T Cells Flashcards

1
Q

Outline how endogenous antigens are made

A

Endogenous antigens made be derived from intracellular viral or cancerous proteins. Viruses infect cell and commandeer there machinery to make viral proteins (for viral replication). Cancerous cells have abnormal changes in DNA code, which cause these cells to build abnormal proteins.

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2
Q

Outline MHC 1 antigen processing

A

Antigenic proteins (viral/cancerous) are degraded in cytoplasm
Peptide loading of MHC 1 takes place in the endoplasmic reticulum

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3
Q

Outline MMHC 2 antigen processing

A

Antigen intake via phagocytosis into a phagolysosome.
Antigenic proteins are degraded in acidic phagolysosome
Peptide loading of MHC 2 takes place in phagolysosome

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4
Q

What are T cells

A

Lymphocytes that arise in the bone marrow (diving stem cells) and fully develop in thymus.
T cells express T cell receptor (TCR) with co receptors (either CD4 or CD8)
Recognise MHC/peptide complexes

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5
Q

Expand on the rearranging of T cell receptor DNA

A

Occurring in the thymus, the DNA regions that code for the T cell receptors are rearranged. This results in various T cells having various receptors, leading to diversity of T cell receipting capability throughout the body.
T cell clonal replication then multiplies the number of specific T cells within the body.

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6
Q

Outline antigen triggered T cell clonal replication

A

If a T cells TCR binds antigen and associated MHC complex with enough affinity, then T cell undergoes clonal expansion while retaining specific initial TCR sequence.

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7
Q

Outline the production of T cells

A

T cells begin as products of stem cell replication in bone marrow. Immature T cells then migrate to the thymus where they mature. T cell development and TCR gene rearrangement occurs in thymus. Screening process screens out self attacking T cells. After T cell education in thymus, mature T cells move onto lymphoid organs, blood, tissue.

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8
Q

Outline Thymic gene rearrangement

A

Immature T cells (thymocytes) rearrange the variable parts of their TCR genes in thymus.
Th rearrangement process is essentially random.
This ensures that individual T cells are unique in terms of their TCR. Creates diversity in T cell repertoire.

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9
Q

What are naive T cells

A

Mature T cells that have not seen an antigen

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10
Q

What is the main function of CD4 and CD8 co receptors

A

Work alongside T cell receptor, helping interact with correct MHC protein on antigen presenting cells

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11
Q

Outline the preferential binding of CD4 and CD8

A

CD4 preferentially binds with MHC 2
CD8 preferentially binds with MHC 1

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12
Q

What are effector T cells

A

Activated T cells

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13
Q

Outline CD4 T helper cell

A

Recognises MHC 2/ extracellular peptides
Helps B cell make antibodies
Helps CD8 T cell become cytotoxic (release of cytokine growth factors that activate CD8)

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14
Q

Outline CD8 T cell

A

Recognise MHC1/ intracellular peptide (viral/cancerous)
Develop into cytotoxic T lymphocytes/Cytotoxic T cell

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15
Q

Outline the conjoint activation of CD4 and CD8, especially in a viral sense

A

CD8 T cells activated by MCH1, however really need cytokines (produced by CD4 - also activated) to activate. Particularly for viral responses, multiple cells need to be activated. CD4 helper cell activates CD8 T cell

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16
Q

What is an activated CD8 cell called, and what mediates which cells they target

A

Cytotoxic C lymphocyte
MHC + virus peptide binding CD8 TCR

17
Q

What are memory T cells

A

T cell activation also results in formation of memory T cells
Memory CD4 or CD8 T cells reside in the body for long periods of time
Memory T cells become effector cells much quicker than naive T cells - lower threshold for activation

18
Q

Why are there large numbers of T cells with correct TCR

A

Because they are the result of cell decision, there are simply more of them with correct T cell receptor.
Only T cells with correct TCR undergo cell division during infection, resulting in large specificity.

19
Q

Do B cells make antibody

A

Yes