Introduction Flashcards

1
Q

What is the immune system?

A

Molecules, cells and tissues that mediate immune responses

Lymphatic system, blood, interaction of immune organs

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

What tissues are associated with the immune system?

A

Lymph node, lymphatics, spleen, bone marrow, thymus

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

What molecules are associated with the immune system?

A

Complement- system of soluble serum proteins
Cytokines- immune messenger hormones (chemokines- specialise in making cells move)
Antibodies- secreted molecules bind to pathogens (adaptive)

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

What cells types are associated with the immune system?

A

Leukocytes- all immune cells/ white blood cells
Innate- macrophages, dendritic, neutrophils, eosinophils, basophils, mast
Adaptive- T cells, B cells, lymphocytes

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

Where are immune cells made?

A

Bone marrow and thymus

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Where do adaptive immune cells spend most of their time?

A

Lymph nodes and spleen

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

What is the purpose of lymphatics?

A

Drainage for periphery/ scanning for danger
Lymph nodes at lymphatic junctions
Drain into subclavian veins/ blood via thoracic duct

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

What are lymph nodes?

A

Highly organised accumulations of immune cells at lymphatic junctions
Swell during infection- lymphadenopathy

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

What is the difference between primary and secondary lymphoid organs?

A

Primary- immune cells are made, bone marrow- T cells mature in thymus (exported precursor)
Secondary- where immune responses are initiated, lymph nodes and spleen, tonsils appendix and Peyer’s patches in the gut

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

List barriers to prevent entry of extracellular pathogens

A

Physical- skin (dead so virus cannot replicate), gut epithelium (rapid turnover)
Chemical- low pH of skin, vagina and stomach
Flushing- tears, sweat, mucus
Antimicrobial peptides- small proteins directly toxic to bacteria, present in many secretions
Competitive- commensal bacteria out compete dangerous bacteria

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

What do virally-infected cells release?

A

IFN alpha and beta

Induces antiviral state in neighbouring cells

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

What happens in an anti-viral state?

A

Upregulate antiviral proteins (IFNs) and antigen presentation
Downregulate everything else by degrading mRNA and inhibiting protein translation factors (suppress viral proliferation)

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

How can an antiviral state be mimicked in a clinical setting?

A

Synthetic IFN a administration is highly effective in Hepatitis B virus infection

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

What are the pros of an immune system?

A

Protect against infection, immunity to reinfection/ vaccination response, kills mutated tumour cells, higher risk of cancer after transplants due to immunosuppression

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

What are the cons of an immune system?

A

Energy intensive, wasteful, causes disease- allergy (hay fever, asthma, eczema), autoimmunity (MS, Rheumatoid arthritis, Lupus), inflammatory bowel diseases
Mediates transplant rejection

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

What are pathogens?

A

Bacteria/ virus/ fungus/ protozoa/ helminth parasites
Intracellular and extracellular
Diversity in size and type

17
Q

What is danger?

A

Signals indicating there is harm to the body, and/or infectious agents and present, recognised by innate immune response

18
Q

How does the immune system distinguish between self and non-self?

A

Recognise own proteins- no attack
Kill non recognisable cells
Recognised by adaptive immune response

19
Q

What are the types of danger signals?

A

PAMPs- Pathogen Associated Molecular Patterns
- types of molecules only produced by infectious against and not host tissue
- Bacterial cell wall constituents (LPS)
DAMPs- Damage Associated Molecular Patterns
- Molecules released from injured cells
- DNA, RNA, ATP, breakdown products of extracellular matrix

20
Q

What is the difference between apoptosis and necrosis?

A

Apoptosis- programmed cell death, caspases activated, fragmentation of DNA, blebbing of membrane, phagocytosis, non-inflammatory
Necrosis- uncontrolled cell death, cell ruptures, contents release, highly inflammatory (DAMPs), mechanical damage from pathogen bursting out

21
Q

What are PRRs?

A

Pattern Recognition Receptors for PAMPs and DAMPs
Toll-like Receptors
TLR3- binds double stranded RNA in viruses
TLR4- bind LPS
TLR5- binds flagellin (flagellated bacteria)

22
Q

How is negative selection used in the immune system?

A

Different T and B cells, develop randomly (wasteful)
Kills those that react to self antigens
Mature adaptive immune cells

23
Q

What is the difference between adaptive and innate immune responses?

A

Innate- detects danger, rapid and generic response, communicates danger to adaptive
Adaptive- differentiates between self and non-self, slow and highly specific response, memory to antigens it has seen before

24
Q

What are the different strengths of immune response?

A

Susceptibility, Immunity, Immunopathology
Old/ young general susceptible
Cytokine storm- overactive immune response can kill

25
Q

What happens when the immune responds to something it shouldn’t?

A
  • Harmless environmental molecules (allergy) o self (autoimmunity)
  • Fatal anaphylactic shock/ hard to treat