* Body defence mechanism (Ch 24) Flashcards
First line of defense: Physical barriers
- Skin
- Hair at nostril
- Musus secreting cells and ciliated epithelial cells of respiratory tract
- Mucus secreting cells secrete mucus to trap germs / pathogens / bacteria from incoming air. Beating action of cilia sweeps the trapped pathogens away to the pharynx for swallowing to stomach or coughing. - Blood clotting
- Damaged cells and blood platelets release clotting factors, which brings about the formation of an activated enzyme. The activated enzyme catalyses the conversion of fibrinogen into fibrin, which forms a network entangling red blood cells, white blood cells, platelets and pathogens to form clot blocking up the injured sites of the blood vessel
- Prevent further bleeding
- Prevent invasion of pathogens through the wound
First line of defence: Chemical barriers
- Tear: contains lysozyme to kill the pathogens, helps wash away the pathogens from the conjunctiva
- Saliva: contains lysozyme to kill the pathogens
- Sebum: contains antiseptic which inhibit the growth of pathogens
- Sweat
- Gastric juice: contains hydrochloric acid which kills pathogens entered the stomach with food
- Vaginal secretions: contains acidic substances to inhibit the growth of pathogens in vagina
Second line of defence
- Phagocytosis
- When the skin is damaged and pathogens entered the body, phagocytes squeeze through the capillary wall and engulf the pathogens - Inflammatory response
- Red: arterioles of the tissue with inflammatory response dilate, increasing blood flow to the tissue and makes it red
- Hot: high metabolic activity, produces more heat / caused by extra blood flow to inflamed area and blood carries heat
- Swelling: permeability of capillary wall increases, increasing the rate of formation of tissue fluid. When the rate of tissue fluid formation is higher than the rate of tissue fluid draining away, accumulation of tissue fluid at the infected site causes swelling
- Pain: accumulation of tissue fluid presses against nerve endings, stimulating pain receptors and gives pain sensation
- Increased blood flow and permeability of blood capillaries allow more phagocytes to reach the infected area to engulf and kill invading pathogens
- Antimicrobial proteins
- Fever
- Fever increases body temperatures to activate proteins involving in body defence and suppress microbial growth and propagation
Sub-cellular structure of phagocytes for phagocytosis
- Lysozyme: to kill the pathogens
- Mitochondria: provide energy for synthesis of protein
- Rough endoplasmic reticulum: synthesis of lysozyme
- Glycoprotein on cell membrane: recognize pathogen
- Fluid nature of cell membrane: to engulf pathogens
Antigen
- Some surface molecules with specific shape, which are recognized as foreign and stimulate an immune response
Lymphocytes production, maturation, storage
B cells
- Production: bone marrow
- Maturation: bone marrow
T cells
- Production: bone marrow
- Maturation: thymus
Both storage: lymph nodes and spleen
B cell immune response
- When antigen on the surface of pathogen bind to the receptor site of B cell, the binding stimulates the B cell to proliferate and differentiate into plasma cells. The plasma cell then form a large number of antibodies to combat against the pathogen
*Plasma cells have large number of rough ER and mitochondria for active production of antibodies
*No B cells without helper T cells
- Some B cells proliferate and differentiate into memory B cells when they encounter the antigen of the pathogen for the first time. When the same pathogen invades the body, it will be recognized by the memory B cells, which will proliferate and differentiate into plasma cells rapidly, resulting in the production of large number of antibodies within a short time to act against the pathogen
Action of antibodies
- Antibodies indirectly cause lysis of pathogens through binding on them. This attracts certain proteins in blood to cause lysis of the pathogens
- Antibodies attach to the antigens on the surface of pathogens. Antibodies bind to several pathogens together as a clump to enhance the phagocytosis by phagocyte
- Act as antitoxins which binds to the toxins secreted by bacteria. This makes the toxins harmless
T cells
- Antigens of pathogens stimulates T cells to proliferate and differentiate
- Killer T cells kills the infected cells directly
- Helper T cells secrete lymphokines to stimulate B cells to proliferate and differentiate into plasma cells to produce antibodies / activate T cells to proliferate and differentiate into killer T cells and memory T cells / activate phagocyte to engulf pathogens
- Memory T cells: when the same type of antigen invades the body again, memory T cell formed during the first exposure to the antigen will proliferate and differentiate rapidly to form a large number of killer T cells within a short period to time to kill the infected cells
Relationship between phagocytosis and specific immune responses
- After phagocytosis, the antigens of pathogens will be broken down intracellularly. The antigens will be presented to the lymphocytes for recognition. This elicits specific immune responses
- Activated helper T cells liberate chemicals to activate phagocytosis.
- Antibodies cause clumping of pathogens which make them more easily to be phagocytosed
Limitations of body defence mechanism
- Mosquitoes with piercing mouthparts break the integrity of the skin
- Pathogens can mutate, thus not recognized by memory B and T cells to elicit secondary response
- Delayed response allows pathogens to multiply
- Hyperstimulation of immune system kill our own body cells
Primary vs Secondary response
Primary response: quicker decrease in level of antibodies
- Antibodies are used up
- Plasma cells degenerate
Immunity
Active immunity
- Antibodies produced by oneself
- Memory cells produced
- Natural: recovery from a disease
- Artificial: vaccination
Passive immunity
- Antibodies received from others
- Natural: antibodies in maternal blood pass through the placenta and enter into the foetal blood / maternal antibodies in mother’s milk pass to the newborn through breast feeding
- Artificial: injection of antibodies
Principle of vaccination
- During the first injection, as the vaccine contains antigens, it stimulate B cells to proliferate and differentiate into memory B cells. When the same antigen invades the body again, the antigen will be recognized by memory B cells which proliferate and differentiate into plasma cells rapidly, resulting in the production of a large amount of antibodies within a short period of time to act against the pathogen, leading to a sharp rise in the protection against the infection
Side effects of vaccination
- Pain in injection site
- Headache
- Fatigue