6.7 Response to infection Flashcards

1
Q

what is the bodies first line of defence?

A
  • surface of body (skin)
  • lungs
  • intestine
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2
Q

what is the body’s second line of defence?

A

inflammatory response

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3
Q

define inflammation

A

rapid, localised response of our tissues to damage

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4
Q

what triggers inflammation

A

when cells are damaged, they release ‘alarm’ chemicals including histamine

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5
Q

inflammatory response

what does histamine do?

A
  • the smooth muscle of arterioles relaxes, increasing blood flow to that area.
  • cells in the walls of capillaries draw away from one another (diapedesis), so that the capillaries become ‘leaky’, forming more tissue fluid than usual. This extra tissue fluid causes local swelling of the infected area. (oedema)
  • sensory neurones become more sensitive
  • complement proteins of plasma activated
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6
Q

inflammation

what is the effect of increased blood flow + leakage of plasma

A
  • dilution and removal of toxins from invading microorganisms and from damaged cells
  • more plasma + white blood cells
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7
Q

what two leucocytes are involved inflammatory response

what do each do

A
  • neutrophils (short-lived) engulf bacteria identified by opsonins
  • macrophages engulf lather debris and damaged cells
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8
Q

what are the two main steps necessary for phagocytosis

A
  1. must distinguish foreign cells from the body’s own cells
  2. engulfs and destroys foreign cell
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9
Q

what do neutrophils and macrophages have in common?

A

both are phagocytic leucocytes

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10
Q

what are the things that help pahocytes identify foreign cells (to engulf)

and where did they come from

A

complement proteins

histamines causes them to be activated in plasma

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11
Q

3 effects of complement proteins:

A
  • attracting more phagoctyes to the site of infection
  • binding to and forming pores in the surface membrane of foreign cells, leading to lysis of these cells
  • binding to surface membranes of foreign cells thus aiding the attatchment of the surface membrane of a phagocyte to a foreign cell. These proteins are called opsinins.
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12
Q

describe phagocytosis

A
  1. phagocytic leucocyte detects presence of bacterium
  2. bacterium becomes attatched to receptor molecules on the cell surface membrane of leucocyte
  3. trapped bacterium engulfed in a food vacuole in the cytoplasm of leucocyte
  4. lysosomes in the cytoplasm fuse with the vacuole and discharge hydrolytic enzymes
  5. bacterium broken up into its constituent molecules and these are dispered into the cytoplasm (of leucocyte)
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13
Q

what are cytokines

A

a group of small proetins released by one type of cell that affects the behaviour of other cells

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14
Q

non specific still

what are interferons

what do they do

A

a group of cytokines called interferons are released by cells infected by viruses

these interferons bind to neighbouring healthy cells and trigger synthesis of antiviral proteins - as a reslut viral replication is slowed or halted.

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15
Q

what are the two types of leucocyte that are specific

A

lymphoctes:
- B lymphocytes (B cells) - humoral
- T lymphotes (T cells) - cell-mediated

bees make you laugh… humoural

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16
Q

where do both lymphocytes come from and where do they mature

A

both are produced by multipotent stem cells in marrow of some bones, t cells leave bone marrow to mature in the thymus gland whereas b cells stay in the bone marrow to mature.

17
Q

define antigen

what molecules classify

A

any molecule that can stimulate an immune response.
small molecules like amino acids and sugars do not cause an immune response
large molecules like glycoproteins, glycolipids, proteins do.
The cell surface surface of the cell is coated in antigens

18
Q

why are glycoproteins useful

A

they are highly variable and help to identify cells so are called markers

19
Q

define MHC

A

Major Histocompatability complex (MHC) protiens
Glycoproteins found on the cell surface membrane of a cell membrane of a cell that are unique to that individual. In humans, these are often called human leucocyte associated antigens (HLA).
**They help identify cells **
are types of antigen

20
Q

what do B and T cells have on their surface that allow them to recognise cells

A

antigen receptor molecules
( molecules that are complementary to very specific antigens )

21
Q

what is the consequence of the antigen-receptors on B/T cells being complementary to a specific antigen?

A

each lymphoctye can only recognise one type of antigen

22
Q

what are antibodies

A

the antigen receptor molecules of a B cell that are released.

23
Q

what are the two most common antibodies?

what are they

A

igG
igM

they are a type of protein, immunoglobin (ig)

24
Q

describe the structure of igG

A

four polypeptides linked by disulfide bridges to form a Y shape, two cghains are large (the heavy chains) and two are small (light chains)

25
Q

define self-antigen

and why do they not trigger immune response against themselves

A

a glycoprotein on the cell surface membrane of one of the body’s own cells.
(The ability of this glycoprotein to cause an immune response is reduced by the body destroying any randomly produced lymphocytes with a complementary antigen-receptor. )

26
Q

what is the humoral response

A

response involving the release of antibodies by B-cells.

27
Q

outline the humoral response

A
  1. antigen to antibody on the B cell surface membrane
  2. antigen taken up by exocytosis and is expressed on the cell surface membrane at the MHC protien
  3. Meanwhile.. macrophages engulf antigens by endocytosis and then express this antigen on their MHC proteins on the cell surface membrane = antigen presentation
  4. T cell binds (briefly) to macrophage that presents an antigen and is activated- it is now an activated T helper cell
  5. activated T helper cell now binds to B cell with the same antigen expressed-immediately the B cell is activated = activated B cell
  6. activated B divides rapidly forming a clone of plasma cells - each containg lots of rER now mass producing antibody molcules that are secreted by exocytosis
  7. (some activated B cells and T cells surviuve in the body as memory cells, and are able to initiate a more speedy response in the event of re-infections
    antibodies overcome antigen eg by neutralising it by causing clumping together of cells to aid engulfing by other macrophages
28
Q

outline the cell mediated response

A
  1. complementary T cell binds to macrophae presenting complementary antigen = activated T helper cell
  2. T helper cells release cytokines that stimulate T helper cell to divide repeatedly to form clones
    clone could be three types of T helper cell
29
Q

3 types of T cell (from clone)

A
  • T killer cells- destroy body cells infected by virus or other cells carrying for example TAA (tumor associated antigens)
  • T helper cells- release cytokines that stimulate the production of B cells
  • Memory cells- remain in the body and bring about the secondary response (re-infection).
30
Q

contrast primary and secondary immune reponse (re-infection)

A

secondary is
- faster rate of antibody production
- shorter time lag between exposure an antibody production
- higher concentration of antibodies
- antibdoy level remains higher after the secondary response
- pathogen usually destroyed before any symptoms

31
Q

similarities between passive and active immunity

A
  • both involve antibodies
  • both can be natural or arificial
32
Q

give examples of passive and active immunity

A

passive natural: antibodies in breast milk
passive artificial: anti-venom
active natural: humoral response to infection
active artificial: vaccination

33
Q

contrast passive and active immunity

A

passive:
- no memory cells and antibodies not replaced when broken down= short term
- immediate
- antibodies from external source
- direct contact with antigen not necessary

active:
- memory cells produced = long-term memory
- time lag
- lymphocytes produce antibodies
- direct contact with the antigen necessary

34
Q

explain the principles of vaccination

A
  1. vaccine contains dead/inactive form of a pathogen or antigen
  2. triggers primary immune reponse
  3. memory cells are produced and remian in the bloodstream so secondary response is rapid and produce higher conc of antibodies
  4. pathogen is destroyed before it causes symptoms.
35
Q

what is herd immunity?

A

vaccinating 80-90% of population reduces available carriers of the pathogen to control disease transmission

protects individuls who have not been vaccinated eg: those with a weak immune system.