Lecture 20- Adaptive Immunity 2 Flashcards

1
Q

What do ATC’s do when activated with antigen?

A

Travel to lymph node

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2
Q

Where in lymph node are b and T cells

A

B cells in lymphoid follicle

T cells in parafollicular cortex

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3
Q

Whatcauses autoimmune disease?

A

When cells act against self antigen

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4
Q

Where are b and T cells produced and where do they mature?

A

Produced in bone marrow

T cells mature in thymus and B cells in tissues

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5
Q

Why do lymph nodes swell during infection?

A

Lymphadenopathy- B cells and T cells become activated

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6
Q

What happens with activation of CD4+ T cells also known as T helper cells?

A

They go on to help B cells produce antibodies

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7
Q

Clinically important lymph nodes?

A

Cervical
Axillary
Inguinal

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8
Q

Antibody response?

A

Bacteria

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9
Q

Effector T cell cytotoxic response?

A

If virus

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10
Q

Antigen recognition by T lymphocytes?

A

Antigen recognition receptor (t cell receptor TCR)

Great diversity to recognise different antigens

CD4+ helper T cells recognise MHC class 2 while CD8+ recognise MHC class 1

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11
Q

How are T cells activated on recognition of an antigen?

A

3 signals

Antigens presented by MHC 1 or 2

Cytokines released

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12
Q

Effect of cytokines on activation of CD4+ cells?

A

Cytokines released depends on type of microbe and cause different sub types of CD4+ cell to arise

can get TH1 cells responsible for cell mediated immunity (intracellular and extracellular pathogens)

TH1 help B cells produce antibodies

Th2 cells responsible for humoral immunity (extracellular pathogens)

TH17 causes neutrophil recruitment and activation

Treg causes immune suppression

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13
Q

What happens if there is a virus in an APC?

A

APC,s have class 1 and 2 MHC molecules so will activate CD4+ and CD8+ cells

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14
Q

Effector functions of CD8+ cells?

A

Require TH1 cells to become activated and have cytotoxic function

Naive CD8+ cells can either become cytotoxic in activation as above or memory CD8 cells

Cytotoxic will kill all MHC class 1 cells

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15
Q

B cell antigen recognition?

A

Do not need antigens to be processed

Endocytosis and present through MHC class 2 to helper T cells

Get antibody and cytokine production

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16
Q

Outcome of B lymphocyte activation?

A

IgM production which is T helper independent

IgG, IgE and IgA which is T helper dependent. This is why IgM is seen first.

Disease can be detected at lower concentration in future

Memory B cells for long lasting immunity

17
Q

What can antigen stimulated B cells become?

A

Plasma cells which produce IgM and are T cell or thymus independent

Other cell types which are thymus dependent and produce the other antibodies

Memory B cells

18
Q

Relevance of IgM and IgG clinically?

A

If high IgM and no IgG then first time exposure to antigen.

If IgG present then secondary exposure and immunity should be there

19
Q

Effector functions of antibodies?

A

IgG- complement activation, can give vertical immunity for 6 months to offspring (autoimmune risk)

IgE- good against parasites

IgA- mucosal immunity

IgM-complement activation