L1&2: Innate & Adaptive Immunity Flashcards

1
Q

list examples of cell migration

A
  1. to sites of infection/inflammation
  2. from blood to lymph and vice versa
  3. from primary lymphoid organs to secondary lymphoid organs
  4. between secondary lymphoid organs
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2
Q

what is chemotaxis?

A

directional migration of cells up a concentration gradient of chemotactic molecules

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3
Q

What is IL-8 an example of?

A

a chemo/cytokine produced by macrophages which attracts neutrophils to the site of infection

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4
Q

what are chemokines?

A

chemoattractant cytokines which play a vital role in how immune cells migrate between immune organs and to sites of infection and inflammation

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5
Q

how many chemokines and how many receptors

A

47 chemokines and 19 chemokine receptors

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6
Q

what is the difference between alpha and beta chemokines?

A

the position of 2 cysteines in the protein

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7
Q

where do the cells that express CCR7 migrate to? and in response to which ligands?

A

cells expressing CCR7 will migrate to the lymph nodes in response to secretion of CCL19 and CCL21

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8
Q

What are the 3 main components of the inflammatory response?

A
  1. blood supply increases to the area affected.
  2. capillary permeability increases (allows exudation of serum proteins in surrounding tissue like Abs, complement)
  3. leukocyte migration
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9
Q

describe the sequence of events of leukocyte migration to the site of infection (hint: phased appearance)

A
  1. Neutrophils appear first (IL-8 produced by macrophages attracts them), they peak after 1-2 days, 10 fold increase in their production in the bone marrow, one way migration
  2. APCs (like macrophages, DCs) are there from the start, numbers increase, migrate to LNs to present antigens
  3. CTLs and Th cells arrive days later after their activation by APCs in the LNs & spleen
  4. B lymphocytes arrive days later, small no. as the antibodies do their work
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10
Q

can the innate system identify bacteria or viruses?

A

yes, but not very specifically, can recognize LPS

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11
Q

what is the component of the pathogen the immune system sees?

A

antigen

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12
Q

how much antibody does a health 70-80kg adult produce daily?

A

2-3g Ab (2/3 of which is IgA)

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13
Q

primary function of antbodies?

A

bind to its antigen

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14
Q

direct effector function of Ab?

A

neutralise bacterial toxins, neutralise viruses

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15
Q

secondary function of Ab?

A

activation of complement, lysis of bacteria and some viruses, opsonisation of pathogen

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16
Q

what is opsonization?

A

covering the pathogen with antibody to tag it for phagocytosis by macrophages/neutrophils, which have Fc receptors

17
Q

name general barriers or immune defences

A

skin, fatty acids, lysozyme, acid, commensal bacteria

18
Q

innate immunity response to Gram negative bacteria

A

Gram -ve bacteria are susceptible to lysis by complement

19
Q

innate immunity response to Gram +ve bacteria

A

they have a cell wall of peptidoglycan which makes them sensitive to degradation to lysozyme

20
Q

what do PRRs recognise?

A

PAMPs (pathogen associated molecular patterns)

21
Q

what happens in the proteasome?

A

proteins in the cell are degraded into short peptides and loaded onto MHC molecules, shipped out through the ER/Golgi to be presented to the outside world on the surface of the cell

22
Q

what must peptides be bound to and on where in order to be recognized by T cells

A

must be bound to MHC on either APCs or infected cells

23
Q

what do NK cells recognise?

A

the absence of MHC on the cell surface

24
Q

what do cytotoxic T cells recognise?

A

non-host peptides loaded onto MHC

25
Q

what do macrophages and other phagocytes do with the virus-infected cell they have ingested?

A

they degrade the proteins in the proteasome, load them onto MHC through the ER/Golgi apparatus and present these foreign peptides to the T cells

26
Q

what gene fusions produce the TCR

A

V, D, J, and C genes fusions

27
Q

each T cell has a unique _ which recognizes a certain _

A

each T cell has a unique TCR which recognizes a certain antigen

28
Q

what cells are MHC class I expressed on?

A

all nucleated cells

29
Q

what cells are MHC class II proteins expressed mainly?

A

mainly on antigen presenting cells

30
Q

besides foreign proteins like viral ones, what other cells’ peptides can be displayed on MHC class I

A

tumour peptides from tumour cells

31
Q

where are proteins degraded for presentation on MHC class II?

A

In endolysosomes

32
Q

perforin is produced by the _ of / and is a _ _.

A

perforin is produced by the degranulation of CTL/NK cells and is a granule protein

33
Q

what receptors do phagocytes have which facilitate phagocytosis?

A

phosphatidylserine residue receptors which bind the exposed phosphatidylserine residues on their surface

34
Q

where in phagocytes are apoptotic bodies destroyed?

A

in the phagolysosomes