Autoimmunity Flashcards

1
Q

What is the range of autoimmune disorders?

A

➝ systemic

➝ organ specific

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2
Q

What are 2 examples of an organ specific autoimmune disease?

A

➝ Graves disease

➝ Type 1 diabetes

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3
Q

What is Graves disease?

A

➝ an antibody response to the TSH receptors in the thyroid

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4
Q

Why do you get bulging eyes in Graves disease?

A

➝ Low level of TSH receptors in the fibroblasts in the eye

➝ immune deposition of antibodies in the eye

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5
Q

What are the 6 types of HLA B27- associated spondyloarthropathies?

A
➝ Ankylosing spondylitis
➝ undifferentiated spondyloarthropathy
➝ reactive arthritis
➝ psoriatic arthritis 
➝ urethritis
➝ iritis
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6
Q

What is usually associated with HLA B27- associated spondyloarthropathy?

A

➝ bowel inflammation

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7
Q

What is the cause of systemic lupus erythematous (SLE)?

A

➝ Autoantibodies to nuclear antigens :

➝ double stranded DNA

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8
Q

What are the 8 signs of SLE?

A
➝ discoid lesions
➝ alopecia
➝ butterfly rash
➝ pericarditis
➝ arthritis
➝ proteinuria
➝Raynauds 
➝ mucus membrane ulceration
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9
Q

What is autoimmunity?

A

➝ Failure of the regulatory controls in the immune system that prevent it attacking itself

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10
Q

What is central tolerance?

A

➝ Destroy self-reactive T or B cells before they enter the circulation

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11
Q

What is peripheral tolerance?

A

➝ Destroy or control any self reactive T or B cells which do enter the circulation

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12
Q

How does central tolerance of B cells occur?

A

➝ Immature B cells in bone marrow encounter an antigen in a form which can cross-link their IgM then apoptosis is triggered

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13
Q

What happens if a T cell binds to MHC too weakly?

A

➝ it may not be enough to allow signalling when foreign peptides are in the groove

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14
Q

What happens if a T cell binds to MHC too strongly?

A

➝ it may allow signalling irrespective of whether self or foreign peptide is in the groove

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15
Q

What types of T cells get selected in the thymus and which get destroyed?

A

➝ T cells that don’t bind to any MHC - death by neglect
➝ T cells that bind to MHC too strongly - apoptosis triggered- negative selection
➝ T cells that bind self MHC weakly - signal to survive

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16
Q

How do T cells in the thymus encounter MHC bearing peptides from other parts of the body?

A

➝ A specialised transcription factor allows thymic expression of genes that are expressed in peripheral tissue

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17
Q

What is AIRE and what is its function?

A

➝ (autoimmune regulator)

➝ it promotes self tolerance by allowing the thymic expression of genes from other tissues

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18
Q

What do mutations in AIRE result in?

A

➝ multi organ autoimmunity

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19
Q

What are the three steps in peripheral tolerance?

A

➝ Ignorance
➝ anergy
➝ regulation

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20
Q

Why does the ignorance step happen in peripheral tolerance?

A

➝ the antigen may be present in too low a concentration to reach the threshold for T cell receptor triggering
➝ e.g immunologically privileged sites such as the eye or the brain
➝ T cells will not come across the antigen

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21
Q

What is anergy?

A

➝ Exposure to antigen without appropriate co-stimulatory signals

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22
Q

How does anergy occur?

A

➝ Naive T cells needs co-stimulatory signals to be activated
➝ most cells lack co-stimulatory proteins and MHC class II
➝ if a naive T cell sees its MHC/peptide without appropriate co-stimulation it becomes anergic

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23
Q

What does anergic mean?

A

➝ less likely to be stimulated in the future even if co-stimulation is present

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24
Q

What cells are involved in the regulation step in peripheral tolerance?

A

➝ Treg cells

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25
Q

How do Treg cells work?

A

➝ The Treg cells bind to an antigen on an APC they can send a negative signal to any other cells that are recognising antigens on that cell via TGF beta and IL-10

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26
Q

What two conditions cause a varying of Treg numbers?

A

➝ Cancer - increased Treg

➝ autoimmune - decreased Treg

27
Q

What do Treg cells express?

A

➝ Transcription factor FOXP3

28
Q

What do mutations in FOXP3 lead to?

A

➝ IPEX disease

➝ immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome

29
Q

On what chromosome is MHC located?

A

➝ chromosome 6

30
Q

How many genes are there for MHC class I and II?

