immunology

Cards (36)

  • Pathogenic
    An organism that causes damage to its host
  • Infectious
    A disease that may be transmitted from one individual to another
  • Carrier
    Shows no symptoms when infected but can pass the disease on to another
  • Disease reservoir
    Where a pathogen is normally found; this may be in humans or another animal and may be a source of infection
  • Endemic
    A disease, which is always present at low levels in an area
  • Epidemic
    Where there is a significant increase in the usual number of cases of a disease, often associated with a rapid spread
  • Pandemic
    A global epidemic
  • Vaccine
    Uses non-pathogenic forms, products or antigens of micro-organisms to stimulate an immune response, which confers protection against subsequent infection
  • Antibiotic
    Substances produced by microorganisms that affect the growth of other microorganisms
  • Antibiotic resistance
    Where a microorganism, which should be affected by an antibiotic, is no longer susceptible to it
  • Antigen
    A molecule that causes an immune response
  • Antibody
    A protein produced by the immune system to recognise and destroy antigens
  • Vector
    A living organism which transfers a disease from one individual to another
  • Toxin
    A chemical produced by a microorganism, which causes damage to its host
  • Antigenic type
    Organisms with the same or very similar antigens on the surface. Such types are subgroups or strains of a microbial species, which may be used to trace infections. They are usually identified by using antibodies from serum
  • Viral diseases

    1. Viral DNA/RNA instructs the cell to make virus particles, when full cell lysis occurs, and the virus escapes the cells to infect other cells/organisms (shedding)
    2. Production of toxic substances
    3. Viral cell transformation, where they can trigger cells to become cancerous
    4. Viruses infecting white blood cells suppress the immune system (e.g. HIV)
  • Gram negative bacteria
    Have a thin peptidoglycan cell wall with a layer of lipopolysaccharide. Gram negative bacteria stain red using Gram staining technique. The additional layer of lipopolysaccharide protects the bacterial cells from lysozyme and from penicillin type antibiotics
  • Gram positive bacteria
    Have a thick peptidoglycan cell wall and no lipopolysaccharide layer. Gram positive bacteria stain purple using Gram staining technique. Gram positive bacteria are susceptible to lysozyme and penicillin
  • Body defences
    • Skin
    • Lysozyme
    • Ciliated mucous membranes
    • Blood clotting
    • Inflammation
    • Blood - white blood cells called phagocytes kill invading microbes in a process called phagocytosis
    • Antibodies
  • Antibodies
    These are produced by white blood cells called lymphocytes. Antibodies are proteins (globulins). They are Y shaped and formed from four polypeptide chains with two binding sites. They are specific to the antigen and they bind to form an antigen-antibody complex. This renders the antigen inactive by agglutination or marking for phagocytosis
  • Antibiotic resistance
    1. Bacteria divide rapidly and have a high mutation rate. Bacteria can also obtain plasmids that carry antibiotic resistance genes from other resistant bacteria by conjugation
    2. Some mutations confer resistance to antibiotics. Overuse of these antibiotics gives the resistant strain a selective advantage
    3. Numbers of the resistant strain increase, making infections more difficult to treat with the usual antibiotics
  • Penicillin
    Peptidoglycan bacterial cell walls are strengthened by polysaccharide cross-linked by amino acids. This stops osmotic lysis. Penicillin affects the formation of the cross links by inhibiting the enzyme that makes them. The wall is weakened and osmotic changes can cause cells to burst. Gram negative bacteria have an outer lipopolysaccharide layer that protects the cells from penicillin
  • Tetracycline
    Tetracycline acts as a competitive inhibitor of the second anticodon-binding site on the 30S subunit of bacterial ribosomes. It prevents the binding of a tRNA molecule to its complementary codon. This prevents protein synthesis common to all bacteria
  • Humoral immune response
    1. Stem cells in the bone marrow make B lymphocytes that mature in the spleen and lymph nodes and have receptors for the detection of specific antigens on the surface of foreign cells
    2. When the B lymphocytes are activated by a corresponding antigen, they divide rapidly forming antibody secreting plasma cells. This clonal expansion is increased by the cytokines from the cell mediated response
    3. B lymphocytes also make memory cells that remain in the bloodstream and divide rapidly if the antigen is encountered again
  • Primary immune response
    1. On first exposure to the antigen, there is a latent period when antigen presenting cells (including macrophages) carry out phagocytosis and incorporate foreign antigen into their cell membranes (antigen presentation)
    2. T helper cells detect these antigens and secrete cytokines that stimulate B cells to undergo clonal expansion and stimulate macrophages to carry out phagocytosis
    3. Some B cells then differentiate to become antibody-secreting plasma cells with short lives. Others become long-lived memory cells that retain the ability to undergo mitosis in case of secondary infection
  • Secondary immune response
    1. Following re-exposure to the same antigen, there is a very short latent period due to the presence of memory cells
    2. Only a very small amount of antigen is required to stimulate rapid production of plasma cells
    3. Antibody levels increase to between 10 and 100 times greater than the initial response in a very short time frame. Antibody levels stay high for longer and no symptoms develop
  • Vaccinations
    • A vaccination stimulates artificial active immunity in an individual
    • A vaccine must contain an immunogenic antigen that stimulates a strong immune response
    • Vaccinations for pathogens that exhibit low levels of antigenic variation can protect an organism after one immunisation, e.g. Rubella
    • Some pathogens have many antigenic types and mutate frequently. These require seasonally repeated immunisations
  • Immunisation programmes considerations
    • Cost vs effectiveness of the vaccine
    • Protection of the individual compared to protection of the community
    • The rights of the individual when considering mandatory or voluntary programmes
    • Side effects
  • Active immunity
    Individual produces antibodies. Protection is long lasting due to production of antigen specific memory cells
  • Passive immunity
    Individual receives antibodies from someone else. Protection is short lived as no memory cells are produced and the antibodies themselves identified as foreign and destroyed
  • Cell mediated immune response
    1. Stem cells in the bone marrow make T lymphocytes, which are activated in the thymus gland
    2. Detecting a foreign antigen causes proliferation of T lymphocytes as: T killer cells cause lysis of target cells, T memory cells remain in bloodstream, T helper cells release cytokines
    3. Cytokines stimulate the clonal expansion of B cells and to produce antibodies. Cytokines activate phagocytes to engulf and digest the foreign cells
  • disease - cholera
    causative agent - gram negative bacteria
    tissue affected - gut lining causing watery diarrhoea leading to dehydration and death
    mode of transmission - water
    control methods and treatment - water treatment, rehydration therapy, antibiotics, vaccine
  • disease - tuberculosis
    causative agent - bacteria
    tissue affected - lungs, neck and lymph nodes. causes coughing, chest pains, coughing up blood
    mode of transmission - airborne droplets through coughs and sneezes
    control methods and treatment - antibiotics + vaccination
  • disease - smallpox
    causative agent - variola major virus
    tissue affected - mouth, throat, lymph nodes, blood stream.
    mode of transmission - contact, person to person or from contaminated objects
    control methods and treatment - low antigenetic variation of the virus led to a highly effective vaccine.
  • disease - influenza
    causative agent - virus
    tissue affected - lining of upper respiratory tract leading to sore throat, coughing and fever
    mode of transmission - airborne droplet infection
    control methods and treatment - quarantine and hygiene, annual vaccination - not always effective
  • disease - malaria
    causative agent - proctoctistan parasite
    tissue affected - liver and red blood cells
    mode of transmission - vector, passed to humans by mosquito when feeding
    control methods and treatment - stop the vector - nets, clothing, insect repellent. kill parasite - drugs