Immunology Processes Flashcards

1
Q

How are B cells made and where are they activated?

A

Hematopoietic stem cells in the bone marrow differentiate into a pro B cell, then a large pre B cell, then a small pre B cell, and then an IgM B cell, forming the BCR via VDJ recombination
-these migrate through the blood to secondary lymphoid organs to be activated

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2
Q

How are B cells activated?

A

Foreign antigens bind the BCR on the B cell. The B cells present this on MCHII to a helper T cell. It receives co-stimulation like CD40 and cytokines from the helper T cell. This causes the B cell to proliferate and promotes the formation of germinal centers and long-lived plasma and memory B cells. The type of cytokine determines antibody type

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3
Q

What is the immune response in the lymph nodes?

A
  • Antigen and APC from tissue travels into lymph node through afferent lymphatic channels.
  • Antigens processed by resident dendritic cells in the paracortex
  • Resident dendritic cells present antigen on MCHII to CD4 T helper cells, activating them
  • B cells activated by T helper cell or antigen directly
  • Activated B and T cells form primary follicles, which leads to the production of secondary follicles with germinal centres
  • Plasma B cells secrete antibodies which leave through efferent lymphatic vessels
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4
Q

What is the immune response in the spleen?

A
  • Foreign antigens are carried to the spleen from the splenic artery
  • Dendritic cells captures the antigens in the marginal zone, and move to the PALS along with T cells from the splenic artery
  • In the PALS dendritic cells activate helper T cells
  • Active helper T cells activate B cells which form secondary follicles with a germinal centre
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5
Q

How are long-lived plasma B cells or memory B cells formed?

A
  • A naive B cell moves into the dark zone of a germinal centre
  • In the dark zone it recieves costimulatory signal from CD4 helper T cells, causing them to undergo proliferation and somatic hypermutation
  • They are then selected for survival in the light zone. B cells with unfavourable BCR mutations are killed by apoptosis. B cells with favourable BCR mutations move further into the light zone
  • Here they receive a second survival signal from T helper cells and differentiate into either plasma or memory B cells
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6
Q

How are T cells activated and how are memory T cells produced?

A
  • Naive T cell is activated by a dendritic cell that presents an antigen to it
  • Naive T cells then differentiate into effector cells
  • Most effector T cells die by apoptosis after a few days, but some recieve survival signals from cytokines like IL-7 and/or IL-15
  • Forms a central memory T cell that has CCR7 and remain in lymphoid tissue
  • Forms an effector memory T cell that dosent have CCR7 and lives in tissues
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7
Q

What is the immune response in the gut?

A
  • The gut contains peyer’s patches which contain a pocket of clusters of B cells, T cells, dendritic cells, macrophages and germinal centres
  • An antigen is sampled and transported into the pocket by microfold cells using transcytosis
  • The antigen is taken up by dendritic cells, which then leads to the activation of T and B cells in the lamina propria
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8
Q

How do cytotoxic T cells become activated and exert its function on a virus?

A
  • Infected cells present present viral antigens on MHCI
  • Infected cells upregulate the fas receptor on its surface
  • Dendritic cells present viral antigens on MCHI via cross presentation
  • Cytotoxic T cell binds via its TCR and CD8 coreceptor and become activated
  • Fas ligand on cytotoxic T cell is upregulated and binds to fas on the infected cell triggering apoptosis of the infected cell
  • The cytotoxic T cell releases perforin and granzyme to trigger apoptosis of the infected cell
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