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Two Major divisions of immune system
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Specific
- Fight off specific pathogens by protein to protein interactions
- Allows us to become to immune to future infections by memory cells
- B&T cells
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Non Specific
- Defenses that are used to fight off infection in general
- Ex: Skin and mucous
- Skin will not let bacteria or viruses through unless it is penetrated
- Sweat and oil give skin a pH of 3-5 and discourage bacteria and microbes
- Mucous traps foreign particles and that are either coughed up or swallowed and digested by the stomach
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Lysozyme
Enzyme in saliva tears and mucous that destroys bacteria cells walls causing them to lyse
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Macrophages
Large while blood cells that circulate looking foreign material to engulf via phagocytosis
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Monocytes
Macrophages name when they are circulating the blood and are able to transport themselves through capillaries into infected tissue
Once in tissues knowns are macrophages
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Psuedopedia
- used to pull in foreign particles to destroy them with lysosomes
- use actin and mysosin to make (feet) and put in particles
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Antigen Presenting Cells (APC)
- Ex: macrophages
- They have the ability to display antigens they engulfed on their cell surface so that they can be recognized by T cells
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Neutrophils
White blood cells that use phagocytosis but are not APC's
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Histamine
- Responsible for dialating the walls of capillaries, allowing macrophages and neutrophils to enter more easily
- Resleased by basophils, and mast cells
- Increases blood flow to area, and results in redness and heat of injury
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Cytokines
- Chemicals the excite specific immune defenses to activate
- Released by basophils and mast cells
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Lymphocytes
Major defense used by specific system, B&T cells
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B cells
Are produced in bone marrow and mature here and in spleen
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T Cells
- Are produced in bone marrow and mature in thymus
- Cannot detect free antigens only those displayed on macrophages
- Direct killing and overall activation of the immune system
- Basis for cell mediated immunity
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Thymus
Essential for educating T cells to recognize self antigens (and therefore those that are not self)
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Three types of T cells
- Helper T cells
- Cytoxic T cells
- Suppressor T cells
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Cytotoxic T cells: Tc
- Killer T Cells
- Essential against viruse
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Suppressor T cells: Ts
Involved in controlling the immune response so it doesn't run out of control by suppressing antibodies produced by B cells
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Helper T cells : Th
- Secrete chemicals to help B cells proliferate
- Helper T cells can bind to molecules displayed by MCH II like macrophages and this binding triggers immune system to make antibodies
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B Cells
- Make up 30% of lymphocytes are specific for foreign antibodies by Y shaped receptors
- Secrete antibodies
- Basis for humoral or fluid immunity
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Immunoglobulins
Antibodies that are produced solely by B cells, B cell can produce any class of immunoglobulins
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5 Classes of Antibodies
- IgG
- IgD
- IgM
- IgE
- IgA
- All Immunoglobin (then letter)
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Paratrope
- Antigen binding site
- Formed for one variable Heavy and one variable light chain
- Each antibody has two
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Light and Heavy Chains
- Similar in amino acids but Heavy is longer
- Involved in antibody diversity
- Heavy chain is 5'VDJC3'
- Light chain is 5'VJC3'
- There are hundreds of V's, dozens of D's and 4-5 J's and C is a constant group
- They get spiced together to form a unique antibody amino acid sequence
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IgG
Found in phagocytic cells
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IgM
Secreted into the blood as primary immune response
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IgD
Found on B cells they bind antigens together
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IgA
are in salvia milk and respiratory secretions
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IgE
- Found on most cells and elsewhere
- Are precursors to allergic reactions by releasing histamine
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Agglutination/ Neutraization
Antibodies cross link adjacent antigen molecules so that invaders get stuck together by antibodies and are engulfed by macrophage
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Precipitation
Similar to agglutination but for soluble antigen molecules like small bacterial toxins
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Complement Activation
antibodies bound to foreign cells activate the 20 complement proteins that are turned on in a cascade lie fashion
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Opsonization
- Coating of a foreign cell with antibodies
- Stimulates Macrophages to engulf and digest these invaders
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Classic Pathway to Complement Activation
- Requires antibodies to bind to antigens
- Complement proteins bridge the cap between adjacent antibody molecules
- Lyse the cell membrane of invader
- Also activated mast cells to release histamine
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Aclassical Pathway of Complement Activation
- Occurs independantly of antigen-antibody binding
- Cell surface molecules of antigen can cause cell membrane attack complex without the help of antibodies
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Polyclonal
- Antibodies that arise in natural course of fighting pathogens
- But from several clones of B ells and cover a wide range of specificity
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Monoclonal
Antibodies that arise from a single clone of a single B Cell
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Lag Period
- The period after exposure to a pathogen but before enough B cels have been made
- APC's like macrophages process and display antigens to ThCells
- Th Cells activate B cells to form antibodies
- First exposure lag period is usually 7-10 days
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Secondary Response
Second time a person is exposed to an antigen lag period is much shorter (1-4 days) and anitbodies are typically greater in number than they were at first response
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Memory Cells
- Specific antibody cells that remain after infection
- Memory B&T cells live for decades
- Basis of immunity and form concept behind vaccinations
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MHC - Major HIstocompatibility
- Surface cell proteins used in tissue typing
- MCH 1 displays a small bit of cellular contents on surface of cells, allows for killer T cells to monitor cells contents
- Cannot distinguish between self and antigen so grabs a bit of both and displays both on surface
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MCH I
- MCH 1 displays a small bit of cellular contents on surface of cells
- allows for killer T cells to monitor cells contentsCannot distinguish between self and antigen so grabs a bit of both and displays both on surface
- Killer T cells recognizes antigen and kills it
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MCH II
- Only found in macrophages and B cells
- Allows cells to display a bit of whatever they ingested through phagocytosis
- Helper T cells can bind to molecules displayed by MCH II and this binding triggers immune system to make antibodies
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