Lecture 22: Cell mediated immunity and lymphocyte ontogeny Flashcards

1
Q

Whats the significance of % serum antibody vs antibody affinity graphs?

A
  • With polyclonal antibodies antibody affinity is a bell shaped curve against % of serum antibody i.e theres a range of affinities and epitopes produced.
  • Monoclonal antibodies are created by selecting a single epitope and single affinity (immortalise by fusing ab-forming cells with B cell tumour cells(myeloma))
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2
Q

In B-Chronic Lymphocytic Leukemia what is the chemotherapy regime?

A

If aggressive, RFC chemotherapy

R- Rituximab (Anti-CD20 Mab)
F- Fludarabine (Purine analog, inhibits cell replicaton)
C- Cyclophosphamide (Alkylating agent, anti-mitotic)

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3
Q

In non-HLA matched transplants whats the difference between the first and second graft rejection?

A

First graft - Day 12, mostly T cell mediated destruction

Second graft - Day 5, Mostly antibody mediated

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4
Q

Of the millions of T cells, how many epitopes do they recognise?

A

Each t cell recognizes one epitope with their TcR

CD8 T cell + (APC + Class 1 HLA) requires Thelper cytokines leading to proliferation and differentiation

= Cytotoxic T cells and memory cells

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5
Q

What are the three killing mechanisms of CD8 T cells?

A

1) Perforin + Enzymes for polymerization
2) Hydrolytic enzymes
= Digestive enzyme through pores

3) Cytokines, TNFa, IFNg
= Induced apoptosis

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6
Q

What is the origin of lymphocyte precursors?

A
  • Thymus ( T cells)
  • Bone marrow (B cells)

and they migrate to secondary lymphoid organs to mature

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7
Q

Describe B cell ontogeny?

A

In the bone marrow:

  • Uncommitted stem cells have no antigen specificity
  • These develop into Pre-B-cells (Here heavy chains re-arrange genes to commit to antibody type)
  • Immature B cells (have surface IgM)(Re-arranges light chains to match heavy)

Leaves bone marrow as mature B cells containing surface IgM and IgD (Express both, committed to one shape)

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8
Q

Describe the rearrangement of genes in relation to heavy and light chains:

A

Light genes: One constant exon, & One variable region is randomly selected and AA removed, added when bound

Heavy genes: Five constant heavy chain exons, Only one VDJ are selected, making hypervariability)

Re-arrangement determines antigen specificity

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9
Q

Describe central tolerance in relation to B cells:

A
  • Uncommitted stem cells
  • Pre-B-Cell
  • Immature B cell -> Gets exposed to self antigen, if strongly reactive then clonal deletion occurs.
  • But not all antigens are expressed in thymus so peripheral tolerance is T cell mediated and they dont give cofactors if not appropriate.
  • Mature B cell (Surface IgM and IgD)
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10
Q

Describe class switching:

A

Class switching - Removes constant regions by T cell signaling, altering type of immunoglobulin but same specificity.

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11
Q

What are the important points of B cell ontogeny and immunoglobulin genes?

A
  • Development in bone marrow
  • Multiple VDJ exons recombine = V-region
  • Recombination independent of antigen
  • Variable region diversity arises from this
  • B cells become committed to one V(H) and one V(L)
  • Single constant region exons for each class
  • Negative selection to remove strong self reactivity
  • Class switching retains V-region, changes c-region

Implications
= V,D,J exons important in determining antibody repertoire
= Class switching retains specificity but alters antibody functions

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12
Q

The thymus shrinks with age, whats the implication of this?

A

Fewer new T cells later in life

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13
Q

Describe thymus structure:

A

Insert slide 24

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14
Q

Describe T cell ontogeny:

A
  • Uncommitted thymocyte -> TCR gene rearrange
  • TCR has both CD4 and CD8, No HLA recognition at all = death (Positive selection)
  • HLA recognition is stronger for either CD4 or CD8 and that determines its lineage. (Other CD is down regulated)
  • These are exposed to Anti-self HLA + Self peptide, reactivity = negative selection and death.

Those cells that dont react to self peptide survive and are exported to secondary lymphoid organs

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15
Q

Whats the important points of T cell ontogeny and T cell receptor genes?

A
  • Development in thymus
  • Multiple VDJ exons recombine = V region
  • Recombinant independent of antigen
  • T cells become comimitted to one Valpha and Vbeta
  • Positive seleciton for HLA class one or two recognition (Requires CD4 or CD8)
  • Negative selection against strong self-reactivity

Implications

  • V, D, J exons important in determining repertoire
  • HLA influences T cell receptor repertoire
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