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Lesson Objectives.
1. Understand how pathogens cause disease. 2. Recall phagocytosis and the role of lysosomes in phagocytosis. 3. Know what an antigen is. 4. Know that there are two types of lymphocytes. 5. Know the role of T cells in cell mediated immunity. 6. Know the role of B cells in humoral immunity.
1_3_necrosis.mov
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Immune response
Invading pathogens stimulate an immune response phagocytes are the first line of response but the long term response is governed by antibodies. An immune response is a response to the presence of an antigen its purpose is to remove the antigen. Cells and molecules that are part of the body are described as self since the immune system has become desensitised to them. Antigens are therefore described as non self particles.
1_3_necrosis.mov
This picture shows HIV budding and bursting out of an infected cell. Viruses are not considered to be living organisms by many biologists because they are unable to reproduce on their own.
To reproduce they must invade a host cell and use the hosts cellular mechanisms to produce new virus copies.
This budding HIV has been made by the infected cell.
hiv_life_cycle-
Eosinophil - In the cell's cytoplasm (yellow) are many lysomomes (purple), used to destroy invading organisms. They are capable of ingesting and destroying foreign particles by a process known as phagocytosis.
1_7_phagocytosis.mov 1_11_macrophage.mov
Macrophage
Nucleus
Macrophage
Antigens from the 2 dismantled invader are attached to MHC self proteins
Macrophage
MHC proteins and 3 their attached antigens are displayed on macrophage surface
Macrophage
MHC proteins and 3 their attached antigens are displayed on macrophage surface
Macrophage
Macrophage
Helper T cells recognize 4 antigens and MHC proteins and bind to the macrophage, initiating a series of immune events
Antigens from the 2 dismantled invader are attached to MHC self proteins
Macrophage
Nucleus Helper T cells recognize 4 antigens and MHC proteins and bind to the macrophage, initiating a series of immune events
Cell Mediated immunity. T-lymphocytes are involved in the cell mediated response. They have receptors on their surfaces which bind to antigens directly. Killer T-cells then destroy the foreign cell. The HIV virus destroys killer T-cells. T-lymphocytes are associated with immune responses in tissues rather than in the blood.
Virus
Virus
Macrophage
Virus
Macrophage
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Interleukin-1
Macrophage
Virus
Interleukin-1
Helper T cell T cell receptor that fits the particular antigen Interleukin-2
Macrophage
Virus
Interleukin-1
Helper T cell T cell receptor that fits the particular antigen Interleukin-2
Macrophage
MHC protein
Antigen-presenting cell
Virus
Interleukin-1
Helper T cell T cell receptor that fits the particular antigen Interleukin-2
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Cytotoxic T cell
Virus
Interleukin-1
Helper T cell T cell receptor that fits the particular antigen Interleukin-2
Macrophage
Cytotoxic T cell
Virus
Interleukin-1
Helper T cell T cell receptor that fits the particular antigen Interleukin-2
Macrophage
Cytotoxic T cell
Virus
Interleukin-1
Helper T cell T cell receptor that fits the particular antigen Interleukin-2
Macrophage
Cytotoxic T cell
Virus
Interleukin-1
Helper T cell T cell receptor that fits the particular antigen Interleukin-2
Macrophage
Cytotoxic T cell
Virus
Interleukin-1
Helper T cell T cell receptor that fits the particular antigen Interleukin-2
Macrophage
MHC protein Viral antigen Antigen-presenting cell Proliferation Infected cell destroyed by cytotoxic T cell
Cytotoxic T cell
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Processed antigen
B cell
Antigen
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Helper T cell
Antigen Macrophage
Processed antigen
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Helper T cell
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Processed antigen
Helper T cell
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Interleukin-1
Helper T cell
Antigen Macrophage
Processed antigen
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Interleukin-1
Helper T cell
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Processed antigen
B cell
Interleukin-1
Helper T cell
Antigen Macrophage
Processed antigen
B cell
Interleukin-1
Helper T cell
Antigen Macrophage
Memory cell
Processed antigen
B cell
Bacteria
Viruses
Bacteria
Viruses
Innate response
Bacteria
Viruses Cytokines
Cilia
Innate response
Antimicrobial secretions
Bacteria
Viruses
Innate response
Bacteria
Viruses
Innate response
Physical Cilia Cytokines barriers Antimicrobial secretions Mucous membranes Macrophages Macrophages present antigens
Acquired response
Cellular response
Humoral response
T cells
B cells
Bacteria
Viruses
Innate response
Physical Cilia Cytokines barriers Antimicrobial secretions Mucous membranes Macrophages Macrophages present antigens
Acquired response
Cellular response
Humoral response
T cells
B cells
Cytotoxic T cells
Bacteria
Viruses
Innate response
Physical Cilia Cytokines barriers Antimicrobial secretions Mucous membranes Macrophages Macrophages present antigens
Acquired response
Cellular response
Humoral response
T cells Cytokines
B cells
Cytotoxic T cells
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Viruses
Innate response
