Immunology 5 - B lymphocytes Flashcards

1
Q

What is an epitope?

A

The site on an antigen where an antibody binds

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2
Q

Where do B cells originate from?

A

Derived from stem cells in the bone marrow

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3
Q

How are mature B cells specific?

A

They have different B cell receptors

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4
Q

Describe the process of clonal selection

A
  • Each lymphocyte bears a single, unique receptor
  • Interaction between a foreign molecule and that receptor leads to activation
  • Differentiated effector cells of that lineage will bear the same receptor
  • Self specific receptors are deleted early in development
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5
Q

Describe the structure and distribution of the B Cell Receptors.

A
  • Consists of Iga and Igb subunits.
  • mIg is present - tail is too sort to signal
  • Iga and Igb tails are long enough to interact with intracellular signalling molecules
  • Is present in thousands of identical copies on the surface of the B lymphocyte
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6
Q

How is antibody receptor diversity generated?

A
  • Each BCR receptor chain) is encoded by separate multigene families on different chromosomes, which are rearranged and bought together.
  • They are rearranged by splicing.
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7
Q

How are segments joined in generation of antibodies?

A

During joining of gene segments unused DNA is looped out and removed by Rag/recombinase genes. Lack of Rag1 / Rag2 results in scid

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8
Q

Describe the stages of B cell development

A

Pro B cells (early to late) -> Pre B cells (large to small) -> naive B cells (immature to mature)

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9
Q

How are naive B cells activated?

A
  • Naive B cells cannot be activated by binding to the antigen alone.
  • An accessory signal is required (either directly from microbial constituents or from a T helper cell)
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10
Q

What is the difference between the two pathways of antibody production of B cells?

A
  • T helper cells (thymus dependent) involves all Ig classes and has memory
  • Microbial constituents (thymus independent) only uses IgM and has no memory
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11
Q

How does thymus independent activation of B cells occur?

A
  • B cell receptors bind to bacterial components/polysaccharide as it must be a repetitive structure
  • Second signal is provided by the microbial constituent or an accessory cell.
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12
Q

How does thymus dependent activation of B cells occur?

A
  • The membrane bound BCR recognises antigen
  • The receptor-bound antigen is internalised and degraded into peptides
  • Peptides associate with self molecules and are expressed at the cell surface
  • This complex is recognised by matched CD4 T helper cell
  • B cell activated to express cytokine receptors, which T cell derived cytokines bind to causing the B cells to proliferate and differentiate
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13
Q

What is the consequence of thymus dependent activation of B cells?

A
  • T helper cells secrete lymphokines to direct the immune system
  • B cells form plasma cells (secrete soluble BCRs/antibodies) and memory cells
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14
Q

What is the Ig class switch?

A
  • T cells release cytokines which cause the DNA of the B cell to change, and this results in production of the heavy chain
  • This changes the class of the antibody - IgM/IgD to IgG/IgA/IgE
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15
Q

How does immunological memory form in relation to B cellsand wat is the purpose?

A
  • Occurs following clonal selection/once the immune system has recognised and responded to an antigen
  • Antigen-specific lymphocytes (B + T) are the cellular basis
  • Memory responses are characterised by a more rapid and heightened immune reaction that serves to eliminate pathogens fast and prevent diseases.
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16
Q

What classifications of antibody are used in the primary and secondary response?

A

Primary - IgM at the beginning, IgG later.

Secondary - Small amount of IgM, large amount of IgG from the start

17
Q

When are B cells bad?

A
  • Autoimmune conditions
  • Allergy (IgE in anahylaxis)
  • B cells to myelomas/lymphomas
18
Q

Describe the processes of somatic hypermutation and affinity maturation

A
  • Between the primary and secondary immune response, the antibodies and B cells used are optomised
  • AID converts C to U (makes C-G pair to A-T in DNA) resulting in small mutations that could be beneficial or not
  • Antibodies that bind well will surivive for to improve the immune response
  • Occurs in the lymph node