Question 1
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T-Cells are involved in Cellular Response.
Question 2
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Select the correct definitions of a Primary Immune Response.
Question 3
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Why is it beneficial to our immune system that many pathogens have several different antigens?
Answer
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More antigens mean its a bigger pathogen so it'll be noticed more easily
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More antigens mean that more B-Cells and T-Cells can be activated
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It's not beneficial - it's too confusing for the B-Cells and T-Cells
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Antigens stop the toxins being released
Question 4
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[blank_start]Active[blank_end] Immunity is when your own immune system manufactures its own antibodies to tackle the antigen.
[blank_start]Passive[blank_end] Immunity is when you receive antibodies made by another organism.
Question 5
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Active Immunity is long term and offers immediate protection.
Question 6
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[blank_start]Natural Passive Immunity[blank_end] is when antibodies are passed from the mother to the baby through the placenta and/or breast milk.
[blank_start]Natural Active Immunity[blank_end] is when antibodies are produced when you have caught the disease.
[blank_start]Artificial Passive Immunity[blank_end] is when antibodies are injected into you from another organism.
[blank_start]Artificial Active Immunity[blank_end] is when antibodies are produced after exposure to the antigen through a vaccine.
Answer
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Natural Passive Immunity
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Natural Active Immunity
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Artificial Passive Immunity
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Artificial Active Immunity
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Natural Active Immunity
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Natural Passive Immunity
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Artificial Passive Immunity
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Artificial Active Immunity
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Artificial Passive Immunity
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Natural Passive Immunity
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Natural Active Immunity
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Artificial Active Immunity
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Artificial Active Immunity
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Natural Passive Immunity
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Natural Active Immunity
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Artificial Passive Immunity
Question 7
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Antigenic Variation:
Answer
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When pathogens change the antigens on their surface
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Done by mutation
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Doesn't stop the Secondary Immune Response
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Enables vaccines to be made
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Is common among viruses
Question 8
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HIV is known as a [blank_start]retro[blank_end]virus because it stores its genetic information in the form of [blank_start]R[blank_end]NA.
Question 9
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Label this diagram of a HIV.
Answer
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RNA
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Enzyme
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Capsid
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Phospholipid Membrane
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Glycoprotein Receptor
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Core
Question 10
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[blank_start]Indirect[blank_end] ELISAs test for the presence of a specific antibody.
[blank_start]Direct[blank_end] ELISAs test for the presence of a specific antigen.
Question 11
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Label the diagram of an antibody:
Answer
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Antigen Binding Site
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Disulfide Bridge
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Heavy Chain
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Constant Region
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Variable Region
Question 12
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Label this graph:
Question 13
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A phagocyte follows the trail of [blank_start]chemoattractants[blank_end] left by the pathogen up the concentration gradient.
When it gets near the pathogen, the phagocyte starts stretching out its cell membrane around the pathogen. These 'arms' are known as [blank_start]pseudopodia[blank_end] and allow the phagocyte to [blank_start]engulf[blank_end] the pathogen and form a [blank_start]phagosome[blank_end] or phagocytotic vacuole.
[blank_start]Lysosomes[blank_end] in the phagocyte travel to this vesicle, fuse with it (a [blank_start]phagolysosome[blank_end]) and release their [blank_start]lytic[blank_end] enzymes into it, breaking down and destroying the pathogen.
The waste is released in [blank_start]exocytosis[blank_end] and often the antigen(s) of the pathogen are displayed on the cell surface of the phagocyte.
Answer
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chemoattractants
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pseudopodia
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phagosome
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engulf
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Lysosomes
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phagolysosome
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lytic
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exocytosis
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phagocyte
Question 14
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Endocytosis is when something is taken into a cell.
Question 15
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Put these stages of an Immune Response in order of when they occur and match the correct definition to them:
[blank_start]PHAGOCYTES ENGULF PATHOGENS[blank_end] - Phagocyte ingests pathogen and displays its antigens on its cell surface membrane.
[blank_start]T-CELLS ACTIVATED[blank_end] - A [blank_start]T-Cell[blank_end] with a [blank_start]complementary receptor[blank_end] to the antigen comes into contact with the phagocyte.
[blank_start]CLONAL SELECTION[blank_end] - The T-Cell begins [blank_start]rapid mitosis[blank_end], producing [blank_start]daughter cells[blank_end] with the complementary receptors.
[blank_start]IMMUNE RESPONSE[blank_end] - [blank_start]Cytokines[blank_end] are released by the T-Cells, stimulating [blank_start]B-Cells[blank_end] to divide to form [blank_start]plasma and memory cells[blank_end] and phagocytes to perform [blank_start]phagocytosis[blank_end]. [blank_start]Cytotoxic and Memory T-Cells[blank_end] are also created.