Unit 6- Response To Infection Flashcards

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1
Q

What cells are responsible for phagocytosis? 3

A

Phagocytes: neutrophils, monocytes and macrophages

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2
Q

How have phagocytes adapted?

A

Complex cytoskeleton that allows them to change shape
Contain lysozymes
Large

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3
Q

Describe phagocytosis:

A
  • phagocytes move through blood/tissue fluid in response to chemicals
  • they surround and engulf the foreign body (phagocytosis)
  • microbes are trapped in phagosome which fuses with lysosome
  • the lysozymes hydrolyse the microbe proteins, carbs and fats
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4
Q

Where do the different phagocytes work?

A

Neutrophils -blood

Macrophages and monocytes - tissue fluid/lungs and other spaces

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5
Q

What causes inflammation?

A

Granulocytes release chemicals (prostaglandins and histamines) which stimulates inflammation

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6
Q

What changes occur in inflammation? Name 4

A
  • vasodilation
  • capillary leakage (so phagocytes and granulocytes can enter)
  • sensory neurone impulses (tender areas)
  • blood clotting
  • fever (the heat kills more pathogens than human cells)
  • tissue repair (collagen deposits and stimulation of new cell growth makes scar tissue)
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7
Q

What make up the non-specific immune response?

A

Phagocytosis and inflammation

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8
Q

What cells make up the specific immune response?

A

B-lymphocytes and T-lymphocytes

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9
Q

How do we know the specific immune response is a later evolutionary advancement?

A

Only vertebrates have it as the cells that are involved are made in the bone marrow

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10
Q

What are antigens?

Clue: antigen is short for (ANTIbody GENerators)

A

Large molecules that bind to lymphocytes triggering a specific immune response

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11
Q

Which cell makes antibodies?

A

B-lymphocytes

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12
Q

What is an antibody?

A

A protein molecule that can bind specifically to an antigen

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13
Q

Structure of an immunoglobulin:

A

4 polypeptide chains (2 heavy and 2 light chains)
Joined by disulphide bonds to form a Y shape
They all have the same constant region (stem) and different variable regions (different amino acid sequences)
Which leads to a highly specific antigen-antibody complex

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14
Q

What is self recognition?

A

When cells are able to recognise the cell is not foreign by the distinct marker proteins (MHCs) on the cell membrane

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15
Q

What are receptors and where are they found?

A

They are proteins witch only 1 binding site (unlike antibodies 2) found on surface of T-lymphocytes

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16
Q

What do receptors do?

A

They bind to specific antigens forming an antigen-receptor complex

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17
Q

What is the main antigen presenting cell?

A

Macrophage phagocytes as they are in largest abundance

18
Q

What is the macrophages role in the first step of infection from antigens?

A

In order to initiate the specific immune response a macrophage needs to engulf the pathogen and present the antigen on its surface becoming an antigen-present cell

19
Q

What are cytokines and what cell releases them?

A

They are chemicals which stimulate clonal selection, released from macrophages and T-helper cells

20
Q

Describe clonal selection from antigen presenting cell:

A

Eventually a helper T cell with a complementary receptor to the antigen will bind to antigen
The T helper cell releases cytokines which stimulate immature T and B lymphocytes to activate, proliferate and differentiate
The activated cells divide by mitosis making a clone army of cells with identical binding sites that is specific to the foreign antigen

21
Q

How do T killer cells kill the infected cells?

A
  • bind to antigens on infected cells
  • secrete porin proteins
  • porin makes pores in the cell membrane so water diffuses in
  • the infected cell bursts (lysis)
22
Q

What cells are part of cellular immunity?

A

Cytotoxic/killer T cells and memory T cells

23
Q

Which cells are part of the humoral immunity?

A

B-lymphocytes which differentiate into thousands of plasma cells
Memory B cells

24
Q

What is the job of plasma cells?

A

To synthesise antibodies specific to the antigens

25
Q

Why is it called humoral immunity?

A

Because antibodies are being secreted into the blood plasma (humour)

26
Q

How do antigens prevent infection?

A
  • agglutination
  • opsonisation (marking a pathogen for phagocytosis)
  • binding to antigens on virus’ or bacteria prevents them attaching to host cells (blocks antigens)
  • precipitation, binding to free soluble toxin proteins (blocking/changing their shape) making them insoluble
  • lysis
27
Q

Why do some of the activated B and T cells divide into memory cells?

A

Memory cells remain in the blood for years

  • if the same antigen is encountered again memory cells divide quickly into plasma cells and killer cells
  • this skips clonal selection
  • secondary immune response
28
Q

What is antigenic variability?

A

When pathogens develop new strains with different antigens

  • due to mutation
  • we cannot become immune
29
Q

What is vaccination?

A
  • injecting a person with a modified non-virulent strain to promote a primary immune response and make memory cells to that specific antigen
  • when the real strain invades the secondary immune response will be able to recognise and kill it quickly
30
Q

What is active immunity?

A

Any process that promotes a primary immune response leaving memory cells
Eg. Vaccination or catching a disease

31
Q

What is passive immunity?

A

When antibodies are received

Eg. Breastmilk or across the placenta

32
Q

When does passive immunity happen naturally?

A

When antibodies are passed across the placenta to the baby

In breast milk

33
Q

When does passive passive immunity happen artificially?

A

Achieved through injection of antibodies in an antiserum

Eg. To combat AIDS

34
Q

Why could some people not receive vaccines?

A
  • newborns with weak immune systems
  • people with immunosuppressant diseases
  • those undergoing chemotherapy
35
Q

What is herd immunity?

A

When the majority of a population (85-95%) are vaccinated, so there are not enough hosts for the disease to survive and reproduce

36
Q

What are free riders?

A

People who choose not to get vaccinated compromising the threshold for herd immunity

37
Q

What are T suppressor cells?

A

Cells that stop the response when an antigen has been removed, so the response doesn’t get too over the top and you begin wasting resources

38
Q

Purpose of T helper cell?

A

To stimulate a specific immune response

39
Q

Explain how the non specific immune response protects against infection by bacteria

A
  • bacteria don’t have MHCs so are recognised as foreign
  • phagocytes engulf the bacteria
  • neutrophils engulf and digest bacteria
  • monocytes become macrophages which also ingest and digest bacteria
  • they release cytokines to attract other phagocytes to site of infection, increasing blood flow and inflammation
40
Q

Describe the interaction of immune cells in producing a hormonal response

A
  • macrophages present antigen to activate T helper cells

- T helper cells activate B cells by recognising antigen and producing cytokines

41
Q

Similarities of humoral and cell mediated response

A
  • both are specific to an antigen
  • both require the formation of APCs and the presence of MHCs
  • both involve clonal selection which is activation of only those cells which recognise the antigen
  • both involve differentiation of cells, following activation by T helper cell