Immunology Flashcards

1
Q

Where are basophils and eosinophils found and what do they do?

A

Circulate in blood

Recruited to sites of infection

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2
Q

What do mast cells, basophils and eosinophils secrete?

A

Release chemicals such as histamine, heparin and cytokines

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3
Q

What do phagocytise cells do?

A

Ingest and kill Bactria and fungi

Clear debris from dead/dying tissues

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4
Q

Where are neutrophils found and what do they do?

A

Circulate freely in blood

Rapidly recruited into inflamed and infected tissues

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5
Q

What do monocytes/macrophages do?

A

Help limit inflammation
Tissue repair and wound healing
Involves in antigen presentation

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6
Q

What do dendritic cells do?

A

Mature and migrate to secondary lymphoid tissues and stimulate antigen presentation (adaptive immune response)

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7
Q

What are NK cells and what do they do?

A

Large granular lymphocytes
Kill tumour cells and virally infected cels
Kill anitbody bound cells/pathogens

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8
Q

What are B cells responsible for?

A

Production of antibodies

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9
Q

What is primary lymphoid tissue the site of?

A

Leukocyte development

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10
Q

What is secondary lymphoid tissue the site of?

A

Where adaptive immune responses are initiated

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11
Q

What is the lymphatic system?

A

System of vessels draining fluid from body tissues

Lymph nodes are initiated regularly along lymph vessels - remove pathogens and antigens from lymph

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12
Q

2 mechanisms of common cation in the immune system?

A

Direct contact

Indirect contact

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13
Q

What is the interaction between in direct contact?

A

Receptor:Ligand interactions

Receptor if immune cell, ligand of pathogen

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14
Q

What is indirect contact?

A

Production and secretion of cytokines

Injured tissue cells and activated immune cells can produce and secrete cytokines

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15
Q

What are cytokines?

A

Diverse collection of small proteins and peptides produced in response to infection

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16
Q

What is the general function of cytokines?

A

Coordinate immune system by ,ovulating behaviour of cells

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17
Q

Examples of cytokines?

A

Interferons
TNF
Chemotherapy
Interleukins

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18
Q

Functions of interferons

A

Antiviral functions

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19
Q

Function of TNF

A

Pro inflammatory

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20
Q

Function of chemokines

A

Control and direct cell migration

21
Q

Local response to infection

A
Rubor (redness)
Calor (heat)
Tumour (swelling)
Dolor (pain)
Functio laesa (loss of function)
22
Q

3 phases in response to invading pathogens

A

Recognition
Activation
Effector

23
Q

What happens in regonitiom phase?

A

PRRs (pattern-recognition receptors)

Pathogen associated mole

24
Q

IgA

A

2nd most abundant Ig type
Monomeric form - blood
Dimeric - great milk, saliva, tears, mucosal secretions

25
IgD
Extremely low levels in blood | Surface bound = BCR
26
IgE
Extremely low levels normally | Produced in response to parasitic infection and allergic responses
27
IgG
Most abundant Ig in plasma Actively transported across placenta 4 subtypes
28
IgM
Surface bound monomer = BCR 1st Ig type produced in an immune response ( pentamer - present only in plasma/secretions)
29
How are B cells activated?
Encounter with antigen within lymph nodes If signalled by T lymphocytes B cells rapidly proliferate Differentiate
30
Function of antibodies
Identify pathogens Recruit other immune components (complement, phagocytes, NK cells) Neutralise toxins Particularly important in defence against bacteria
31
Defect of haemopoetic stem cells
Reticular dysgenesis
32
Defects of lymphoid precursors
Severe combined immunodeficiency (SCID) | Failure of production of lymphocytes
33
Clinical features of SCID
``` Unwell by 3 months old Persistent diarrhoea Failure to thrive Continuous infections Unusual skin disease Family history of early infant death ```
34
How long does maternal IgG protect baby for?
3 months
35
Most common form of SCID
X-linked SCID Mutation of IL-2 receptor (inability to respond to cytokines)! Produces immature B cells
36
Treatment for SCID
Prophylactic - avoid infections (antibiotics, antifungals, no vaccine) - aggressive treatment of existing infections - antibody replacement (IV immunoglobulin) Definitive - stem cell transplant (sibling) - gene therapy
37
What is DiGeorge syndrome?
``` Chromosomal deletion Congenital heart defects Cleft palate Hypoparathyroidism Psychiatric disorders ```
38
Clinical presentation of DiGeorge syndrome
Funny looking kid - low set folded ears - high forehead - cleft palate, small mouth & jaw - hypocalcaemia - oesophageal atresia - T cell lymphophopenia - congenital heart disease
39
Investigations for DiGeorge syndrome
Absent or decreased T cells Normal or increased B cells Normal NK cell numbers
40
Management of DiGeorge syndrome
Prophylactic antibiotics Aggressive treatment of infection Immunoglobulin replacement T cell function improves with age
41
Disorders of T cell effector function
Cytokines production Cytotoxicity T-B cell communication
42
Infections caused by issues with IL12 gIFN network
TB Atypical mycobacteria BCG infection after immunisation Deep fungal infections (e.g. Aspergillus)
43
Where are mast cells found and what do they do?
Reside in tissues and protect mucosal surfaces
44
Clinical features of common variable immune deficiency
Recurrent bacterial infections Autoimmune disease Granulomatous disease
45
What does CRP show?.
Degree if inflammation
46
Functions of complement
``` Opsonisation Inflammation Chemotaxis Membrane attack complex Clearance of immune complexes ```
47
What is an antigen?
A substance which can cause an adaptive immune response by activating B cells and T cells
48
Where do adaptive immune responses occur?
Secondary lymphoid tissue