Lymphocytes Identification, Tolerance, and Circulation Flashcards

1
Q

What surface molecules distingush T and B cells apart?

A

B cells have a B cell receptor for binding to an antigen and t cells have a t-cell receptor that needs a CD3 molecule for signalling

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2
Q

How are T and B cells identified (since you cannot distinquish normally with a microscope)?

A

flocytometry - the antibody molecules are coated with flourecent labels so once they bind to the T and B cells you are able to distinguish them

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3
Q

What is the difference between the primary and secondary response?

A

the secondary response has a shorter lag time, stronger titer, and higher affinity for binding

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4
Q

Define hybridoma.

A

a plasma cell tumor with a b cell that secretes a monoclonal antibody to recognize only 1 epitope

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5
Q

What is central tolerance?

A

when an immature lymphocyte meets its antigen (self-antigen) in the generative lymphoid tissues

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6
Q

What happens when an immature lymphocyte meets its antigen in primary lymphoid tissue?

A

die by apoptosis or follow a different route if it is a B cell or CD4 t cell

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7
Q

If it is a B cell, what happens when an immature lymphocyte meets its antigen in primary lymphoid tissue?

A

it may edit its antigen receptor to recognize a different antigen

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8
Q

If it is a CD4 T cell, what happens when an immature lymphocyte meets its antigen in primary lymphoid tissue?

A

it may become a regulatory T cell which supresses the T cell responses to the antigen

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9
Q

What is peripheral tolerance?

A

when a mature naive lymphocyte recognizes its antigen in the absense of danger signals out in the tissues

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10
Q

If a mature naive lymphocyte recognizes its antigen in the absence of danger what happens?

A

die by apoptosis, become anergic, or be supressed

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11
Q

What is IgM’s role in B cell development?

A

in bone marrow, IgM is on the naive B cell surface, if it does not recognize its antigen it passes to the next test

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12
Q

If the B cell does not recognize its self antigen, what happens?

A

it will mature, IgD will be put on its membrane and become a naive mature B-cell

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13
Q

Where does T cell tolerance develop?

A

in the thymus

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14
Q

What is positive selection of T cells?

A

if they recognize MHC I and MHC II they live, of not they die and are useless

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15
Q

What is negative selection of T cells?

A

if they recognize their own peptide in the MHC groove they die, if not they live; recognition here is bad

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16
Q

Through T-cell tolerance, what is the outcome if they pass the test?

A

they recognize self MHC I and MHC II, do not recognize their self peptide, and lose either CD4 or CD8 (whichever they do not need)

17
Q

What is the role of thymic epithelial cells and APCs in the thymus?

A

they present self peptides on MHC I and MHC II

18
Q

How does the thymus change as the individual ages and how does that effect immunity?

A

the thymus involutes (gets smaller) and there is an increase in infectious and autoimmune diseases, and cancers

19
Q

How do naďve lymphocytes and memory lymphocytes circulate in the blood stream and lymph system differently?

A

Memory lymphocytes can exit at interstitial space/tissues where infection is, where as immature lymphocytes have to go to the LNs

20
Q

What are high endothelial venules?

A

specialized venules that are the sites of lymphocyte migration from the blood into the stroma of secondary lymphoid tissues

21
Q

What is the structure of high endothelial venules?

A

lined with endothelial cells that produce into the vessel lumen

22
Q

What do the endothelial cells of high endothelial venules do?

A

express unique adhesion molecules for binding of naďve and central memory B and T cells

23
Q

What are the adhesion molecules that the endothelial cells of high endothelial venules express?

A

selectins and integrins

24
Q

How does the structure of lymphoid tissues maximize the opportunity for lymphocytes to meet their antigen and interact with one another?

A

the dendritic cells in the lymphoid tissues catch antigens so that when the lymphocytes circulate to the lymph tissue they have a higher chance of meeting their antigen in these areas due to the high concentration of antigen