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Examen

MICR 3230 MIDTERM | UPDATED Questions with 100% Verified Answers

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Vista previa 4 fuera de 38 páginas

MICR 3230 MIDTERM | UPDATED Questions with 100% Verified Answers

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MICR 3230 MIDTERM | UPDATED Questions with 100% Verified
Answers

Question:
immunity

Answer:
state of protection against foreign pathogens or substances (antigens)
can generate immunity without inducing disease (through vaccine)


Question:
herd immunity

Answer:
acquiring protective immunity in a critical mass of people through vaccination or
recovery from infection
serves as a buffer for everyone else


Question:
humoral immunity

Answer:
soluble proteins for labelling and destruction of invaders
combats pathogens via antibodies produced by B cells


Question:
cell mediated immunity

Answer:
cells that recognize and kill or engulf pathogen
involves primarily T cells
eradicate pathogens, clear infected self cells, or aid other cells in inducing immunity


Question:
important concepts for understanding the mammalian immune
response

Answer:

,humoral and cell mediated immunity relies on surface receptors (B and T cell receptors)
receptors are randomly generated by gene segment rearrangements in B and T cells
B cells that encounter an antigen produce an antibody specific to the antigen
T cell receptors bind antigens or specific peptides presented by antigen presenting cells


Question:
4 main categories of pathogens

Answer:
viruses
bacteria
fungi
parasites


Question:
pathogen recognition

Answer:
interaction bw foreign organisms and recognition molecule expressed by host cells


Question:
ligands

Answer:
include whole pathogens, antigenic fragments of pathogens, or products secreted by
foreign organisms


Question:
ligand binding outcome

Answer:
extra or intra cellular cascade of events leading to labelling and destruction of pathogen
(immune response)


Question:
immune response relies on

Answer:

,recognition molecules
- encoded in genomic DNA and always expressed
- PRRs which bind to PAMPs
- randomly generated (B and T cell receptors)


Question:
colonial selection and generation of diversity

Answer:
individual B and T cells each have an individual specificity for a single antigen
- due to each cell having many copies of a receptor on the surface that only binds to one
type of antigen
when a B or T cell interacts w its specific antigen, it is selected and becomes activated
- activation results in proliferation, producing a large # of clones
- each clone is reactive against the antigen that initially stimulated the original
lymphocyte


Question:
tolerance

Answer:
ensures that the immune system avoids destroying host tissue (self/non-self
discrimination)
many of the random rearrangements used to create B and T cell receptors could be anti-
self
Tolerance helps to keep these anti-self recognition molecules/cells from circulating in
the bloodstream
self tolerance prohibits immune responses to host tissue maintained through elimination
or inhibition of cells


Question:
vertebrae immune system uses two interconnected systems:

Answer:
innate and adaptive immunity


Question:

, innate immune response

Answer:
first line of defence
- fast but non specific
uses inherited recognition molecules
also uses phagocytic cells


Question:
adaptive immune response

Answer:
humoral and cell mediated responses
- using B and T lymphocytes
- slower to develop (5-6 days or more)
- use randomly generated antigen receptors
- highly specific to individual antigen molecules


Question:
innate and adaptive immune systems both work...

Answer:
cooperatively
activation of innate immune response produce signal molecules (cytokines, chemokines)
signal molecules stimulate and direct adaptive immune responses


Question:
memory

Answer:
hallmark of adaptive immunity
primary response is initiated upon first exposure to an antigen
- memory lymphocytes are left behind after antigen is cleared
secondary response is initiated upon secondary exposure to the same antigen that
stimulate memory lymphocytes
- stimulation yields faster, more significant, better response
memory is NOT present in innate immunity

Información del documento

Subido en
21 de septiembre de 2026
Número de páginas
38
Escrito en
2026/2027
Tipo
Examen
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