abbas chapter 1 Flashcards

1
Q

innate immunity

A
always present
blocks entry of microbes
includes:
- epithelial barriers
- phagocytes (esp. NK cells)
- complement

takes 6-12 hours
doesn’t react against noninfectious foriegn sugstances

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2
Q

adaptive immunity

A

B-lymphocytes create antibodies
T-lymphocytes become effector T cells
acts 1-5 days post infection
recognizes antigens but only recognized if the antigens are delivered to lymphatics

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3
Q

types of adaptive immunity

A

humoral and cell-mediated

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4
Q

humoral immunity

A

for extracellular microbes
antibodies produced by B lymphocytes
B lymphocytes recognize extracellular antigens

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5
Q

cell-mediated immunity

A

for intracellular microbes
t-lymphocytes activate phagocytes and kill host cells
t lymphocytes recognize antigens produced by intracellular microbes

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6
Q

humoral immune response (microbe type, responding lymphocytes, effector mechanism, functions)

A
  • extracellular microbe
  • B lymphocytes respond
  • secrete antibody
  • block infections and eliminate extracellular microbes
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7
Q

cell-mediated response (microbe type, responding lymphocytes, functions)

A

if phagocytised microbe:

  • microbe in macrophages
  • helper T lymphocytes respond
  • activate macrophages to kill phagocytosed microbes

if intracellular microbes:

  • intracellular microbes replicate within the infected cells
  • cytolytic T lymphocytes respond
  • kills infected cells and eliminates reservoirs of infection
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8
Q

clonal selection hypothesis

A

mature lymphocytes with receptors for many antigens develop before the encounter with those antiges - when antigen presents, that clone cell proliferates

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9
Q

primary immune response

A

response to first exposure to antigen

mediated by naive lymphocytes

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10
Q

secondary immune response

A

due to subsequent encounters with same antigen that created a primary immune response
faster and larger response due to activation of memory lymphocytes

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11
Q

phases of response (list)

A

recognition
activation of lymphocytes
- clonal expansion
effector phase

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12
Q

recognition phase

A

first phase of immune response

naive antigen-specific lymphocytes locate and recognize the antigens of microbes

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13
Q

activation phase

A

second phase of immune response
requires binding of antigen to antigen receptors of lymphocytes (signal 1) and other signals from microbes and innate immune system (signal 2)
includes clonal expansion step
some lymphocytes also differentiate into effector cells - secrete antibody (b) or kill infected cells (t)

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14
Q

clonal expansion

A

occurs during activation phase of immune response

rapid cell division of lymphocytes that encounter antigens

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15
Q

effector cells

A

generated during clonal expansion step of immune response
some B cells secrete antibody and some T cells kill infected cells
include lymphocytes and other leukocytes - B and T leukocyte lineages, and also granulocytes and macrophages

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16
Q

effector phase

A

third phase of immune response
effector cells and their products eliminate
only become effector cells when naive lymphocytes get both 1st and 2nd signals

17
Q

what happens to cells from the immune response after the infection is eliminated?

A

most cells that were activated die via apoptosis

memory lymphocytes remain and migrate through lymph - some go to site of infection

18
Q

lymphocytes

A

the only cells with specific receptors for antigen
key mediators of adaptive immunity
B - mediate humoral response - produce antibodies
T - mediate cell-mediated immunity - only recognize antigens bound to mHC on APCs
NK cells - innate immunity
CD4+ cells and CD8+ cells

19
Q

CD4+ cells

A

mature in bone marrow
helper T cells because help B to produce antibodies and help phagocytes to destroy ingested microbes
reduce cytokines
when become effector cells, produce cytokines that activate B cells and macrophages

20
Q

CD8+ cells

A

cytolytic or cytotoxic = CTLs
kill cells harboring intracellular microbes
mature in thymus

21
Q

B cells

A

mediate humoral immunity
produce antibodies
b-cells become effector cells - become plasma cells - secrete antibody

22
Q

antigen presenting cells

A

in epi
capture antiges and transport them to peripheral lymphatic tissue
includes dendritic cells, macrophages

23
Q

dendritic cells

A

professional APCs
capture protein antigens of microbes tht enter through epithelia and transport antigens to lymph nodes where portions of antigen recognized by T lymph

24
Q

macrophages

A

in epithelium, phagocytose microbes that invade

display these protein antigens to T cells

25
professional APCs
also present secondary signals to help activate T cell proliferation and differentiation
26
generative tissues of immune system
primary | T and B lymphocytes mature and become competent to respond here
27
peripheral tissues of immune system
secondary where adaptive immune responses to microbes instigated lymph nodes, spleen, mucosal and cutaneous immune systems concentrate antigens, APCs and lymphocytes T and B separated into different anatomical compartments - kept there by cytokines expressed in those areas
28
lymph nodes
peripheral/secondary tissue substances absorbed from epithelia and tissues APCs in nodes sample antigens in lymph as it passes through nodes and dendritic cells go here antigens become concentrated in draining lymph nodes B cells are in follicles in the cortex (FDCS there too), while T outside follicles (as are dendritic cells) follicles have germinal center when activated
29
spleen
blood equivalent to the lymph node dendritic cells and macrophages trap and concentrate blood borne antigens - lots of phagocytes B in follicles too
30
cutaneous and mucosal immune tissues
cutaneous under epithelium | mucosal in GI and respiratory tracts (peyers patches and pharyngeal tonsils)
31
T lymph maturation
matures in thymus migrate to lymph nodes through HEVs activated by macrophages or other APCs presenting antigens they then differentiate and proliferate and migrate into tissues colonized by infectious microbes
32
high endothelial venules (HEVs)
mature t lymphocytes migrate into lymph nodes through them express carbohydrate ligands that bind to L-selectin receptor on naive T cells so that the naive T cells bind losely to HEVs cytokines expressed in paracortical regions induce t cells to bind more finally to HEVs and migrate through