wk 6- innate immunity Flashcards

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1
Q

difference between primary and secondary lymphoid organs/tissues

A

Primary lymphoid organs are the site of lymphocyte maturation and
secondary lymphoid organs and tissues are the sites of pathogen encounters.

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2
Q

what are muscosa-associated lymphatic tissue

A

nodal patches of lympathic tissue in the mucosal linings

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3
Q

where do B-lymphocytes and T-lymphocytes mature?

A

primary lymphoid organs that mature in
B- red bone marrow of long bones
T- thymus

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4
Q

changes in thymus during adulthood, what happens

A

it is large in early life but atrophies in adulthood and is replaced by fatty connective tissue

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5
Q

difference between afferent lymphatic vessels and efferent?

A

a- the point of unfiltered lymph into the lymph node
e- the point of exit of filtered lymph out of the lymph node

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6
Q

what is mucosa-associated lymphatic tissue?

A

nodal patches of lymphatic tissue in the mucosal linings

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7
Q

what 2 responses is the immune system made up of? and what do they do?

A

innate immune response and adaptive immune response. They work together to recognize, target and remove infectious agents from the body. The innate response is more rapid and less specific than the adaptive immune response

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8
Q

characteristics of innate immune response 4

A

non specific response (one size fits all)
rapid response (minutes to hours)
no memory
present at birth

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9
Q

characteristics of adaptive immune response 4

A

specific response (targeted)
slow response (lag time, delays)
immunological memory
antibodies
develops over time

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10
Q

components of innate immune response 3

A

physical/mechanical factors:(skin/mucous membranes)
cellular factors: (phagocytic cells, antigen presenting cells)
soluble factors (enzymes, pyrogens (fever) , complement)

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11
Q

list and describe phagocytic cells

A

cell eaters

monocytes
macrophages
neutrophils
dendritic cells

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12
Q

myeloid progenitor cells include what cell types

A

red blood cells, granulocytes (dendritic),monocytes and platelets

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13
Q

lymphoid progenitor cells include what cell types

A

lymphocytes and NK cells

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14
Q

myeloid cells are apart of what immune respnse

A

innate

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15
Q

lymphoi are apart of what immune response

A

adaptive

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16
Q

components of adaptive immune responses 2

A

cellular factors (lymphocytes, NK cells)
soluble factors (antibodies, enzymes)

17
Q

where do immune cells come from?

A

immune cells are derived from red bone marrow in a process called haemoatpoiesis.
from here they transition from stem cells to progenitor cells and finally mature cells via two lineages.

the myeloid progenitor cells produce the innate immune response cells and the lymphoid progenitor cells produce the adaptive immune response cells.

18
Q

most common cell in the innate immunity to respond

A

neutrophils

19
Q

an effective Immune system must be able to: 6

A
  1. remain inactivated/switched-off under normal physiological conditions
  2. be activated by infectious agents (recognition of pathogens)
  3. produce a tailored response to specific pathogen groups (extracellular versus intracellular)
  4. respond at the site of infection (recruitment of immune cells)
  5. be regulated (turned off when pathogen is cleared)
  6. prevent/minimise damage to self-tissues
20
Q

chemotaxis is?

A

used to describe the recruitment/movement of immune cells towards a chemical stimulus (site of infection or trauma)

21
Q

soluble facts for innate immune responses

A

complement system - soluble complement proteins which initiate opsonisation: coat infectious agents for easy phagocytosis, membrane attack complex: causing cell lysis,
causes inflammation: reducing reproduction of agent
chemotaxis: recruitment of phagocytosis

also
sweat, oil, digestive enzymes, mucous, etc

22
Q

what does phagocytosis do? what do they target, what is the process?

A

target EXTRACELLULAR pathogens
Phagocytosis is triggered by pattern recognition. Phagocytic cells enclose infected cells in vesicles, to which enzymes from lysosomes are added, resulting in destruction of the pathogen. Phagocytosis is effective for targeting extracellular pathogens such as bacteria, protozoa and fungi.

23
Q

what do natural killer cells and interferon (NK and IFN) do?

A

target intracellular pathogens

Production of interferon interferes with viral replication via:
1. inhibition of viral protein synthesis
2. degradation of viral nucleic acids
3. inhibition of viral gene expression and virion assembly

(viruses are intracellular pathogens)

24
Q

what cells target intracellular and extracellular pathogens?

A

intra- NK and IFN
extra- phagocytic cells

25
Q

what is an early innate response to exposure of an infectious agent?

A

fever

Reproduction of microbial cells is optimal at core body temperature, if the temperature is increased by one to two degrees Celsius, then the replication rate of microbial cells is significantly impaired. A reduction in the replication rate of the pathogen allows time for the host immune cells to be recruited to the site of infection. Pyrogens are chemical mediators of hypothalamic temperature control and a reproduced by phagocytic cells.

26
Q

steps of acute inflammation 8

A
  1. disruption to barrier integrity (trauma/infection)
  2. epithelial cell activation pattern recognition receptor signaling: production of host antimicrobial peptides
  3. activation of complement pathway: opsonisation, inflammation, killing
  4. activation of resident phagocytes: phagocytosis and cytokine production
  5. cytokines and complement activate local vascular endothelium: increased cell recruitment and vascular leakage
  6. increased phagocytosis, complement and HDP activity
  7. resolution of infection
  8. activation of adaptive immunity
27
Q

what is complement and what does the activation result in / steps ?

A

Activation of complement results in a cascade of proteolytic cleavage of large proteins to facilitate the effects of antibody. Without the production of complement, antibody cannot destroy invading pathogens.

steps:
1. inflammation
2. opsonisation to coat the infectious agent for easy capture by phagocytic cells (C3b)
3. phagocytosis (C5a) via chemotaxis results in recruitment of phagocytic cells to the site of infection
4. cell lysis caused by pore formation caused by membrane attack complex (MAC)

28
Q

initiation of complement activation can happen how? 3

A

complement activation (C3) can be activated via three pathways:
(1) the lectin pathway,
(2) the classical pathway, and
(3) the alternative pathway.

29
Q

examples of mechanical factors 5

A

intact skin
mucous production
ciliated epithelium
low pH
acid production

30
Q

examples of soluble factors 4

A

pyrogens (fever)
lysozymes
interferon
complement

31
Q

examples of cellular factors

A

neutrophils
macrophages
dendritic cells
monocytes
phagocytic cells

32
Q

what turns on innate immunity?

A

pattern recognition through toll-like receptors, responsible for recognizing molecules that are highly conserved across classes of pathogens

can be intracellular to recognize viruses or extracellular.

33
Q

what are antigen presenting cells

A

present infection to the adaptive immune system