• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/95

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

95 Cards in this Set

  • Front
  • Back
Chapter 1 Introduction to the Immune System
Chapter 1 Introduction to the Immune System
immunity
resistance to infectious disease
collection of cells tissues and molecules that mediate resistance to infection
immune system
coordinated reaction of immune system to infectious microbes
immune response
study of immune system
immunology
most important physiologic function of immune system
prevent infections, eradicate established infections
most effective method for protecting individuals against infections
vaccination
other role of immune responses besides infections
defense against tumors, healing, clearance of dead cells
major barrier to sucessful organ transplantation
immune response
mediates the initial protection against infections
innate immunity
provides specialized and effective defense against over time
adaptive immunity
adaptive immunity requires
expansion and differentiation of lymphocytes in response to microbes
first line of defense in innate immunity
provided by epithelial barriers and cells with natural antibiotic in epithelia
innate immune response once barrier is breached
NK cells, phagocytes, and complement system
adaptive immunity consists of
lymphocytes and their products (ie: antibodies)
molecules produced by microbes and noninfectious substances
antigens
two types of adaptive immunity
humoral and cell mediated
humioral immunity mediated by
antibodies produced by B lymphocytes
antibodies cannot gain access to these microbes
those that live and divide inside infected cells
defense against intracellular microbes is called
cell mediated immunity
main cell of cell mediated immunity
T lmyphocyte
active immunity
immunity induced by infection or vaccination
passive immunity
immunity confered by transfer of antibodies or lymphocyres from actively immunized individual
benefit and limitation to passive immunity
rapid conference of immunity before the body would be able to do so BUT this is not long lived
physiologic example of passive immunity
mother to baby through placenta and breast milk
specificity ensures
distinct antigens elicit responses that target those antigens
diversity enables
immune system to respond to a large variety of antigens
memory leads to
rapid/enhanced responses to repeated exposures to same antigen
clonal expansion
increases # of ANTIGEN SPECIFIC lymphocytes to keep up with microbes
contraction/homesostasis
allows immune system to respond to newly encountered antigens
nonreactivity to self
preventsinjury to host during response to foreign antigens
lymphocyte repertoire is extremely
diverse
clonal selection hypothesis
clones of lymphocytes develop for specific antigens and each antigen will elicit a response by selecting for and activing the lymphocytes of a specific clone
response to first exposure to antigen
primary immune response
subsaquent exposures to antigens mount a
secondary immune response , more rapid and larger
optomizes ability of immune system to combat persistant and recurrent infections
immunologic memory
immunological tolerance
body usually does not respond to self antigens
only cells that produce receptors specific for diverse antigens
lymphocytes
CD
cluster of differentiation. CD proteins are surface proteins that are used to differentiating between immune cell types
only cells capable of producing antibodies
B cells
most T cells recognize only these antigens
fragments displayed on MHC molecules
why are helper T cells called such
they help B lymphocytes produce antibodies and help phagocytes destroy ingested microbes
CD8+ T cell
cytotoxic T cells, kill cells harboring intracellular microbes
NK cells
specialized lymphocytes that are capable of rapidly attacking infected cells. Part of innate immune system
B cells arise where
bone marrow
T cells arise where
bone marrow
T cells mature where
thymus
all lymphocytes arrise from
stem cells in bone marrow
generative lymphoid organs
sites where mature lymphocytes are produced
peripheral lymphoid organs
site where mature lymphocytes are found in addition to bloodstream
display antigens to B lymphocytes in humoral immune responses
follicular dendritic cells
effector phase of cell mediated immunity
macrophages
initiation of T cell responses
dendritic cells
granulocytes
neutrophils and eosinophils
mononuclear phagocytes
macrophaes and monocytes
when niave lymphocytes recognize antigen what happens
activated and proliferate / differentiate into effector and memory cells
niave lymphocyte
express receptor for antigen but do not perform function required to clear antigens
niave lymphocytes reside
peripheral lymphoid organs
how long do niave lymphocytes live if unactivated
weeks to months then apoptosis and replenishment
progeny of niave cells with ability to produce molecules that elimnate antigens
effector cells
effector cels of B lymphocyte lineage
plasma cells
plasmablasts
antibody producing cell
effector CD4+ cells produce
cytokines that activate other cell types
effector CD8+ cells
have machinery to kill infected host cells
memory cells
generated from progeny of antigen stimulated lymphocytes have ability to survive for long time in absense of antigen
APCs are usually located where
at areas that are common portals of entry for microbes
dendritic cells
capture antigens of microbia in epithelia and transport them to lymphnodes for recognition by T lmyphocytes
most effective APC for initiating T cell responses
dendritic cells
follicular dendritic cells reside where
germinal centers of lymphoid follicles ; displays antigens that stimulate differentiation of B cells in follicles
macrophage response: innate and active response
macrophages innately act as effector cells but can be recruited and activated by specific active immune responses
peripheral lymphoid organs include
lymph nodes spleen and mucosal/cutaneous systems
benefit of peripheral lymphoid organs
allows for concentration of antigens. Remember only ~1-10k lymphocytes for any 1 antigen. Imposisble for so few cells to patrol whole body for specific antigen, rather lymph flow bring the antigens to them at said peripheral lymphoid organs and dendritic cells can present antigens as well
encapsulated nodular aggregate of lymphoid tissue
specialized lymphocytes that are capable of rapidly attacking infected cells. Part of innate immune system
really simple explanation of spleen
filters blood for antigens the same way a lymph node filters lymph for antigens
cutaneous and mucosal immune system act simmilar to
lymph nodes
examples of cutaneous and mucosal immune system
tonsils, peyers patches
in lymph node where are B cells
within follicles located
if B cells are responding to an antigen in a lymph node, how will the node appear
will have a germinal center
where are T cells in lymph node
outside but adjacent to follicles
FDC's in the follicles produce this which is a chemokine for B cells
CXCR5
T cells are located in areas of high amounts of this chemokine
CCR7
causes T/B cells to meet following antigen exposure
altered chemokine activity
where do effector T cells go
from peripheral lymphoid organ to sites of infeciton
why is it less important for effector B cells (plasma) to migrate to site of infection
they secrete antibodies which can serve their purpose without the B cell going anywhere
HEV's
high endothelial venules ; circulating niave T cells can enter lymph nodes through these
2 major cellular reactions of innate immunity
inflammation and antiviral defense
mediates inflammation
cytokines
mediates antiviral defense
type 1 interferons and NK cells
role of compliment system
kill and opsonize microbes
polysaccrides and lipids stimulate secretion of these antibodies
IgM
protein antigens stimulate
T helper cells
T helper cells induce what antibodies
IgG, IgA, IgE
heavy chain class switchin
production of different antibodies all with same specificity
affinity maturation
helper T cells induce production of antibodies with higher affinity for antigen
what happens to effector lymphocytes after infectious pathogen is gone
die by apoptosis returning immune system to resting state (apoptosis)