Basic Immunology Flashcards

1
Q

What cells make up the innate immune system?

A

neutrophils, monocytes, macrophages, mast cells and natural killer cells

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2
Q

How does the innate immune system detect infection?

A

pathogen associated molecular patterns (PAMPs) bind toll like receptors

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3
Q

How does the innate immune system detect cell damage?

A

damage associated molecular patterns (DAMPs) bind to DAMP receptors

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4
Q

Which chemokines and cytokines are released when TLRs and DAMP receptors are activated?

A

IL-1beta, TNFalpha, IL-6, CXCL8, IL-12

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5
Q

What is the outcome of the complement system?

A

the membrane attack complex

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6
Q

How is the complement system activated?

A

either via the classical pathway, the lectin pathway or the alternative pathway

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7
Q

What is the central junction for all the complement pathways?

A

C3 convertase

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8
Q

How is the classical complement pathway activated?

A

antigen-antibody binding

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9
Q

How is the lectin complement pathway activated?

A

mannan-binding lectin binds mannose on pathogen surfaces

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10
Q

What happens to patients that have a deficiency of C1q, C1r, C1s and C4?

A

immune complex deposition in tissues leading to glomerulonephritis

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11
Q

What happens to patients that have a deficiency of late complement pathway?

A

can’t make a membrane attack complex so are immunodeficient and get infections particularly to neisseria meningitidis

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12
Q

What happens to patients that are deficient in C1 esterase inhibitor?

A

hereditary angioneurotic oedema

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13
Q

What is complement induced HUS?

A

either genetic or autoimmune disease leading to deficiency of complement regulatory proteins which causes renal failure and organ failure

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14
Q

How do you differentiate complement induced HUS from TTP and infection induced HUS?

A

ADAMTS13 normal, shiga toxin negative

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15
Q

How do you treat complement induced HUS?

A

eculizumab - a monoclonal antibody which blocks cleavage of C5 - however this means that can’t make MAC so need to be vaccinated against neisseria

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16
Q

Where do you find MHC I?

A

on all nucleated cells

17
Q

Where do you find MHC II?

A

on antigen presenting cells, dendritic cells, B cells and macrophages

18
Q

What is the role of the thymus?

A

in late fetal life all T cells go to the thymus where thymic epithelial cells express most self peptides - if there is binding then those T cells undergo apoptosis

19
Q

What is AIRE?

A

a transcription factor in thymic epithelial cells for expression of self peptides

20
Q

What is required for T cell clonal proliferation?

A

need antigen to presented by MHC, need second activating signal (CD40, CD80, CD86)

21
Q

What is the role of CD4 T cells?

A

recruit and activate innate leukocytes

22
Q

What is the role of CD8 T cells?

A

kill targeted cells/microbes by granzyme and perforins

23
Q

What are the 4 types of CD4 T cells?

A

TH1, TH2, TH17 and T reg

24
Q

What is the role of TH1?

A

activate macrophages, induces B cells to produce opsonising antibodies

25
Q

What is the role of TH2?

A

activates B cells to make neutralising antibodies

26
Q

What is the role of TH17?

A

protects against intracellular pathogens e.g. candida

27
Q

What is the role of Treg?

A

secretes cytokines (IL-10 and TGF beta) with immunosuppressive properties

28
Q

What is the role of IgM?

A

complement activation

29
Q

What is the role of IgG?

A

opsonisation and phagocytosis, complement activation

30
Q

What is the role of IgE?

A

immunity against helminths, mast cell degranulation

31
Q

What is the role of IgA?

A

mucosal immunity