B and T Cells and MHC Flashcards

1
Q

How are T cells derived?

A

T cells derive from bone marrow stem cells. T cell precursor cells arrive in thymus and spend up to 7-21 days undergoing differentiation and proliferation into a mature, but antigen naive, phenotype.

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2
Q

Where do most T cells die?

A
  • About 5 x 107 cells are made in thymus every day
  • Only 2-4% of these cells leave thymus as mature T cells to populate lymph nodes etc. What happens to the rest? Thymus maintains same size.
  • Over 95% of thymocytes die in thymus. What is going on?
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3
Q

Describe the process of educating T cells

A
  • Small double positive thymocytes (CD4 and CD8) initially express low levels of the receptor they use to recognise antigen, the TcR.
  • Most of these TcRs won’t recognise your own Major Histocompatibility Complex (MHC) molecules (more on them later), so the T cells die because of a lack of ‘positive selection’.
  • Those cells that do see your own MHC go on to mature and express high levels of TcR. They then lose either CD4 or CD8 to become single positive cells.
  • During this latter stage the T cells also undergo ‘negative selection’, to eliminate T cells that see your own MHC with high affinity, ie which could become autoreactive T cells.
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4
Q

What does thymic education result in?

A

he release into the periphery

of cells that are ‘restricted’ to recognising your own MHC.

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5
Q

What is the MHC?

A

Major Histocompatibility Complex

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6
Q

Describe the structure of the T cell receptor

A

Almost like an immunoglobulin, but not quite

Made of alpha and beta polypeptide chains w variable and constant regions found extramembranously

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7
Q

Describe the structure of the TcR binding site

A

Very similar to an antibody

TcR and antibodies are evolutionary related. Both are members of the ‘Immunoglobulin Superfamily’ .

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8
Q

How are TcR genes varied?

A

TcR undergo chromosomal rearrangement, similar to antibody genes

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9
Q

What is a basic summary of TcR - MHC interaction?

A
  • Antibodies ‘see’, ie bind the antigen they were raised against on its own, that is, free in solution, or maybe in a membrane.
  • But, the TcR only ever recognises an antigen when it is bound by an MHC molecule. In other words TcR recognition of antigen is ‘MHC- restricted’
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10
Q

What type of molecules do MHC molecules bind?

A

peptides

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11
Q

Why do MHC molecules bind peptides?

A

Protein antigen in cell is processed by breakdown of antigen protein can then be presented on the MHC externally

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12
Q

What are the two types of MHC molecules?

A
MHC class I
MHC class II
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13
Q

Describe MHC class I

A
  • Two chains, a heavy chain, and a small !2- microglobulin
  • Upper surface forms a groove into which small 8-10 amino acid peptides sit.
  • Expressed on almost every cell in your body, though at low levels in some (eg CNS)
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14
Q

Describe MHC class II

A
  • Two chains, alpha and beta, both membrane bound
  • Upper surface forms groove into which longer peptides, over 20 amino acids sits.
  • Expression more limited to specialised antigen presenting cells and immune cells, eg macrophages, dendritic cells, B and T cells.
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15
Q

What are the different MHC classes recognised by?

A

MHC class I is recognised by CD8 T cells, MHC class II is seen by CD4 T cells

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16
Q

What is a summary of the two types of MHC?

A
  • The two MHC types pickup peptides from very different environments.
  • MHC class I picks up peptides mostly derived from the internal contents of your cells, eg cytoplasm and nucleus.
  • MHC class I meets peptides in the endoplasmic reticulum (ER)
  • MHC class II picks up peptides derived from external sources, ie outside your cells
  • MHC class II molecules meet peptides in endosomes.
17
Q

How many forms may MHC molecules take?

A

An absolute ton, MHC molecules are highly polymorphic

18
Q

Where are the polymorphisms of MHC located?

A

In the peptide-binding groove

This means that each different MHC molecule will present different Peptides to the immune system.

19
Q

Why is it important to understand MHC molecules?

A

Autoimmunity: many MHC molecules are associated with autoimmune diseases
Transplantation: the major factor in graft rejection is MHC disparity
Cancer. A multitude of tumour lines from the different stages of B and T cell development.
Acute lymphoblastic leukemia
Thymoma
Acute lymphoblastic leukemia
Adult T cell leukemia, Chronic lymphocytic leukemia
Hodgkin’s disease
Superantigens - toxic shock syndrome
DiGeorge’s syndrome - failure to develop thymic epithelia, few T cells
Severe combined immunodeficiency (SCID)
Bare lymphocyte syndrome

20
Q

What is the impact of MHC molecules on transplantation?

A

The major factor in graft rejection is MHC disparity. Why? Your own T cells are educated to see your own MHC molecules. Anyone else’s are similar, but just different enough to cause a response. Thus MHC matching is crucial to improve graft survival. Even if a full match is obtained, you have enough different peptides (called minor transplantation antigens) to trigger a slow graft rejection, so immunosuppression still required.

21
Q

What are some autoimmune diseases associated with MHC molecules?

A

Ankylosing spondylitis and HLA-B27. Multiple sclerosis and HLA-DR2. Type I IDDM and HLA-DR3/DR4. Rheumatoid arthritis and HLA-DR4.