasma cells

So have same tertiary structure

21
Q

How can monoclonal antibodies be used in medical treatments?

A

Monoclonal antibody has a specific tertiary structure/binding site /variable region binds

Complementary to receptor /protein/antigen found only on a specific cell type(e.g cancel cell)

Therapeutic drug attached to antibody

Antibody binds to specific cell forming antigen antibody complex delivering drug

Some mAbs are also designed to block antigens/ receptors on cells

(

22
Q

How can mAbs be used in medical diagnosis?
(E.g pregnancy tests)

A

mAb has a specific tertiary structure /binding site/variable region

Complementary to specific reception /protein /antigen associated with diagnosis

Dye /stain/fluorescent marker attached to antibody Antibody binds

Antibody binds to receptor/protein/antigen forming antigen antibody complex

23
Q

Explain the use of antibodies in the ELISA (enzyme-linked immunosorbent
assay) test to detect antigens

A

Attach sample with potential antigens to well
Add complementary monoclonal antibodies with enzymes attached → bind to antigens if present
Wash well → remove unbound antibodies (to prevent false positive)
Add substrate → enzymes create products that cause a colour change (positive result)

24
Q

Explain the use of antibodies in the ELISA (enzyme-linked immunosorbent
assay) test to detect antigens
(Sandwich elisa)

A

Attach specific monoclonal antibodies to well
Add sample with potential antigens, then wash well
Add complementary monoclonal antibodies with enzymes attached → bind to antigens if present
Wash well → remove unbound antibodies (to prevent false positive)
Add substrate → enzymes create products that cause a colour change (positive result)

25
Q

Explain the use of antibodies in the ELISA test to detect antibodies

A

Attach specific antigens to well
Add sample with potential antibodies, wash well
3. Add complementary monoclonal antibodies
with enzymes attached → bind to antibodies if
present
4. Wash well → remove unbound antibodies
5. Add substrate → enzymes create products that
cause a colour change (positive result

26
Q

Suggest the purpose of a control well in the ELISA test

A

● Compare to test to show only enzyme causes colour change
● Compare to test to show all unbound antibodies have been washed away

27
Q

Discuss some general ethical issues associated with the use of vaccines and
monoclonal antibodies

A

● Pre-clinical testing on / use of animals- potential stress / harm / mistreatment
○ But animals not killed & helps produce new drugs to reduce human suffering
● Clinical trials on humans- potential harm / side-effects
● Vaccines - may continue high risk activities and still develop / pass on pathogen
● Use of drug - potentially dangerous side effects

28
Q

Explain the differences between the primary & secondary immune response

A

Primary- first exposure to antigen
○ Antibodies produced slowly & at a lower conc.
○ Takes time for specific B plasma cells to be
stimulated to produce specific antibodies
○ Memory cells produced
● Secondary- second exposure to antigen
○ Antibodies produced faster & at a higher conc.
○ B memory cells rapidly undergo mitosis to
produce many plasma cells which produce
specific antibodies

29
Q

Explain the effect of antigen variability on disease and disease prevention

A

● Antigens on pathogens change shape / tertiary structure due to gene mutations (creating new strains)
● So no longer immune (from vaccine or prior infection)
○ B memory cell receptors cannot bind to / recognise changed antigen on secondary exposure
○ Specific antibodies not complementary / cannot bind to changed antigen

30
Q

Define vaccine

A

Injection of antigens from attenuated (dead or weekend) pathogens simulating formation of memory cells

31
Q

How do you vaccines provide protection to individuals against disease?

A

Specific be lymphocyte with complementary receptor binds to antigen specific T-helper cell binds to antigen-presenting cell and stimulates cell lymphocytes by mitosis to form clones some differentiate into B plasma cells which release antibodies some differentiate into B memory cells on secondary exposure to antigen be memory cells rapidly divided by mitosis to produce B plasma cellsThese release antibodies faster and that’s a higher concentration.

32
Q

Explain how vaccines provide protection for populations against disease

A

Heard immunity – large proportion of population vaccinated reducing spread of pathogen large proportion of population amuse so they don’t become ill from the infection. Thus there’s fewer infected people to pass on the pathogen/unvaccinated people less likely to come in contact with someone with disease.

33
Q

Describe active immunity

A

Initial exposure to antigen e.g. vaccine or primary infection memory cells involved antibody produced and secreted by B plasma cells slow takes longer to develop long-term immunity as antibody can be produced in response to specific antigen again

34
Q

Describe passive immunity

A

No exposure to antigen
No memory cells involved
Antibody introduced from another organism for example, breastmilk/cross placenta from mother
Faster acting
Short term immunity as antibody hydrolysed

35
Q

Describe the replication of HIV in helper T cells

A

HIV attachment proteins attached to receptors and help a tea cell lipid envelope, fuses of cell surface membrane releasing cap into cell capsule coach releasing RNA reverse transcript reverse transcript convert viral RNA to DNA viral DNA inserted into help a T cell DNA viral protein/captured or produced DNA transcribed into HIV mRNA HIV mRNA translated into new HIV proteins virus particles assembled the released themselves

36
Q

Explain all HIV causes the symptoms of acquired immune deficiency syndrome AIDS

A

HIV facts and kills helper T cells (host cell) as it multiplies rapidly so so tea helper cells con stimulates toxic, B cells and Fargo sites
so be plasma cells can’t release as many antibodies for a glaciation and destruction of pathogen
immune system deteriorates more acceptable to opportunistic infection Pathogens reproduce, releasing toxins and damage cells

37
Q

Explain why antibiotics are ineffective against viruses

A

Viruses do not have metabolic processes/ribosomes and viruses do not have bacterial enzymes/Mirin cell wall