Immunopathology Flashcards

Lectures: -Week 4, day 1, lecture 1: Immunopathology II - Autoimmunity -Week 4, day 1, lecture 2: Immunopathology II - Allergy, hyperreactivity & celiac disease -Week 4, day 3, lecture 1: Immune pathology - Immune deficiency -Week 4, day 3, lecture 2: Immune pathology - Lymphoproliferation

1
Q

What is auto-immunity?

A

The failure of an organism in recognizing its own constituent parts as self, leading to an immune response against its own cells and tissues

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2
Q

True or false: auto-immune processes always cause disease

A

False; it is a physiological process with several functions:
1. Clearance of immune complexes and cell debris
2. Regulation of the immune response
3. Immune surveillande of dysplastic/neoplastic cells

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3
Q

When is auto-immunity pathological?

A

When disease arises due to autoreactivity

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4
Q

What is M. Graves?

A

A hypertyrhoid auto-immune disease, caused by activating antibodies against the TSH-receptor

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5
Q

What is M. Hashimoto?

A

A hypothyroid auto-immune disease, caused by antibodies and autoreactive T-cells against thyroid antigens

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6
Q

What are Witebsky’s postulates?

A

A set of postulates that describes the characteristics of auto-immune disease:
-Presence of auto-antibodies and/or autoreactive T-cells that are:
1. Disease-associated
2. Specific for the affected organ
3. Present at the site of tissue damage
4. Reflective of disease activity (higher level = more activity)
5. Cause for disease when transferred to a second host
6. Cause for disease when induced by immunsation
-Reduction of auto-immune response leads to improvement

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7
Q

True or false: auto-immune diseases always follow Witebsky’s postulates

A

True; auto-immune diseases always follow SOME of Witebsky’s postulates, but not always all of them

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8
Q

What is the prevalence of auto-immune disease in (Western) society?

A

~3%

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9
Q

What are the peaks of onset of auto-immune disease? (2)

A
  1. Puberty
  2. Retirement
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10
Q

Auto-immune disease is more common in [men/women]. Why?

A

Women; sex hormones are thought to strengthen immune response

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11
Q

What is the effect of pregnancy on auto-immune disease?

A

Pregancy shifts the Th1/Th2 balance & immune balance -> can aggravate or subdue auto-immune systems during pregnancy

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12
Q

Which auto-immune disease characteristically is (far) more present in men?

A

Ankylosing spondylitis (M. Bechterew)

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13
Q

What are the thymic/central tolerance mechanisms for T-cells? (2)

A
  1. Positive/negative selection
  2. Receptor editing
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14
Q

What are the peripherhal tolerance mechanisms for T-cells? (4)

A
  1. Segregation -> tissue layers that prevent T-cells from reaching certain sites (such as immune-privileged sites)
  2. Anergy
  3. Apoptosis
  4. Suppression by Tregs
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15
Q

What is anergy? How is it induced?

A

A state of non-reaction caused by stimulation of the TCR in absence of co-stimulatory/cytokine signals

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16
Q

What is an example of an immune-privileged site?

A

Eye

17
Q

What are the three main mechanisms that can lead to breakdown of tolerance?

A
  1. Inappropriate access of auto-antigens to APC and/or expression of MHC/co-stimulation
  2. Loss of T-reg cells
  3. Molecular mimicry
18
Q

How can inappropriate access of APC’s and T-cells to auto-antigens come to be? (2)

A
  1. Infection
  2. Tissue damage
19
Q

What can cause a loss of Treg cells?

A
  1. Cytotoxic drugs
  2. FoxP3 mutation
20
Q

Why does a FoxP3 mutation increase susceptibility to auto-immune disease?

A

This is an important transcription factor in the development of Treg cells

21
Q

What is molecular mimicry?

A

Cross-reactivity of antibodies or T-cells that were originally aimed at a pathogen

22
Q

What is an important example of molecular mimicry?

A

Guillain-Barré

23
Q

What is the most important genetic factor that modulates the (susceptibility to) auto-immune disease?

A

HLA-serotype -> some serotypes are associated with a higher or lower chance of certain auto-immune disease

24
Q

In addition to the HLA-type, which genetic factors have an influence on (susceptibility to) auto-immune disease?

A

Genes involved in the immune system, such as AIRE (negative selection), FoxP3 (Treg development), Fas (defective apoptosis of auto-reactive cells), C1q (defective clearance of immune complexes and apoptotic cells)

25
Q

How does a mutation in AIRE cause auto-immune disease?

A

Decreased expression of self-antigens in the thymus -> defective negative selection of auto-reactive T-cells

26
Q

How does a mutation in CTLA4 cause auto-immune disease?

A

Failure of T-cell anergy and reduced activation threshold of auto-reactive T-cells

27
Q

How does a mutation in FoxP3 cause auto-immune disease?

A

Decreased function of Treg-cells

28
Q

How does a mutation in FAS cause auto-immune disease?

A

Failure of apoptotic death of auto-reactive cells

29
Q

How does a mutation in C1q cause auto-immune disease?

A

Defective clearance of immune complexes and apoptotic cells

30
Q

Which four types of auto-reactions can be identified?

A
  1. Type I: degranulation of mast cells with (auto-reactive) IgE
  2. Type II: presence of antibodies against cell-surface or matrix antigens
  3. Type III: deposition of immune-complexes in tissue
  4. Type IV: T-cell mediated disease
31
Q

What are the two main strategies to treat auto-immune disease? (2)

A
  1. Replacement of function of damages organs
  2. Immunosuppression/immunomodulation
32
Q

What drugs are available to suppress T-cells? (6)

A
  1. Corticosteroids
  2. Azathioprine
  3. Cyclophosphamide
  4. Cyclosporine
  5. Alemtuzumab (anti-CD52)
  6. Influximab/adalimumab (anti-TNFα)
33
Q

What drug is often used to suppress B-cells?

A

Rituximab (anti-CD20)

34
Q

Which strategies can be used to suppress/modulate auto-antibodies? (2)

A
  1. IVIG
  2. Plasmapheresis