Innate Immunity Flashcards

1
Q

What are the three phases of response to initial infection? when do they occur?

A

Innate Immunity; this occurs immediately (0-4hrs) as components are already formed.
Early induced response; Early (4-96hrs) involves the recruitment of cells
Adaptive immune response (96+hrs) involves making new immune cells and antibodies

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2
Q

What are some mucosal surfaces where pathogens can enter?

A

Airway, GI tract and Gu

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3
Q

Name a pathogen that enters via the airway and what disease it causes?

A

Influenza Virus causing influenza

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4
Q

Name a pathogen that enters the GI tract and what disease it causes?

A

Salmonella causing typhoid fever

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5
Q

Name a pathogen that enters through the GU and what disease it causes?

A

Treponoma Pallidum causing syphilis

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6
Q

Name the ways in which pathogens can enter through external epithelia

A

External surface, wounds and abrasions, and insects bites

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7
Q

Name a pathogen that enters through external surface of epithelium and the disease it causes?

A

Tinea Pedis causing Athlete’s foot

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8
Q

Name a pathogen that enters through wounds and abrasions and the disease it causes

A

Clostridium tetani causing tetanus

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9
Q

Name a pathogen that enters via inset bites and the disease it causes

A

Plasmodium causing malaria

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10
Q

What are the different barriers to infection and name some specific examples

A

Mechanical - movement of cilia and tight junctions between cells
Chemical - Fatty acids on skin & Stomach acid.
Microbiological - Normal flora to compete for nutrients and attachment

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11
Q

One pathogen crosses epithelial barrier what occurs? And what is this enhanced by?

A

It is recognised and ingested by mono-nuclear phagocytes or macrophages. This is enhanced by the presence of receptor on the phagocytic cell that can recognise pathogens

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12
Q

Name some of the bacericidal effects and agents produced by phagocytes

A
  • Acidification (acidic environment)
  • Toxic oxygen derived products
  • Toxic nitrogen oxides
  • Peptides (defensins)
  • Enzymes (lysosmye)
  • Competitors (lactoferrin)
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13
Q

All cells of the immune system are derived from what?

A

Haemotopoeitic stem cell

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14
Q

What is key about the circulation time of neutrophils

A

They only circulate for 12 hours. So if a drug or agent is affecting the immune system this is first seen here.

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15
Q

What do mast cells release?

A

Substances that effect vascular substances. They are full of histamine

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16
Q

What is the function of B and T cells

A

B cells - Production of antibodies

T cells - Become cytotoxic T cells (CD8) or helper T cells (CD4)

17
Q

What are neutrophils, basophils and eosinophils involved in?

A

Neutrophil - Ingest bacteria
Eosinophil - Important in parasite defence
Basophils - Involved in hypersensitivity reactions

18
Q

What is the role of natural killer cells and dendritic cells?

A

Natural Killer - Recognise virally infected cells

Dendritic cells - Bridges innate and adaptive immune responses (antigen presenting cells)

19
Q

What do virally infected cells release?

A

Interferon alpha (IFN-α) and Interferon Beta (IFN-β)

20
Q

What does the release of IFN-β and IFN-α cause?

A

Near by cells to become slightly more resistant to the virus, upregulates a class of proteins called MHC class 1 and finally activates other natural killer cells.

21
Q

Describe what Natural Killers cells interact with and what happens when the cell is infected?

A

They interact with MHC class 1 receptors on healthy cells and this stops the NK from killing it. However when a cell is infected with a virus it no longer produced MHC class 1 receptors so the NK cannot interact and therefore it kills the cell

22
Q

What are two of the main complement pathways and what activates them?

A

Classical Pathway - Antibody binds to specific antigen on pathogen surface
Alternative Pathway - Pathogen surface creates local environment which triggers complement activation

23
Q

What are some of the outcomes for the complement system?

A
  • Recruitment of cells
  • Opsonization of pathogens
  • Lysis and death of pathogens
24
Q

Name an example of an opsonin

A

C3b

25
Q

Name two examples of mediators of inflammation

A

C5a and C3a

26
Q

What is the classical pathway initiated by?

A

Activation of the c1 complex which binds to antigens on the pathogen surface.

27
Q

What occurs tp C3 in the complement cascade?

A

It is cleaved into C3b which sticks to the cell acting as an opsonin and C3a floats away and recruits more cells.

28
Q

What is the alternative pathway caused by?

A

The spontaneous hydrolysis of serum C3. C3b then binds to pathogen surface creating that environment which triggers the alternative pathway.

29
Q

What forms the membrane attack complex (MAC) and what does it do

A

It is formed from complement serum proteins; C6, C7, C8, and C9 and it punches wholes in the surface of pathogens causing it to die

30
Q

What is the function of CD59?

A

It prevents membrane attack complexes from forming on the surface of host cells. SO it is there for protection

31
Q

Name some examples that inhibit the complement system and why this is needed

A

DAF, MCP and Cr1. This is to prevent immune responses when they are not needed.

32
Q

Patients with complement Deficiencies often present with what?

A

Recurring bacterial infections which differ depending on which complement serum protein they are deficient in.