3.2.4 Cell recognition and the immune system 2 Flashcards

1
Q

The humoral response

A

-the antibodies involved are soluble in the blood and tissue fluid of the body

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2
Q

The humoral response

Role of B cells/lymphocytes

A

The humoral response
-produced in primary immune response
-B cell / lymphocyte
└has antibodies on its surface
└which are specific and complementary to only one antigen
-clonal selection
└is the selection and activation of the specific B cell
└by macrophages / antigen presenting cells /T helper cells / cytokines
-clonal expansion
└is where the selected cell divides by mitosis to form clones
-B cells differentiate and specialise
-B cells form plasma cells
└which produce antibodies
└which are, specific and complementary to the antigen
-B cells form memory cells
└memory cells are long-lived and remain in body
└they provide a secondary response
└which is a faster and stronger response to subsequent exposure of same antigen

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3
Q

B cells

A
  • type of white blood cell

- covered with antibodies which are specific and complimentary to different antigens

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4
Q

Clonal selection

A

-the selection and activation of the specific B cell

└by macrophages / antigen presenting cells /T helper cells / cytokines

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5
Q

Clonal expansion

A

-where the selected cell divides by mitosis to form clones

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6
Q

Antibody

Definition

A

-large Y-shaped protein produced by B-cells/plasma cells with antigen-specific receptors

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7
Q

Antibody

Role in immune response (to bacterium/viruses)

A

-variable region binds to antigen on the surface of the pathogen
└as the variable region specific and complimentary to the antigen
-they agglutinate pathogens
-then immobilise pathogens
-they combine with pathogen to stop entry to cell
-they break wall of bacterium open (lysis)
-the constant region, attracts phagocytes and makes it easier to engulf bacterium

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8
Q

Antibody specificity

–why the antibody will only detect this antigen

A
  • the antibody has a specific primary structure
  • and the specific shape of the binding site
  • is complimentary to and binds with the antigens (on the pathogen)
  • and forms a complex between antibody and antigen
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9
Q

Antibody
Structure
List

A
Antigen-binding site
Light chain
Heavy chain
Receptor binding site
Variable region (different in different antibodies)
Constant region
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10
Q

Antibody

Structure

A

-four polypeptide chains
└one long pair of chains: heavy chains
└one shorted pair of chains: light chains

-each antibody has a specific binding site which fits precisely onto a specific antigen → antigen-antibody complex
└binding site is different on different antibodies so is called a variable region
└sequence of amino acids at binding site form specific 3d shape → binds directly to specific antigen

-the rest of the antibody is known as the constant region which binds to receptors of cells such as b cells

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11
Q

Antibody

Structure to function

A

-variable region
└= antigen binding site
└the shape of the variable region is specific and complimentary to the antigen= bind to antigen
-hinge region
└allows flexibility
└so it can bind with more than one pathogen
-constant region
└to hold tertiary structure of molecule
└for binding to receptors on cells / phagocytes
-disulphide bonds
└hold polypeptide chains together

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12
Q

How does the antibody lead to the destruction of the antigen?

A

-don’t destroy them directly

└prepare antigen for destruction

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13
Q

What happens when the antigen is a bacterial cell?

A

-antibodies assist destruction in 2 ways:
└cause agglutination of the bacterial cells
└=easier for the phagocytes to locate
└serve as markers
└=stimulate phagocytes to engulf bacterial cells they are attached to

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14
Q

Variable region

Function

A

= antigen binding site

└the shape of the variable region is specific and complimentary to the antigen= bind to antigen

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15
Q

Hinge

Function

A

-allows flexibility

└so it can bind with more than one pathogen

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16
Q

Constant

Function

A

-to hold tertiary structure of molecule

└for binding to receptors on cells / phagocytes

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17
Q

Disulphide bonds

Function

A

-hold polypeptide chains together

18
Q

The formation of an antigen-antibody complex

A

-if antigen is specific and complimentary to the antibody

└forms antigen-antibody complex

19
Q

Agglutination

A

-as antibodies have 2 binding sites, it can attach to two pathogens at the same time
└they can clump together= agglutination
└=easier for phagocyte to engulf

20
Q

Agglutination

Issues

A

-each antibody cam bind to more than one antigen so more than one bacterium
└=agglutination
-an issue as clotting occurs if blood transfusion is not correct

21
Q

Plasma cells

A

-secrete antibodies to destroy antigen
└usually into blood plasma
-cells survive for a few days
└make vast quantities

22
Q

EQ: Suggest three cells where you might expect to find large quantities of plasma cell
Explain why

