12. Autoimmune Disease I Flashcards

(30 cards)

1
Q

What is the approximate number of people affected by autoimmune diseases in the UK?

A

Approximately 4 million people

This represents around 10% of the population.

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2
Q

How many different autoimmune diseases have been identified?

A

Around 80 different autoimmune diseases

Among these, 19 are the most prevalent.

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3
Q

What percentage of autoimmune diseases occur in women?

A

75% of autoimmune diseases

This statistic highlights the gender disparity in autoimmune conditions.

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4
Q

What is the fourth largest cause of disability in women?

A

Autoimmune diseases

These diseases significantly impact women’s health and quality of life.

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5
Q

In what demographic do autoimmune diseases often manifest?

A

People in the prime of their lives

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6
Q

How common is rheumatoid arthritis in the population?

A

Affects approximately 1 in 100 people

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7
Q

What is the normal function of the immune system?

A

To distinguish between self and non-self

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8
Q

What occurs in autoimmunity?

A

Immune cells attack the body’s own tissues

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9
Q

What two factors are required for autoimmunity to develop?

A

Genetic predisposition and environmental triggers

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10
Q

Name three environmental factors that can trigger autoimmunity.

A
  • Bacteria
  • Viruses
  • Toxins
  • Drugs

Epstein-Barr virus is linked to multiple sclerosis.

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11
Q

What genetic factors are often involved in autoimmunity?

A

MHC (Major Histocompatibility Complex) alleles

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12
Q

What are the three essential components for T cell activation?

A
  • MHC-peptide complex on antigen-presenting cell
  • T cell receptor (TCR) specific for that complex
  • Co-stimulatory signals

An example of a co-stimulatory signal is CD28 on T cell binding to B7 on APC.

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13
Q

What happens if any of the three components for T cell activation are missing?

A

T cells don’t become fully activated

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14
Q

What do activated helper T cells do?

A
  • Activate B cells to produce antibodies
  • Activate CD8+ cytotoxic T cells
  • Produce cytokines to regulate immune responses
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15
Q

What are the two classes of MHC molecules?

A
  • MHC Class I
  • MHC Class II
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16
Q

What is the function of MHC molecules?

A

To present peptides for T cell recognition

17
Q

What did Peter Doherty and Rolf Zinkernagel discover about T cells?

A

T cells must recognize both self MHC molecules and foreign antigens presented by MHC

18
Q

What is central tolerance?

A

The process where developing T and B cells are educated to not attack self

19
Q

Where does positive selection of T cells occur?

A

In the thymus

20
Q

What is the outcome of positive selection in T cell development?

A

Only T cells that can recognize self-MHC survive

21
Q

What happens during negative selection of T cells?

A

T cells that strongly react to self-antigens are eliminated through apoptosis

22
Q

What are the binding affinity outcomes for T cells?

A
  • No affinity: Cells die
  • Low affinity: Cells survive
  • Intermediate affinity: Become regulatory T cells
  • High affinity: Cells die
23
Q

What is peripheral tolerance?

A

Secondary protection mechanisms for self-reactive cells that escape central tolerance

24
Q

Name two key mechanisms of peripheral tolerance.

A
  • Lack of co-stimulation
  • Anergy
  • Regulatory T cells
  • Ignorance
25
What occurs during central B cell tolerance?
* Deletion of self-reactive B cells * Receptor editing of B cells
26
What happens to immature B cells with self-reactive B cell receptors?
They undergo apoptosis or receptor editing in bone marrow
27
What is peripheral B cell tolerance?
Mechanisms for self-antigens not present in bone marrow
28
Name two mechanisms of peripheral B cell tolerance.
* Reduced BCR expression * Anergy * Ignorance
29
What experimental evidence supports B cell tolerance?
Goodnow and Basten experiments with double transgenic mice
30
What are the scenarios leading to tolerance or autoimmunity?
* Strong interaction with self-antigens in bone marrow * Interaction with soluble self-antigens * Low-affinity interaction with self-antigens * No interaction with self-antigens