Inflammation Flashcards

L3 (46 cards)

1
Q

What is inflammation?

A

An innate immune response to infection or tissue damage that eliminates pathogens, removes damaged tissue, and initiates repair

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Which arm of the immune system does inflammation belong too?

A

Innate immunity

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What triggers an inflammatory response?

A

Infection, tissue injury, or recognition of pathogens by innate immune cells

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What are the main goals of inflammation?

A

Pathogen elimination, containment of infection, and initiation of tissue repair

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are the 4 classical signs of inflammation?

A
  1. Calor (heat)
  2. Dolor (pain)
  3. Rubor (redness)
  4. Tumor (swelling)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What causes redness and heat during inflammation?

A

Increased blood flow due to vasodilation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What causes swelling during inflammation?

A

Increased vascular permeability allowing fluid to enter tissues.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What causes pain during inflammation?

A

Pressure from swelling and sensitisation of nerve endings by inflammatory mediators

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What are cytokines?

A

Small signalling proteins released by immune cells that regulate immune and inflammatory responses

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Which cytokines act as endogenous pyrogens?

A

TNF-α, IL-1 (and IL-6)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

How do cytokines cause fever?

A

They induce prostaglandin E2 production in the hypothalamus, raising body temperature.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Why is fever beneficial during infection?

A

It inhibits bacterial growth and enhances adaptive immune responses

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

How does the body conserve heat during fever?

A

Vasoconstriction reduces heat loss

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Which cells usually initiate inflammation in tissues?

A

Macrophages (and dendritic cells)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

How do macrophages recognise pathogens?

A

Through pattern recognition receptors (PRRs)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What happens when macrophages recognise a pathogen?

A

They release cytokines and chemokines that initiate inflammation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
17
Q

What is chemotaxis?

A

Directed movement of immune cells toward increasing concentrations of chemokines

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
18
Q

Which immune cells are recruited first to sites of inflammation?

A

Neutrophils

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
19
Q

What is extravasation?

A

The movement of leukocytes from the bloodstream into infected tissues

20
Q

What is phagocytosis?

A

The engulfment and intracellular destruction of pathogens by phagocytes

21
Q

List the key steps of phagocytosis?

A
  1. Recognition
  2. Engulfment (phagosome formation)
  3. Phagolysosome formation
  4. Killing and digestion
  5. Antigen presentation
22
Q

What is a phagolysosome?

A

A vesicle formed by fusion of a phagosome with a lysosome, where pathogens are destroyed

23
Q

What happens to antigenic peptides after phagocytosis?

A

They are loaded onto MHC class II molecules

24
Q

What is antigen presentation?

A

Display of processed antigenic peptides on MHC molecules for recognition by T cells

25
Which MHC class presents antigen from phagocytosed pathogens?
MHC class II
26
Which T cells recognise MHC class- II presented antigen?
CD4⁺ helper T cells
27
Name the 3 main antigen presenting cells (APCs)?
1. Dendritic cells 2. Macrophages 3. B cells
28
What are PRRs?
Germline-encoded receptors that recognise pathogen-associated molecular patterns (PAMPs)
29
What are PAMPs?
Conserved molecular structures found on pathogens but not host cells
30
Why are PRRs important for innate immunity?
They allow rapid, non-specific recognition of pathogens
31
What are Toll-like receptors?
A family of PRRs that detect microbial components and initiate inflammatory signalling
32
Where are TLRs located in the cell?
On the cell surface and on endosomal membranes
33
Which TLR recognises LPS from Gram-negative bacteria?
TLR4
34
Which TLRs recognise Gram-positive bacterial components?
TLR1/TLR2 heterodimer
35
Which ligands are recognised by endosomal TLRs?
Viral ssRNA, dsRNA, and bacterial CpG DNA
36
What intracellular domain is shared by TLRs?
TIR (Toll–IL-1 receptor) domain.
37
What adaptor molecule is used by most TLRs?
MyD88
38
What is the outcome of TLR signalling?
Activation of inflammatory gene transcription and cytokine production
39
What role do dendritic cells play in adaptive immunity?
They activate naiive T cells
40
Where do dendritic cells capture antigen?
In peripheral tissues (e.g. skin)
41
Where do dendritic cells activate naiive T cells?
In lymph nodes
42
What is opsonisation?
Coating of pathogens with antibodies or complement to enhance phagocytosis
43
Which receptors on phagocytes recognise opsonised pathogens?
Fc receptors and complement receptors
44
Why does opsonisation increase bacterial killing?
It enhances uptake and triggers lysosome-phagosome fusion
45
How do some bacteria evade phagocytosis?
By resisting uptake or surviving inside phagocytes
46
How does adaptive immunity overcome bacterial evasion?
Through antibody- mediated opsonisation