A

-rough endoplasmic reticulum
└makes and transport the proteins of the antibodies

-golgi apparatus
└to sort, process and compile the proteins

-mitochondria
└to release the energy needed for such massive antibody production

23
Q

Memory cells

A

-responsible for secondary immune response
-live longer than plasma cells (often decades / rest of life)
-circulate blood and tissue fluid
-divide rapidly into plasma cells and more memory cells when they encounter the same antigen
└the plasma cells produce antibodies needed to destroy pathogen
└new memory cells circulate for future infection
-don’t produce antibodies directly

24
Q

Memory cells

Function

A

-long-term immunity against the original infection
-increased quantity of antibodies
└produced at faster rate than primary immune response
-ensures new infection is destroyed before it can develop enough to cause harm/symptoms
└the person is often totally unaware that they have been infected

25
Q

Importance of memory cells

A
  • memory cells remain from previous infection
  • when an individual comes in contact with the antigen again
  • a rapid secondary response is caused and many antibodies are produced
  • which destroy the antigen before it can cause harm/symptoms
26
Q

Primary immune response

A
  • when an antigen first activates the immune response

- slower

27
Q

Secondary immune response

Why faster than primary immune response

A

Primary immune response
-antigen of the pathogen has to be ingested, processed and presented
-helper t cells link with b cells that then clone
some cells develop into plasma cells that produce antibodies
└these processes occur consecutively and therefore take time

Secondary immune response
-memory cells already present
cloning → development into plasma cells → produce antibodies
└fewer processes means quicker response

28
Q

Cell-mediated vs humeral responses to a pathogen

A

Cell-mediated immunity // Humoral immunity

Involves T cells // Involves mostly B cells

No antibodies // Antibodies produced

First stage of immune response // Secondary
stage of immune response after cell-mediated stage

Effective through cells // Effective through body fluids

29
Q

How vaccines protect people against disease

A
  • vaccines that contain antigens are injected
  • from dead/weakened pathogens
  • this means memory cells are made
  • and upon second exposure memory cells recognise pathogens and become active
  • by rapidly producing more antibodies
  • which destroy pathogens
  • when vaccinated there are fewer people to pass on the disease (herd effect)
30
Q

EQ: Why were 3 injections of the vaccine given

A
  • so there are more antigens
  • and more memory cells
  • so more antibodies are produced
31
Q

Why high mutation rate makes it difficult to develop a vaccine

A
  • a high mutation rate leads to antigens changing (antigenic variability)
  • the vaccine contains specific antigen
  • and antibodies are not complementary to changed antigen, so are unable to bind
32
Q

The concept of herd immunity

A

-more people are immune
└fewer people carry the pathogen
-so unvaccinated people are less likely to contact infected people

33
Q

EQ: why vaccinating a large number of people would reduce significantly the spread of HPV through the population

A
  • virus is not carried in vaccinated people

- so non vaccinated people more likely to come into contact with vaccinated people

34
Q

Types of immunity

A
  • active immunity

- passive immunity

35
Q

Active immunity

A

-immune system makes its own antibodies after being stimulated by an antigen

36
Q

Active immunity

Natural

A

Become immune after catching a disease

37
Q

Active immunity

Artificial

A

Become immune after been given a vaccination containing a harmless dose of antigen

38
Q

Describe how an effective vaccine can produce active immunity to a disease

A

-injection of antigen or weakened/ dead pathogen
└ causes immune response
-pathogen is engulfed by phagocytes
└antigens are presented
-selection / production of active T cells
└which divide by mitosis to produce clones
└secretion of cytokines
└activation of B cells
-B cells divide by mitosis to produce clones
└=production of plasma cells
└which produce of antibodies
└and produce of memory cells
-memory cells remain in body
└=secondary response to infection quicker and greater
└=no symptoms when infected

39
Q

Passive immunity

A

-type of immunity you get after being given antibodies made by a different orgamism
└immune system doesn’t make own antibodies

40
Q

Passive immunity

Natural

A

Baby becomes immune due to antibodies it receives from mother in breast milk

41
Q

Passive immunity

Artificial

A

Become immune after beung injected with antibodies from someone else

42
Q

The differences between active and passive immunity

A

Active immunity/passive immunity

  • requires exposure to antigen/ doesn’t require exposure to antigen
  • takes a while for protection to develop/protection is immediate
  • memory cells are produced/memory cells aren’t produced
  • protection is long term (memory cells)/protection is short term (foreign antibodies broken down)