Cell Recognition and the Immune System Flashcards

1
Q

Define antigen (PST)

A
  • A protein/glycoprotein
  • Found on the surface of a cell/pathogen/toxin
  • That triggers an immune response
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2
Q

Define pathogen

A

A microorganism that causes disease

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3
Q

What do antigens allow the immune system to identify? (TPCC)

A
  • Toxins
  • Pathogens and pathogen-infected cells
  • Cancer cells (have abnormal antigens in their cell surface)
  • Cells from other individuals of the same species (will have foreign antigens unless from generically identical donor)
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4
Q

Role of the innate immune system

A

Destroys anything that is recognised as foreign - it is non-specific and fast

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5
Q

Role of the adaptive immune system

A

Targets a specific antigen - it is specific, slower and provides long-term immunity

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6
Q

What is the order of resort for the innate immune system? (BTIFP)

A
  • Barriers
  • Thrombocytes
  • Inflammation
  • Fever
  • Phagocytosis
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7
Q

Give examples of barriers and what do they do?

A
  • Skin
  • HCl in stomach
  • Cilia/mucus in trachea
  • They prevent the entry of every microbe
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8
Q

What do thrombocytes do?

A

Clotting if the barrier (specifically the skin) is broken

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9
Q

Why does inflammation happen?

A
  • If clotting doesn’t stop pathogens from entering
  • Increases the concentration of leukocytes in the blood plasma in that area to fight the pathogen
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10
Q

Why does fever happen?

A

High temperature
To denature the enzymes in the pathogen so it can’t reproduce

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11
Q

What happens if barriers, thrombocytes, inflammation and fever don’t work?

A

Phagocytosis

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12
Q

What are the different types of phagocytes? There are 6.

A
  • Eosinophil
  • Basophil
  • Neutrophil
  • Monocyte
  • Macrophage
  • Dendritic cell
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13
Q

Outline the process of phagocytosis (12)

A

1) Chemical attraction between pathogen and phagocyte occurs (due to chemical secretions of the phagocyte). This is known as chemotaxis
2) Phagocyte moves towards the pathogen down a concentration gradient
3) Receptors on the CSM of the phagocyte bind to chemicals on the CSM of the pathogen
4) Phagocyte engulfs the pathogen, surrounding it using pseudopodia
5) Pathogen gets trapped in a vesicle - a phagosome is formed
6) A lysosome is synthesised by the phagocyte
7) Lysosome fuses with the phagosome, forming a phagolysosome
8) Hydrolytic enzymes (lysozymes) from the lysosome hydrolyse the pathogen
9) The hydrolysed pathogen debris is released by exocytosis
10) If the pathogen is a monocyte/macrophage, the phagocyte presents the pathogen’s antigens on its cell surface membrane and so becomes an APC. However phagocyte will still keep its own antigens (MHCs) on its CSM so that it isn’t identified as foreign
11) T helper cells come near the phagocyte and identify the foreign antigen
12) The adaptive immune response is triggered

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14
Q

Summarise Phagocytosis in key words

A

Chemotaxis, attach, pseudopodia, engulf, phagosome, lysosome, phagolysosome, hydrolytic enzymes, exocytosis, APC, adaptive immune response

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15
Q

Where do T-lymphocytes differentiate?

A

Thymus gland

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16
Q

What does the cell-mediated response target? (AVCT)

A

Cells which have a foreign antigen presented on their CSM. These are:
- APCs
- Virally infected cells
- Cancer cells
- Transplanted cells

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17
Q

What is the cell-mediated response less effective at targeting? (EF)

A
  • Extracellular pathogens eg bacterial cells
  • Free antigens eg allergens, toxins
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18
Q

How does the cell-mediated response start?

A
  • An adaptable CD4 receptor from a T helper cell fits exactly onto a foreign antigen presented by an APC
  • This causes the T Helper cell to rapidly divide by mitosis and form many genetically identical clones of itself (T-memory cells)
19
Q

After the T-helper cell divides by mitosis to form T-memory cells, what 4 things happen?

