Immunology and Lab Techniques Flashcards
(26 cards)
thymus
produces t cells
lymph nodes
storage houses that trap pathogens
spleen
filters blood
bone marrow
makes b cells
antigens
non-self, stimulates an immune response
humoral immune response
has memory and is specific
huMmoral : m for memory
antibodies and b cells
innate immunity
nonspecific response
Innate immunity first line of response
physical barriers: stomach acid, skin, mucus membranes
innate immunity second line of defense
white blood cells!
phagocytes, NK cells, cytokine cascade
why are people getting bone marrow transplants susceptible to infection
compromising b cell production
\
t cell role
gives a signal to the white blood cells to come and attack
immunogloblins
antibodies
igM
first antibody to get made in an infection, made by fetus and b cells
igG
secondary one made, gives lasting protection, has memory so can give robust response among the second exposure, can be transferred through the placenta
after infection the concentration never drops back down to 0
igA
secretory Ig,
tears, saliva, gastric and pulmonary secretions
IgE
allergic reactions and parasitic infections
IgD
on the surface of B cells
naive
no protection against the antigen
cultures
the gold standard, growing the pathogen outside of the host
lab techniques that detect antigens and antibodies
LA (latex agglutnation), complement fixation (CF), enzyme linked immuno-assay (ELA), fluorescent antibody (FA)
ELISA
attach antibody onto a plate, take blood serum, and if the person has the antigen it will stick to the antibody.
then add another MARKED antibody that will stick to the antigen, wash, and then we can visualize the tagged antibodies.
titer
quantifies the circulating levels of antibodies in the body, measured by the DILUTION of the serum sample
paired sera
four fold increase between acute and convalescent sera to show recent infection
We can take 2 sera draws from someone, we can tell if they have an old or a new infection
Each of the lines marks when the person’s blood was drawn.
For example, we do it first at day 3 for igm, and then draw again at the peak of the infection, we draw again at the peak of the infection. We want to see a 4 fold increase in the two titers.
Molecular techniques
use RNA and DNA
quick, highly sensitive, initially expensive