THE IMMUNE SYSTEM.

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Presentation transcript:

THE IMMUNE SYSTEM

Blood Cells

Cells of the Immune System White Blood Cells Phagocytes - Neutrophils - Macrophages Lymphocytes

Phagocytes Produced throughout life by the bone marrow. Scavengers – remove dead cells and microorganisms.

Neutrophils 60% of WBCs ‘Patrol tissues’ as they squeeze out of the capillaries. Large numbers are released during infections Short lived – die after digesting bacteria Dead neutrophils make up a large proportion of puss.

Macrophages Larger than neutrophils. Found in the organs, not the blood. Made in bone marrow as monocytes, called macrophages once they reach organs. Long lived Initiate immune responses as they display antigens from the pathogens to the lymphocytes.

Macrophages

Phagocytosis

Phagocytosis If cells are under attack they release histamine. Histamine plus chemicals from pathogens mean neutrophils are attracted to the site of attack. Pathogens are attached to antibodies and neutrophils have antibody receptors. Enodcytosis of neutrophil membrane  phagocytic vacuole. Lysosomes attach to phagocytic vacuole  pathogen digested by proteases

Lymphocytes Produce antibodies B-cells mature in bone marrow then concentrate in lymph nodes and spleen T-cells mature in thymus B and T cells mature then circulate in the blood and lymph Circulation ensures they come into contact with pathogens and each other

B -Lymphocytes Some activated B cells  PLASMA CELLS these produce lots of antibodies, < 1000/sec The antibodies travel to the blood, lymph, lining of gut and lungs. The number of plasma cells goes down after a few weeks Antibodies stay in the blood longer but eventually their numbers go down too.

B -Lymphocytes Some activated B cells  MEMORY CELLS. Memory cells divide rapidly as soon as the antigen is reintroduced. There are many more memory cells than there were clone cells. When the pathogen/infection infects again it is destroyed before any symptoms show.

Antibodies Also known as immunoglobulins Globular glycoproteins The heavy and light chains are polypeptides The chains are held together by disulphide bridges Each antibody has 2 identical antigen binding sites – variable regions. The order of amino acids in the variable region determines the shape of the binding site

How Abs work Some act as labels to identify antigens for phagocytes Some work as antitoxins i.e. they block toxins for e.g. those causing diphtheria and tetanus Some attach to bacterial flagella making them less active and easier for phagocytes to engulf Some cause agglutination (clumping together) of bacteria making them less likely to spread

Different Immunoglobulins

Number of ag binding sites Site of action Functions Type Number of ag binding sites Site of action Functions IgG 2 Blood Tissue fluid CAN CROSS PLACENTA Increase macrophage activity Antitoxins Agglutination IgM 10 IgA 2 or 4 Secretions (saliva, tears, small intestine, vaginal, prostate, nasal, breast milk) Stop bacteria adhering to host cells Prevents bacteria forming colonies on mucous membranes IgE Tissues Activate mast cells  HISTAMINE

T-Lymphocytes Mature T-cells have T cell receptors which have a very similar structure to antibodies and are specific to 1 antigen. They are activated when the receptor comes into contact with the Antigen with another host cell (e.g. on a macrophage membrane or an invaded body cell)

T-Lymphocytes After activation the cell divides to form: T-helper cells – secrete CYTOKINES  help B cells divide  stimulate macrophages Cytotoxic T cells (killer T cells)  Kill body cells displaying antigen Memory T cells  remain in body

Active and Passive Immunity Active immunity Lymphocytes are activated by antigens on the surface of pathogens Natural active immunity - acquired due to infection Artificial active immunity – vaccination Takes time for enough B and T cells to be produced to mount an effective response.

Active and Passive Immunity B and T cells are not activated and plasma cells have not produced antibodies. The antigen doesn’t have to be encountered for the body to make the antibodies. Antibodies appear immediately in blood but protection is only temporary.

Active and Passive Immunity Artificial passive immunity Used when a very rapid immune response is needed e.g. after infection with tetanus. Human antibodies are injected. In the case of tetanus these are antitoxin antibodies. Antibodies come from blood donors who have recently had the tetanus vaccination. Only provides short term protection as abs destroyed by phagocytes in spleen and liver.

Active and Passive Immunity Natural passive immunity A mother’s antibodies pass across the placenta to the foetus and remain for several months. Colostrum (the first breast milk) contains lots of IgA which remain on surface of the baby’s gut wall and pass into blood