Immunology Flashcards

(55 cards)

1
Q

IL associated with pyrexia

A

IL-1
IL-6

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2
Q

IL associated with neutrophil chemotaxis

A

IL-8

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3
Q

IL associated with B cell differentiation

A

IL-6

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4
Q

Site of action of IL-1
Action

A

Macrophages
Fever

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5
Q

Site of action of IL- 8
Action

A

Macrophages
Neutrophil chemotaxis

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6
Q

Site of action of IL-6
Action

A

Macrophages
Fever
B-cell differentiation

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7
Q

Mastocytosis
- What is it?
- What are the symptoms?

A

= proliferation of mast cells, neoplasm
Symptoms of carcinoid + urticaria

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8
Q

Marker in hereditary angioedema
Deficiency

A

C4 (because we have been there BEFORE)
Deficient = C1
C1 = vascular permeability > leaky vessels

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9
Q

CD4 T cells
- Express
- Also known as

A

MHC Class II
T helper cells

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10
Q

CD8 T cells
- Express
- Also known as

A

MHC Class I
Cytotoxic T cells

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11
Q

Further subdivision of CD4 cells
- How can they be told apart?

A

Th1 and Th2 cells
Classification depends on cytokines released
Th2 = humoral immunity (cytokines focus on Ab release)
Th1 = cell mediated immunity (cytokines focus on killing T cells)

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12
Q

How does IL-1 mediate the sepsis response?

A

Activates platelet activating factor, prostaglandin and nitric oxide
= potent vasodilators

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13
Q

Action of IL-5

A

Production and activation of eosinophilsA

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14
Q

Action of G-CSF

A

Allows development and activation of neutrophils

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15
Q

Action of TNF-alpha

A

Fever
Macrophage activation

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16
Q

Action of INF-gamma

A

Activation of macrophages

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17
Q

Cytokines which result in fever (3)

A

IL-1
IL-6
TNF-alpha

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18
Q

Action of INF-alpha

A

Activates macrophages

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19
Q

What activates the classical complement pathway?

A

IgM antibodies
IgG antibodies

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20
Q

What activates the alternative complement pathyway?

A

IgA
Endotoxin - LPS released from lysis of bacterial cell wall

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21
Q

Complement deficiency associated with immune complex disease
- Examples (3)

A

C2 and C4
- SLE, HSP, glomerulonephritis

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22
Q

Complement deficiency in recurrent infections

A

C5-C9

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23
Q

Alternative pathway

24
Q

Classical pathway

A

C1 > C4 > C2 > C3 > C5-9

25
Which antibody is the most abundant?
IgG
26
Can IgG cross the placenta?
Yes - hence issue with anti-D IgG antibodies in future pregnancy
27
Monomer antibodies (2)
IgG IgD
28
Pentamer antibody
IgM
29
Which antibody activates the alternative complement pathway?
IgA
30
Autoimmune haemolytic anaemia - Cold - Warm
Cold = IgM because cold is Miserable: intravascular Warm = IgG
31
Cryoglobulinaemia Type 1 Type 2 Type 3
Type 1 = monoclonal Type 2 = mixed monoclonal, polyclonal Type 3 = polyclonal
32
Association with Type 1 cryoglobulinaemia (2)
Myeloma, Waldenstroms - one clonal cell proliferating
33
Association with Type 2 cryoglobulinaemia (2)
Hepatitis C, Lymphoma
34
Type II hypersensitivity - problem - example (5)
Cell bound = antibody binds to cell surface e.g. autoimmune haemolytic anaemia, transfusion reaction, post-streptococcal glomerulonephritis, goodpastures, ITP
35
What type of hypersensitivity is Grave's disease?
Type II - TSH antibody binds to receptor, causing thyroid effects
36
Type III hypersensitivity - problem - example (4)
Immune complex = antibodies, free antigen and complement bind together to form complexes e.g. drug induced haemolytic anaemia, hypersensitivity pneumonia, malaria, SLE
37
Direct Coomb's Test - aim of test - example
Aim = looking for antibodies bound to red blood cells - AIHA - will be positive
38
Indirect Coomb's Test - aim of test - application
Looking for free antibodies in serum e.g. prior to transfusion, pregnancy for anti-D/other sensitising antibodies
38
What mediates hyperacute organ rejection?
B cell mediated - antibodies attack and destroy graft - Present due to previous sensitisation event
39
What mediates acute organ refection?
T cell mediated - T cells migrate out of graft, processed then invade
40
Pathogenesis of graft vs host disease
Donor lymphocytes attack antigen of recipient
41
B cell only disorders (4)
IgA deficiency Common variable immunodeficiency Bruton's Hypogammaglobulinaemia
42
Infection pattern in B cell disorders
Pyogenic bacteria Yeasts Giardia
43
Bruton's immunodeficiency - genetics - presentation age - problem
X-linked inheritance Under 6 months at presentation No B cells present
44
Combined B cell and T cell deficiencies (3)
Severe combined immunodeficiency Ataxic Telangiectasia Wiskott-Aldrich
45
Ataxic Telangiectasia - genetics - presentation (4)
Autosomal recessive Cerebellar ataxia, occular telangiectasia ENT, chest infections
46
Wiskott-Aldrich Syndrome - genetics - infection
X-linked recessive Pyogenic infections
47
Infection pattern in T cell disorders
Opportunistic infections
48
T cell disorder (1)
DiGeorge Syndrome
49
DiGeorge syndrome - genetic mutation - pathogenesis - presentation (3)
22q11 deletion - part of long arm Ch 22 is missing - Absence of a thymus due to issue with 3rd/4th pharyngeal pouch Hypoparathyroidism, CV problems, opportunistic infections
50
Infection pattern in neutrophil disorders
Gram -VE bacteria Staph aureus Viral infections Aspergillus
51
Chronic Granulomatous Disease - genetics - pathogenesis - when presents?
X-linked Defect in NADPH oxidase axis Presents in first 2 years of life
52
What kind of hypersensitivity reaction is ITP?
Type II - antibodies bind to platelets
53
Function of IgD antibodies
Activate B cells
54
Hyperacute transplant rejection mediated by which antibody?
IgG