Topic 2.3 - Cells and The Imune System Flashcards

1
Q

Define antigen

A
  • Molecules (usually proteins) that can generate an immune response when detected by the body
  • Unique to each cell
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2
Q

Define foreign antigen

A

Antigens that are not normally found in the body

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3
Q

What three ways does the immune system identify foreign antigens?

A
  • Pathogens
  • Abnormal body cells (e.g. cancerous cells)
  • Cells from other organisms from the same species
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4
Q

What three places are antigens presented?

A
  • Surface of cells
  • Surface of host cells
  • Surface of macrophage / phagocyte that has engulfed the pathogen
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5
Q

Define antigen presenting cell

A

An immune cell (macrophage) that processes and presents antigen on its surface to activate other immune cells

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6
Q

Define antigen variation

A
  • Change of surface antigens of pathogens
  • Different antigens formed due to changes in the DNA / RNA of pathogen (mutation)
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7
Q

What are the two types of primary defences?
Give examples

A
  • Physical barriers > skin
    > mucus
    > reflexes (e.g. sneezing, blinking)
  • Chemical barriers > sebum (fatty acids on skin)
    > tears (contains lysosomes)
    > acids in stomach
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8
Q

What are the three types of secondary defences?

A
  • Inflammatory response
  • Haemostasis (blood clotting)
  • Phagocytosis
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9
Q

What happens during inflammatory response?

A
  • Chemicals are released from the granules of leukocytes
  • Made primarily at sites of tissue damage or infection
  • Removes damaged tissue components or pathogens, so that body can begin to heal
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10
Q

What happens during haemostasis?

A
  • Seals damaged blood vessels, preventing significant bleeding
  • Done by platelets
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11
Q

What happens during phagocytosis?

A
  • Phagocyte recognises foreign antigens of pathogen
  • Phagocyte engulfs pathogen
  • Phagocytic vesicle forms around the pathogen
  • Lysosomes, containing lysozymes (digestive enzymes) fuses with phagocytic vesicle to create a phagolysosome
  • Lysozymes hydrolyse / digest the pathogen
  • Pathogen’s antigens are presented on the surface of macrophage
    Becomes an antigen presenting cell
  • Digested pathogen is released out of the phagocytes by exocytosis
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12
Q

Define cellular immune response

A

The immune response that involves the activation of phagocytes and T-cells

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13
Q

Define humeral immune response

A

The immune response that involves B-cells, clonal selection and production of antibodies

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14
Q

Describe the process of cellular immune response

A

1) Phagocytosis > macrophage becomes an antigen presenting cell
2) T-cells > Receptor proteins on its surface that bind to complementary antigens presented on the macrophage
> Corrected T-cells are selected and activated
> Th-cells: release chemical signals that activate phagocytes and B-cells which produce antibodies
> Tc-cells: release molecules to kill pathogens, abnormal, infected or foreign cells

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15
Q

Describe the process of humeral immune response

A

1) B-cells > covered with antibodies
> have complementary antibodies to certain antigens
2) Clonal selection > antibodies on surface of B-cells bind to complementary antigen
3) Clonal expansion > activated B-cells divide by mitosis into plasma cells (clones of B-cells)
4) Antibody production > Plasma cells secrete lots of specific antibodies (monoclonal antibodies)
> antibodies bind to complementary antigen on the pathogen surface to form antigen-antibody complex
> some B-cells differentiate into memory cells
5) Antibodies have two binding sites. This means they can bind to two pathogens at the same time
6) Agglutination > clumping together of pathogens
> Easily engulfed by phagocytes
7) Phagocytes bind to the antibodies and phagocytose many pathogens. It’s leads to destruction of pathogens with the same antigen

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16
Q

Where are T-cells and B-cells developed?

A

Bone marrow

17
Q

How fast is the primary response?
Give reasons

A
  • Slow
  • Not many B-cells that can make the antibody needed
  • Eventually, body will produce enough
  • Body will show symptoms of disease
  • B-cells produces memory cells
  • Person is not immune
18
Q

How fast is the secondary response?
Give reasons

A
  • Faster
  • Antibodies are produced quicker in a higher concentration
  • Clonal selection happens faster
  • Memory B-cells are activated and divide into plasma cells > produce the correct antibody
  • Memory T-cells are activated and divide into correct T-cells > kills cell carrying antigen
  • No symptoms as the antigen is gone before symptoms arise
19
Q

Define immune

A

Ability to respond quickly to the same antigen

20
Q

Define cell signalling

A

Communication between cells

21
Q

What three things does cell signalling involve?

A
  • Antigens
  • Cell surface receptors
  • Cytokines (chemical)
22
Q

Define antibodies

A

Globular proteins secreted by B-cells in response to the presence of foreign antigens

23
Q

What is the structure of an antibody?

A
  • Y-shaped
  • 4 polypeptide chains held together with a disulphide bridge > quaternary structure
23
Q

What are the four regions of an antibody?

A
  • Constant region = same in all antibodies
  • Variable region = specific to the antibody
    = complementary to antigen (has a specific amino acid sequence > primary structure)
  • Binding site > Tertiary structure
  • Hinge region > Allows flexibility and attraction to more than one antigen
24
Define neutralisation
Formation of an antigen-antibody complex, preventing the pathogen from binding to the host cell
25
What are the four protein structures? What bonding do they include? Give a description for each
- Primary > Sequence of amino acids in a polypeptide chains > Peptide bonds - Secondary > Polypeptide chain coils into alpha helix or fold into a beta pleated sheet > Hydrogen bonds - Tertiary > Alpha helix or beta pleated sheet coils further > 3D shape > Hydrogen bonds, ionic bonds and disulphide bridges - Quaternary > Multiple polypeptide chains
26
Where do phagocytes bind to on an antibody?
Constant region
27
Define monoclonal antibodies
Antibody produced from a single clone of genetically identical B-cells
28
Why are antibodies specific?
- Binding site has a specific tertiary structure which is complementary to one antigen - Able to target a specific chemical or specific cell on the body
29
How are monoclonal antibodies produced in the lab?
1) Inject a mouse with specific antigen to stimulate mouse B-lymphocytes to make a particular antibody 2) B-lymphocytes are removed / isolated from the mouse 3) B-lymphocytes are combined with a fast dividing tumour cell 4) Makes a hybridoma cell 5) The hybridoma cell can divide rapidly (mitosis) to produce lots of clones. They all produce the same antibody 6) Cloned cells make the antibody 7) Large amounts of antibody can be collected and purified
30
What are the two uses of monoclonal antibodies?
- Medical diagnosis > monoclonal antibodies bind to target antigen (colour change for positive result) > e.g. pregnancy test, ELISA test - Medical treatment > targeting medication to specific cell types by attaching a therapeutic drug to an antibody > therapeutic drugs are: radioactive substance, toxic drug, chemical which stops cells growing and dividing > e.g. magic bullets, herceptin (breast cancer)