4.1.6(Specific immune responses)

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17 Terms

1
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State the name of the process of activating B and T lymphocytes

  • Clonal selection

2
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What are B memory cells

  • Cells that remain in the blood for a long time, providing long-term immunity

3
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What is meant by clonal expansion

  • An increase in the number of cells by mitotic cell division

4
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What is meant by interleukins

  • Interleukins are signalling molecules that are used to communicate between different white blood cells to activate an immune response

5
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What are plasma cells

  • Derived from B lymphocytes, these are cells that manufacture antibodies

6
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State the 4 types of T lymphocytes

  • T helper cells(Th)

  • T Killer cells(Tk)

  • T memory cells(Tm)

  • T regulatory cells(Tr)

7
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Describe where T and B lymphocytes are made and where they mature

  • T lymphocytes are made in bone marrow but mature in the thymus

  • B lymphocytes are made in bone marrow and mature in the bone marrow aswell

8
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Describe the process of activating T helper cells

  • Pathogens are phagocytosed by macrophages and display the invading antigen on the outside of the cell to become a antigen presenting cell(APC)

  • APCs travel to the nearest lymph node to present information about the captured pathogen to the many T helper cells

  • When a T helper cell recognises an antigen on the APC, as it has a complementary receptor, it binds to it and becomes activated

9
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Describe what happens after T helper cells are activated

  • These T helper cells release interleukins:

    • These stimulate the activation of B lymphocytes and T killer cells

    • They also stimulate Phagocytosis by phagocytes

  • Once the correct T helper cell is selected(clonal selection) and activated, they start replicating by mitosis on a large scale - Clonal expansion

10
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Describe how T killer cells are activated

  • They are activated when receptors on their surface detect foreign antigens on the surface of the pathogen

  • They are further stimulated by the release of interleukins

11
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Describe what happens after T killer cells are activated

  • They under go clonal selection and clonal expansion by mitosis

  • They then attack and kill infected cells and cancer cells

12
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Describe the role of T regulatory cells

  • They shut down the immune response after the pathogen has been successfully killed and removed from the body

  • They prevent the body’s lymphocytes from attacking the body’s own cells

  • They supress the immune response of other which blood cells

13
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Describe the process of activating B lymphocytes

  • Antibodies on the B lymphocytes are complementary to the antigens on the pathogen cells. The B lymphocytes bind to the pathogens

  • They then internalise the pathogens and process them and present receptors on the surface of the B cells to become antigen presenting cells(APCs)
    The presented antigen is then recognised by T helper cells specific to the receptor

  • This causes The T helper cells to produce interleukins which causes the activation of B lymphocytes is clonal selection

  • The B lymphocytes then undergo clonal expansion by mitosis

14
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Describe what happens to B lymphocytes after clonal expansion

  • They divide by mitosis during clonal expansion to product genetic clones of its self

  • During this process, 2 new types of cells are created:

    • Plasma cells

    • B memory cells

15
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Describe the role of plasma cells

  • They manufacture and produce and secret loads of antibodies specific to the antigen, so these antibodies attach to antigens on the pathogen and destroy them

16
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Describe the role B and T memory cells

  • After being exposed to the antigen, B and T memory cells are produced

  • These memory cells remain in the body for a long time to provide immunity

17
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Describe how T memory cells and B memory cells are different

  • T memory cells: Receptors recognise specific antigens and respond quickly

  • B memory cells: Lots of memory cells have specific anti bodies on their surface with complementary shape to the antigen, Response of B memory cells is quicker than T memory cells