Topic 1 Flashcards

1
Q

Innate Immune cells recognise…

A

danger signals

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2
Q

Examples of danger signals which innate immune cells detect

A

PAMP’s (Pathogen Associated Molecular Patterns) and DAMP’s (Damage Associated Molecular Patterns)

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3
Q

What is meant by the complement system?

A

A collection of proteins which work together as an early warning system to fight pathogens. Some lyse pathogens, others label microbes for phagocytes to detect, and others recruit other immune cells

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4
Q

How is the complement system activated?

A

There are 3 potential pathways. The alternative pathway, the lectin pathway or the classical pathway.

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5
Q

How does alternative pathway work?

A

Complement proteins such as c3b are spontaneously produced. What these do is they bind to the amino and hydroxyl groups of microbes which cause the complement effector mechanisms to activate

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6
Q

How does the lectin pathway work?

A

Well, mannose is a common surface carbohydrate which is found on the surface of many pathogens. Because of this, Mannose binding Lectin binds to the mannose.

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7
Q

Mannose is an example of a

A

Pathogen Associated molecular pattern (PAMP)

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8
Q

Mannose binding lectin is an example of

A

A Pattern recognition receptor (PRR)

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9
Q

Sentinel cells include…

A

Macrophages and Dendritic Cells

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10
Q

Properties of Macrophages include

A
  1. they dont move from infection site
  2. talk to T cells at infection site
  3. Good killer
  4. Good all rounder
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11
Q

Properties of Dendritic cells include

A
  1. Migrate from site of infection to LN (lymph node)
  2. Talk to T cells in LN and infection site
  3. Doesnt kill
  4. Specialised in talking with T cells
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12
Q

Macrophages as sentinels….

A

They are found in all barrier tissue, they mop up apoptotic cells, remove debris and scan the environment

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13
Q

First danger signal comes from

A

DAMP’s

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14
Q

The first danger signal causes

A

Cytokines to be released and complement pathway to activate. Macrophages are ready for action

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15
Q

The second danger signal comes from

A

PAMP’s

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16
Q

Examples of second danger signals are

A

cell wall glucans (bacteria), double stranded RNA (viruses), lipopolysaccharide (lps)

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17
Q

PRR’s can be

A

Intracellular and Extracellular

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18
Q

During inflammation, cytokines…

A

are released (TNF-alpha is a good example)

19
Q

Neutrophils

A

are recruited from blood to infection site. They conduct phagocytosis of pathogens.

20
Q

When natural killer cells are called, they release

A

cytokines such as TNF-y which activates macrophages

21
Q

What condition arises when PAMP’s act as toxins

A

sepsis (which can ultimately lead to septic shock)

22
Q

T and B cells recognise

A

Antigens (Ag)

23
Q

An epitope is…

A

The precise part of the antigen which is recognised by the T or B cell receptor

24
Q

A paratope is…

A

The part of an antibody or T cell receptor that binds an epitope.

25
Q

Regulatory T cells

A

Suppress the immune response at appropriate times

26
Q

Cytotoxic T cells

A

kill infected cells

27
Q

Helper T cells…

A
  1. Activate macrophages
  2. Cause the activation of the immune response.
  3. Activate further T and B lymphocytes
28
Q

B lymphocyte cells…

A
  1. Neutralize microbes
  2. Phagocytosis
  3. Complement activation
29
Q

How do T cells recognise antigens?

A

via Antigen presenting cells only

30
Q

How do B cells recognise antigens?

A

On their own without any prerequisite

31
Q

T cells recognise antigens…

A

using T cell receptors which bind to antigen presenting cells

32
Q

B cells recognise receptors by

A

Either having a surface Immunoglobulin bind and interact with an antigen or secrete an antibody which can bind to the antigen

33
Q

A T cell antigen must be

A

a protein (which is then later broken down into peptides)

34
Q

A B cell antigen can be

A

Anything organic (and can bind in a linear fashion or discontinuous)

35
Q

T cell receptor consists of…

A

2 chains (alpha and beta) (although T cell receptors have 1 binding site)

36
Q

B cell receptor consists of

A

2 heavy chains and 2 light chains (and has 2 binding sites)

37
Q

Antigen receptors are created via…

A

somatic recombination

38
Q

Junctional diversity occurs by

A
  1. Having non-precise v,d, and j joinings
  2. addition of bases
  3. deletion of bases
  4. sequence alignment
  5. filling in the gaps
39
Q

what is clonal expansion?

A

where T/B cells see their Antigens and become active, the time required to activate and expand Ag specific T/B cells is slow, which explains why adaptive immunity is slow

40
Q

How does Immune evasion occur?

A

Antigenic variation

41
Q

T and B cells cannot…

A

tell what they are recognising

42
Q

Central Tolerance is…

A

a mechanism by which T and B cells which recognise self antigens are removed/ destroyed.

43
Q

Self reactive T cells are removed in

A

the thymus

44
Q

Self reactive B cells are removed in

A

the bone marrow