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Primary immune response
first time we are exposed to a specific antigen, B cells are activated and undergo clonal selection
B cell clones become plasma B cells (make antibodies) and memory B cells (stay in body forever)
the first exposure you will get sick and experience symptoms of whatever the antigen is.
Secondary immune response
future exposure to the same antigen, we already have memory B/T cells in the body that mount faster and more efficient attack
gets rid of antigen quickly so we don’t get sick (no symptoms)
antibody structure/function
antibody molecules are made by plasma B cells
they are specific to the antigen in question
antibodys are protein molecules also called immuglobulins
5 classes of immunoglobulins
IgG
IgE
IgA
IgD
IgM
Antibody structure
Y shaped model
variable regions: thicker
constant regions: thinner
Variable regions
ability to change depending on specific antigen
the 2 antigen binding sites are at the variable regions because they need to be able to change
each antibody molecule has 2 antigen binding sites - so it can bind to 2 antigens
4 different ways the antibodies can destroy or incapacitate/inactivate antigens
P: Precipitation
L: lysis
A: agglutination
N: neutralization
P: percipiation
antibody binds to the antigen and its complex is so heavy when binded together that it precipitates (sinks) which incapacitates antigen
L: lysis
most common way antibodies work
antibody binds to antigen and activates the complement system which causes lysisor destruction of antigen
A: agglutination
antibody binds to antigens and complexes get stuck together and clump which incapacitates the antigen
N: neutralization:
the antibody binds to the antigen and neutralizes/inactivates it
Active immunity
being exposed to pathogen/antigen
going though that whole process, making antibodies and memory B/T cells
Active immunity (naturally acquired)
when we are exposed to pathogens in our environment we make antibodies and memory cells
we get sick (get symptoms)
Active immunity (Artificially acquired)
vaccinations
when we expose the body to a dead or weakened pathogen (nasal spray), we trick the body into making antibodies (memory B cells)
we don’t get sick/symptoms
Passive immunity
protection from pathogens/antigens
provided by antibodies that are from another source (no memory cells produced)
temporary - short lived
Passive immunity (naturally acquired)
mom can pass her antibodies to her fetus across the placenta so the fetus is protected
mom can pass her antibodies to her baby through breast feeding
Passive immunity (artificially acquired)
antibiotic medications for bacteria/antivenins
cell mediated response:
activation of T-lymphocytes by antigen presenter cell
T cells are presented with the antigen by an antigen presenter cell, and this activated the T-cell- T cells undergo clonal selection and makes and army of T cell clones
5 different T cells
Cytotoxic (killer) T cells
have ability to directly attack virus infected/tumor cells
only T cells that can directly attack/destroy
destroy cells by releasing cytotoxic chemicals
Helper T cell (CD4)
managers of immune system
give immune system momentum (ramp up to full speed)
recruit/activate other immune cells
HIV virus attacks these cells
supressor T cells
we need these cells to suppress immune system activity once the pathogen has been destroyed
Delayed hypersensitivity (allergies) T cells
Help manage delayed hypersensitivity
allergies to poison ivy/metals/detergents/lotions
Memory T cells
stay in the body forever and mount a stronger, faster, more efficient response to secondary exposure
Antigen presenter cells
macrophages
engulf the antigen in question, destroy that antigen, and display the antigen fragments on the surface of the macrophages
this macrophage is going to entirely engulf that antigen and break it apart into little pieces and display those pieces on its surface
then presents the antigen to the T cell and activated it