A

➝ 3 for each

31
Q

What is MHC associated with in terms of disease?

A

➝ the most disease compared to other regions in the genome

32
Q

In what gender is SLE more common in?

A

➝ 10x more common in females than males

33
Q

In what gender is MS more common in?

A

➝ 10 times more common in females than males

34
Q

In what gender is diabetes common in?

A

➝ equally common in both

35
Q

in what gender is ankylosing spondylitis more common in?

A

➝ 3 times more common in males than females

36
Q

What is the hygiene hypothesis?

A

➝ If you keep a (non obese diabetic mouse) in a pathogen free environment it doesn’t get diabetes

37
Q

What 3 diseases become more apparent when you move from a rural environment to a more urban one?

A

➝ type 1 diabetes
➝ MS
➝ SLE

38
Q

What disease is smoking linked with and what is the proof?

A

➝ rheumatoid arthritis

➝ 13 pairs of identical twins where 1 of the pair smokes, 12/13 cases the twin with arthritis was the smoker

39
Q

What are the 4 things that can trigger a breakdown of self tolerance?

A

➝ Loss of or a problem with regulatory cells
➝ release of a sequestered antigen
➝ modification of self
➝ molecular mimicry

40
Q

What is citrulline?

A

➝ an amino acid not coded for by DNA

41
Q

What is citrullination?

A

➝ arginine converted into citrulline as a post translational modification

42
Q

What enzyme causes citrullination?

A

➝ peptidylarginine deaminase (PAD)

43
Q

What can citrullination be increased by?

A

➝ inflammation

44
Q

What link does citrulline have with rheumatoid arthritis?

A

➝ Autoantibodies to citrullinated proteins are seen in rheumatoid arthritis

45
Q

How is rheumatic fever caused?

A

➝ Disease is caused by infection with streptococcus pyogenes

➝ antibodies to the streptococcus cell wall antigens may cross react with cardiac muscle

46
Q

How can hyperthyroidism arise?

A

➝ autoantibodies bind TSH receptor and stimulate it

47
Q

What is Hashimotos disease?

A

➝ autoantibodies bind TSH receptor and cause inflammation

48
Q

What happens in myasthenia gravis?

A

➝ Autoantibodies bind to AcH receptor and block the ability of Ach to bind
➝ leads to receptor internalisation and degradation
➝ results in muscle weakness

49
Q

What types of autoimmune diseases can be transferred across the placenta and why?

A

➝ Diseases mediated by IgG

➝ IgG is small enough to cross the placenta

50
Q

What are the 5 diseases that can be transferred across the placenta?

A
➝ Myasthenia gravis
➝ Graves disease
➝ Thrombocytic purpura
➝ Neonatal lupus rash/congenital heart block 
➝ Pemphigus vulgaris
51
Q

How can you β€˜cure’ a baby from an autoimmune disease transferred from the mother?

A

➝ Plasmaphorese the baby and remove all the IgG

52
Q

Which cytokine induces self destruction?

A

➝ TNF alpha

53
Q

What are the 4 ways in which T cells are involved in autoimmune pathologies?

A

➝ direct killing by CD8+ and cytotoxic T cells
➝ self destruction by TNF alpha
➝ recruitment and activation of macrophages leading to bystander tissue destruction
➝ CD4 cells can activate antibodies and cytotoxicity

54
Q

What two conditions are caused by T cells malfunctioning?

A

➝ Insulin dependent diabetes

➝ Multiple sclerosis

55
Q

What do TH17 helper cells produce?

A

➝ IL-17

56
Q

What is the function of TH17 cells?

A

➝ Produce cytokines which are involved in the recruitment, migration and activation of immune system

57
Q

What are 3 therapeutic strategies for autoimmune diseases?

A

➝ Anti-inflammatories
➝ T & B cell depletion
➝ Therapeutic antibodies

58
Q

What are two examples of anti-inflammatories?

A

➝ NSAID

➝ corticosteroids

59
Q

What is used to deplete T & B cells in rheumatoid arthritis?

A

➝ anti CD4

➝ anti CD20

60
Q

What are two therapeutic antibodies?

A

➝ anti TNF

➝ anti VLA-4

61
Q

What is the function of anti VLA-4?

A

➝ blocks adhesion

62
Q

Why does anti TNF only work for a short while?

A

➝ the body makes antibodies to the antibodies

63
Q

What drug increases Treg?

A

➝ glatiramer acetate