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6.1-6.4 IMMUNOLOGY

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6.1-6.4 IMMUNOLOGY
Non-specific mechanisms
- Physical barriers
- Protective covering
- The skin
- Epithelia covered in mucus
- Lungs
- Pathogens stick to mucus
- Transported away by cilia
- Swallowed into stomach
- Transported away by cilia
- Hydrochloric acid in stomach
- low pH
- Most of the enzymes of the pathogen denature
- low pH
- Protective covering
- Phagocytosis
- The phagocyte is attracted to the pathogen by chemoattractants
- It moves towards the pathogen along a concentration gradient
- The phagocyte binds to the pathogen
- They engulf the pathogen to form a phagosome
- Lysosomes move towards the vesicle and fuse with it
- The lysosomes release lytic enzymes into the phagosome
- The enzymes break down the pathogen
- The breakdown products are absorbed by the phagocyte
- The enzymes break down the pathogen
- The lysosomes release lytic enzymes into the phagosome
- Lysosomes move towards the vesicle and fuse with it
- They engulf the pathogen to form a phagosome
- The phagocyte binds to the pathogen
- It moves towards the pathogen along a concentration gradient
- The phagocyte is attracted to the pathogen by chemoattractants
- Do not distinguish between one type of pathogen and another
- They respond to all pathogens in the same way
- They act immediatley
- They respond to all pathogens in the same way
- Physical barriers
Specific mechanisms
- Cell-mediated response
- T cells
- Mature in the Thymus gland
- Respond to foreign material inside body cells
- Respond to own cells altered by viruses or cancer and to transplanted tissues
- Stages in T lymphocyte response
- Pathogens invade body cells or are taken in by phagocytes
- The phagocyte/cancer cell/infected body cell places antigens from the pathogen on its cell-surface membrane
- Receptors on certain T helper cells fit exactly onto these antigens
- This activates other T cells to divide rapidly by mitosis and form a clone
- The clones T cells
- develop into memory cells that enable a rapid response to future infections by the same pathogen
- stimulate phagocytes to engulf pathogens by phagocytosis
- stimulate B cells to divide
- kill infected cells
- The clones T cells
- This activates other T cells to divide rapidly by mitosis and form a clone
- Receptors on certain T helper cells fit exactly onto these antigens
- The phagocyte/cancer cell/infected body cell places antigens from the pathogen on its cell-surface membrane
- Pathogens invade body cells or are taken in by phagocytes
- How T cell kill infected cells
- Produce a protein that makes holes in the cell surface membrane
- The cell becomes freely permeable to all substances and dies as a result
- Produce a protein that makes holes in the cell surface membrane
- T cells
- Humoral response
- B cells
- Mature in the bone marrow
- Produce antibodies
- Respond to foreign material outside body cells
- Respond to bacteria and viruses
- B cell immunity
- The surface antigens of the invading pathogens are taken up by B cells
- The B cells process the antigens and present them on their surfaces
- T helped cells attach to the processed antigens on the B cells thereby activating them
- he B cells are activated and divide by mitosis to give a clone of plasma cells
- The clones plasma cells produce antibodies that exactly fit the antigens on the pathogen's surface
- The antibodies attach to antigens on the pathogen and destroy them - this is a primary immune response
- Some B cells develop into memory cells. They respond to future infections by dividing rapidly and developing into plasma cells.
- This is a secondary immune response.
- Plasma cells
- Short life span
- Primary response
- Short life span
- Memory cells
- Long life span
- Secondary response
- Long life span
- B cells
- Distinguish between different pathogens
- Less rapid
- Provide long lasting immunity
- Involve lymphocytes
- Cell-mediated response
How lymphocytes recognise their own cells
- There are around 10 million different lymphocytes each capable of recognising a different chemical shape
- In the fetus, these lymphocytes are constantly colliding with other cells
- Infection in the fetus is rare because it is protected from the outside world by the mother and placenta
- Lymphocytes collide almost exclusively with self material
- Some lymphocytes will have receptors that exactly fit the body's cells
- These lymphocytes die or are supressed
- The only remaining lymphocytes fit non-self material
- These lymphocytes die or are supressed
- Some lymphocytes will have receptors that exactly fit the body's cells
- Lymphocytes collide almost exclusively with self material
- Infection in the fetus is rare because it is protected from the outside world by the mother and placenta
- In the fetus, these lymphocytes are constantly colliding with other cells
- There are around 10 million different lymphocytes each capable of recognising a different chemical shape
Antigens
- Any part of an organism that is recognised as non-self
- Stimulates an immune response
- Usually proteins
- Part of cell-surface membranes or walls
- Micro-organisms
- Diseased cells
- Part of cell-surface membranes or walls
- Any part of an organism that is recognised as non-self
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- AQA BIOLOGY Mind Map on 6.1-6.4 IMMUNOLOGY, created by Heather Mansfield on 17/04/2014.
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- Heather Mansfield
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