Antibacterial Mechanisms Flashcards

1
Q

What is an example of a biochemical mechanism used as defence against pathogens?

A

Sebaceous gland secretions - fatty acids, enzymes, antibacterial defences

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2
Q

What is the difference between commensal and pathogenic microbes?

A

Commensal: good bacteria

Pathogenic: bad bacteria

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3
Q

What is the purpose of the lymphatic drainage?

A

It drains white blood cells & carries them around the body.

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4
Q

What is the purpose of post-capillary venules?

A

They can open to allow plasma proteins/leukocytes to escape from the blood.

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5
Q

What 4 things are associated with acute inflammation?

A
  1. Tumor: swelling
  2. Calor: heat
    3: Rubor: redness
    4: Dalor: pain
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6
Q

What is the complement system?

A

Complement is a protein made in the liver, which can be activated by pathogens/antibodies.
It enhances the ability of phagocytes/microbes to clear pathogens.

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7
Q

What on the microbes cell surface activates the complement system, and what process occurs after?

A

PAMPS (pathogen associated molecular patterns) activate the system, and phagocytosis takes place.

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8
Q

What do component parts of the complement system break down into?

A

They break down into bits of complement.

E.G. complement 1 can be broken down into 2, 3, 4, 5, etc

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9
Q

Which 2 complement proteins are involved in inflammation?

A

C3a & C5a.

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10
Q

What is C3b responsible for?

A

Opsonisation of phagocytosis, which sticks to the pathogen & engulfs it.

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11
Q

What are the 3 possible effects of complement activation?

A
  1. Opsonisation & phagocytosis
    - C3b or C4b bind to microbe
    - Phagocyte with a C3b receptor recognises this
    - Phagocytosis of microbe occurs
  2. Stimulation of inflammatory reactions
    - C3b binds to microbe, C3a & C5a is released
    - These recruit & activate leukocytes
    - Destruction of microbe via leukocytes occurs
  3. Complement-mediated cytolysis
    - C3b binds to microbe & activates late components of complement
    - Formation of MAC (attack complex) occurs
    - Osmotic lysis of bacteria occurs
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12
Q

What are C3a, C4a & C5a collectively known as?

A

Anaphylatoxins.

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13
Q

Which 2 complement fragments act on mast cells to release histamines?

A

C3a and C5a.

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14
Q

What causes the redness and heat during inflammation?

A

Vasodilation, which also increases the vol. of WBCs to the area.

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15
Q

What causes swelling in inflammation?

A

Blood vessels become leaky with water, which causes the swelling.

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16
Q

What 2 things does C3a, C4a and C5a induce?

A
  1. Acute inflammation

2. Chemotaxis (movement of cells in response to a stimuli)

17
Q

Which pro-inflammatory cytokines can induce the production of complement, and which type of cell releases them?

A

Macrophages can release TNF-alpha and IL-1 to send to the brain & cause a fever.

18
Q

Which pro-inflammatory cytokine can be activated/released by NK cells?

A

IFN-gamma

19
Q

When are lymphocytes activated?

A

When the innate response is not enough to fight the pathogen.

20
Q

What is the process in which the adaptive immune response is activated?

A
  1. Dendritic cells mature & increase their antigen presenting capability
  2. Dendritic cells & immature T helper cells meet in the lymph nodes
  3. Toll-like receptors binding to phagocytes activate more cytokines
  4. Macrophages can also act like APC’s localised at the site of the infection
  5. Adaptive immune response is then activated
21
Q

What do MHC molecules do?

A

They display antigens, which are required for a full T cell response.

22
Q

Where are naive T cells generated?

A

In the thymus, where they have not interacted with an APC yet.

23
Q

Where do naive T cells reside?

A

In the lymph nodes.

24
Q

What can activation of T cells stimulate?

A
  1. Stimulation of B cells (producing antibodies)
  2. Cytotoxic T cells
  3. Cytokines
  4. Effector T cells
25
Q

What do B cells turn into?

A

They turn into plasma cells which are bigger & produce antibodies.