A

1) T-memory cells circulate in the blood and readily respond to any future infection by the same pathogen
2) Cytotoxic T-cells are activated and release perforins - a protein which makes holes in the CSM of abnormal cells, causing it to become permeable —> lysis —> cell dies as CSM can’t function.
The T-helper cell also releases cytokines. These do 2 things:
3) Send messages to phagocytes to get more of them to destroy the pathogen
4) Stimulates B-lymphocytes to divide so complementary antibodies can be produced - this starts the humoral response

20
Q

What is the most common cytokine?

A

Interlukin

21
Q

Why are B-lymphocytes called so?

A

Because they differentiate in the bone marrow

22
Q

Where does the humoral response take place?

A
  • In the body’s humour - the blood and lymph
23
Q

Where does the cell-mediated response take place?

A

Within infected cells

24
Q

What does the humoral response produce?

A
  • Complemetary antibodies
25
What is the purpose of the humoral response?
To prevent cell damage proactively
26
What does the humoral response target? (BAT)
- Bacterial cells - Allergens - Toxins
27
What happens when a T-helper cell releases cytokines?
- Sends messages to phagocytes to get more of them to destroy the pathogen - It stimulates B-cells to divide
28
How exactly are B-cells stimulated by cytokines?
- Cytokines stimulate the B-cell to synthesise the foreign antigen - B-cell then presents this foreign antigen on its surface (MHC)
29
Another T-helper cell will then come and recognise this antigen on the B-cell’s CSM. What 2 things can happen next? (PC)
1) The B-cell will become a B-plasma cell: - Produces antibodies and releases them free into the blood stream - These antibodies are complementary to a particular antigen - Next time the pathogen is encountered, antibodies bind to the antigen —> antigen-antibody complex 2) The B-cell will undergo clonal selection: - It divides by mitosis to produce B-memory cells —> genetically identical clones that are specific to one antigen - Next time pathogen is encountered, these can differentiate into B-plasma cells and secrete antibodies
30
Where are antibodies stored?
In the spleen
31
What are immunoglobulins?
Globular proteins of the immune system
32
Which type of cell produces antibodies?
B-plasma cells
33
Define antibody
- A Y-shaped protein - Produced by B-plasma cells - That binds specifically to antigens - To agglutinate/opsonise/neutralise pathogens
34
What is the purpose of agglutination?
- Sticks pathogens together - To make them bigger and more recognisable by other cells of the immune system - Also so that more than one pathogen can be destroyed by the phagocyte at once - Therefore it increases speed of the secondary immune response
35
What is the purpose of opsonisation?
- Antibodies coat the pathogen (antigen-antibody complexes) - Therefore the pathogen is labelled - So it is highlighted to the rest of the immune system to be destroyed
36
What 3 things do antibodies do?
Agglutination, Opsonisation, Neutralisation of toxins released by the pathogen
37
Describe the structure of an IgG antibody.
- 2 heavy chains, 2 light chains - Heavy chains have more amino acids than light chains - All PP chains are joined together by disulphide bridges - Have a constant region - ~95% of the mass of the antibody and is the same across all antibodies of the same type - Have 2 identical variable regions. These are the binding sites - specific amino acid sequence unique to a particular antigen. Matches the epitope of an antigen
38
Why do IgG antibodies have Disulfide bridges?
They are very strong and resist pressure changes
39
What does the constant region determine?
The mechanism used to destroy the antigen
40
What does the hinge region in the middle (not present in all antibodies) enable?
- Gives flexibility to the antibody - Allowing the binding sites to be at different angles when binding to antigens
41
What is the epitope of an antigen?
- The part of the antigen which binds to the antibody
42
Maximum number of antigens an IgG antibody can bind to at a a given point in time
2
43