The body's defense mechanisms
I. Targets of the body's defense mechanisms
A. Pathogens -- disease causing organisms
- bacteria
- viruses
- protozoa
- fungi
- parasitic worms
1. bacteria
- prokaryotes
- cell wall
- reproduce asexually -- on average every 20 minutes
- disease producing agent: toxins
- antibiotics kill bacteria
- directly -- cause lysis
- slow growth
- prevent synthesis of cell wall
- prevent synthesis of bacterial proteins
2. viruses
- strand of DNA or RNA surrounded by protein coat
- life cycle:
- bind to cell via receptor
- virus enters cell/injects genetic material
- uses host cell machinery to:
- replicate its DNA
- direct synthesis of protein coat
- thus new viruses quickly form
- may insert genetic material into chromosome of host cell
- disease:
- destruction of host cell
- insert genetic material next to host cell proto-oncogene -- cancer
3. Protozoa
- single-celled organisms
- disease:
- toxin production
- release of enzymes that prevent cells of host from working properly
- examples:
4. Fungi
- single cells, simple multicellular organisms
- examples:
- histoplasmosis -- lung infection
- athlete's foot
5. Parasitic worms
- multicellular organisms
- examples:
- flutes
- tapeworms
- pinworms
- disease:
- release toxins
- competition
B. Cancerous cells
- genetic changes
- cannot regulate cell cycle
II. Body's defenses -- non-specific mechanisms
- provide barriers that keep substances from entering body
- limit spread of pathogens that break barrier
1. surface barriers
- skin
- epidermis with keratin
- chemical protection of sebum
- mucous membranes
- line inner body cavities
- physical defenses:
- chemical defenses:
- high acidity -- vagina, urethra
- anti-bacterial secretions -- lysozyme
2. phagocytic cells
- scavenger cells that specialize to engulf and destroy particulate matter
- front-line defense
- neutrophils
- eosinophils
- monocytes -- macrophages
3. natural killer cells (NK cells)
- cells that roam body in search of "suspicious characters"
- cancerous cells usually target
4. defensive proteins
- proteins in plasma that are anti-microbial
a. interferons
- proteins released by cells infected by viruses before they die
- attract macrophages and NK cells
- will protect cells not yet attracted by virus
- causes these cells to produce proteins that inhibit viral replication
- thus protects cells from all strains of viruses
- effective against some cancers (certain types of leukemia) and
infections (hepatitis C)
b. complement
- group of about twenty proteins usually found in blood
- activated to become anti-microbial in two ways:
- antibody binding
- proteins in coats of bacteria/viruses/infected cells
- series of reactions occur that punch holes in membrane of pathogen
- clusters form -- macrophages attracted
5. Inflammatory reaction
- a nonspecific response of body to injury or invasion by foreign organisms
- four cardinal signs:
- redness
- swelling
- heat
- pain
- progression outline:
- basophils/mast cells at site of injury release chemicals
- attract neutrophils, macrophages
- increase permeability of capillaries -- swelling
- cause blood vessels to widen -- heat, redness
- neutrophils arrive
- remove microbes, die
- pus formed
- macrophages clean up mess
6. fever
- elevated body temperature
- caused by pyrogens
- from bugs
- from macrophages
- pyrogens
- raise body temperature set point
- set point floats back down
- sweating to dissipate heat
- how does fever help?
- increases neutrophil activity
- interferons work better
- microbes don't reproduce as well
- immune system more efficient
III. Body's defenses -- the immune system
A. General characteristics
- acts on specific targets
- zero on pathogens and eliminate them
- immunological memory
- systemic response
- not limited to initial infection site
- recognition of self from non-self
B. Terminology
- antigen
- molecule of part of molecule usually found on the surface of pathogens
- recognized by lymphocytes as non-self
- lymphocytes -- cells of specific defense
- B-cells -- mature (immunocompetent) in bone marrow
- make antibodies
- antigen presentation
- T-cells -- mature (immunocompetent) in thymus
- cytotoxic T-cells
- helper T-cells
- found in lymph nodes, spleen, secondary lymphoid organs
- macrophages -- antigen presentation
- MHC complex
- markers of self
- windows to the cell
- concept of antigen presentation
C. The cell mediated immune response
1. T-cells immunocompetent in thymus
- helper T-cells
- cytotoxic T-cells
2. Infection -- pathogen in lymphatic system/blood
- virus example -- specific body cells infected
- viral antigens incorporated into MHC complex
- virgin cytotoxic T-cell binds self/nonself complex
- macrophage engulfs viruses
- viral antigens presented on macrophage MHC complex
- virgin helper T-cell binds macrophage MHC complex
- macrophage releases IL-1
- IL-1activates helper T
- divides into effector helper T and memory helper T
- effector helper T secretes IL-2
- IL-2 activates primed cytotoxic T
- primed cytotoxic T becomes effector cytotoxic T
- divides into more effector cytotoxic T
- destroys infected cells -- perforins
- divides into cytotoxic memory T
D. Antibody-mediated response
- infection -- virus example
- virgin B-cell (lymph node, spleen) binds antigen
- virgin B-cell primed
- processes bound antigen, presents it as part of MHC complex
- primed B activated only if
- stimulated by IL-2 release
- binds helper T-cell that recognizes specific self/nonself complex
- activated B cell divides
- effector B cells -- plasma cells
- make antibodies to that antigen
- memory cells
E. Immunological memory
- the body's capacity to make a quicker and more intense immune
response to any subsequent encounter with the same type of antigen that provoked
the primary response
- memory cells formed during a primary response do not engage in battle
- quickly activated into effector cells and more memory cells upon susequent
exposure to same antigen
F. Immunoglobulins
- mechanism of antibody action
- neutralization
- agglutination
- precipitation
- activate complement
G. Types of acquired immunity
- naturally acquired
- artificially acquired