Physical Cilia Cytokines barriers Antimicrobial secretions Mucous membranes Macrophages Macrophages present antigens
Acquired response
Cellular response
Humoral response
T cells Cytokines
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Memory B cells
Cytotoxic T cells
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Physical Cilia Cytokines barriers Antimicrobial secretions Mucous membranes Macrophages Macrophages present antigens
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T cells Cytokines
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Memory B cells
Cytotoxic T cells
Plasma cells
Bacteria
Viruses
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Physical Cilia Cytokines barriers Antimicrobial secretions Mucous membranes Macrophages Macrophages present antigens
Acquired response
Cellular response
Humoral response
T cells Cytokines
B cells
Memory B cells
Cytotoxic T cells
Plasma cells
Antibodies
Bacteria
Viruses
Innate response
Physical Cilia Cytokines barriers Antimicrobial secretions Mucous membranes Macrophages Macrophages present antigens
Acquired response
Cellular response
Humoral response
T cells Cytokines
B cells
Memory B cells
Cytotoxic T cells
Plasma cells
Antibodies
clonal_selection.mov
Immunoglobulin G antibody molecules, coloured transmission electron micrograph (TEM). IgG is the most abundant human immunoglobulin, and is found in all body fluids. Each Yshaped molecule bears two arms that can bind to specific antigens, for instance bacterial or viral proteins. In doing this they mark the antigen for destruction by phagocytes, white blood cells that ingest and destroy foreign bodies. They can also kill some pathogens directly, and can neutralise toxins.
..\cells alive\ECB\media\molecular_models\04.8-antibodies.mov
Secondary immune response. Not all lymphocytes become plasma cells some become memory cells which stay dormant in the blood. The plasma cells die once the infection is over but the memory cells dont. If a second infection occurs memory cells respond immediately by producing antibodies and dividing producing more plasma cells. This is the secondary immune response. They secrete more antibodies more quickly this is why the secondary immune response is greater and faster.
Primary immune response caused by the secretion of antibodies from plasma B-lymphocytes
Passive immunity is a temporary type of immunity. Babies are naturally passively immune to a number of diseases when they are born because their mothers antibodies cross the placenta into their blood stream. Babies also gain these antibodies whilst being breast fed. They have no memory cells being formed though and after a while antibodies break down so the immunity goes. This passive immunity allows the baby a chance for it to develop its own active immunity.
Passive immunity
Passive immunity is a temporary type of immunity. Babies are naturally passively immune to a number of diseases when they are born because their mothers antibodies cross the placenta into their blood stream. Babies also gain these antibodies whilst being breast fed. They have no memory cells being formed though and after a while antibodies break down so the immunity goes. This passive immunity allows the baby a chance for it to develop its own active immunity.
Vaccines
Whilst your immune system is manufacturing Blymphocytes you suffer from a disease. Vaccination allows us to avoid this by building up Blymphocytes and the antibodies needed to fight a disease without the microbe being present and increasing in numbers at the same time (which is what causes the disease) This means that we can get the immunity without getting the symptoms. Vaccine.swf vaccination.mov
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Artificial immunity Vaccines give you artificial immunity. Its active immunity because your body makes its own antibodies and will produce memory cells. To prevent the disease in the future. Its called artificial immunity because you have not actually caught the disease in the natural way your body has been tricked into reacting to a harmless pathogen.
Instant immunity
After cuts or bites people may be injected with tetanus antibodies rather that the tetanus pathogen. This gives you artificial immunity instantly. It is however passive because your B-lymphocytes have not been involved in the production of the antibodies therefore there will be no memory bells. The immunity will wear off when the antibodies break down.
Herd immunity
Vaccines not only protect the people vaccinated but they reduce the occurrence of the disease those not vaccinated are less likely to catch it. This is called the herd immunity effect. This is one of the factors which helped in the irradiation of the small pox virus following a WHO vaccination program. herd immunity animation.swf
Monoclonal Antibodies
Lesson Objectives 1. 2. 3. 4. 5. Understand how monoclonal antibodies in enabling the targeting of specific substances and cells. Evaluate methodology, evidence and data relating to the use of vaccines and monoclonal antibodies Discuss ethical issues associated with the use of vaccines and monoclonal Antibodies Explain the role of the scientific community in validating new knowledge about vaccines and monoclonal antibodies, thus ensuring integrity Discuss the ways in which society uses scientific knowledge relating to vaccines and monoclonal antibodies to inform decision-making.
Monoclonal Antibodies.swf
http://www.sumanasinc.com/webcontent/animations/content/ELISA.html