Immunological memory Flashcards

1
Q

where are short-lived plasma cells located?

A

They reside in the lymph node or spleen

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2
Q

where are long-lived plasma cells located?

A

They reside in the bone marrow where they receive survival signals from stromal cells

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3
Q

what is the function of long-lived plasma cells?

A

They are a source of long-lasting high-affinity class-switch antibody

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4
Q

what are plasma cells?

A

Antibody factories

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5
Q

where do memory B cells come from?

A

they arise from the germinal centre reaction

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6
Q

what are the features of memory B cells?

A

they have inherited the genetic changes from the germinal centre reaction
- express high-affinity antibody
- have undergone antibody class switching

They express higher levels of MHC II and co-stimulatory molecules than naive B cells

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7
Q

where are memory B cells found?

A

They populate the spleen and lymph nodes and circulate through the blood

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8
Q

how do memory B cells express antibody?

A

Express surface Ig but do not secrete antobody

  • Quickly generate antibody producing plasma cells when they re-encounter antigen
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9
Q

what do most vaccines rely on?

A

B cell memory

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10
Q

what are memory T cells?

A

long-libed cells that survive after the contraction of the effector phase

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11
Q

what is needed for survival of memory T cells?

A

IL-7 and IL-15
- memory T cells also need to contact self-peptide:self MHC complexes to continue to proliferate (does not need to be specfic antigen)

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12
Q

what are the features of memory T cells?

A

-Higher precursor frequency
- Different activation requirements and cell surface proteins from naive and effector cells

  • Memory T cells divide more frequently than naive T cells
  • Memory pool size is dictated by a balance between cell proliferation and cell death
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13
Q

what do memory T cells need to be effective?

A
  • know where to go
  • Be able to get there quickly or already be there
  • Have good fighter equipment
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14
Q

what are the differences between memory T cells and effector T cells?

A
  • They proliferate more than naive T cells and to a lower level of antigen dose
  • Require less co-stimulation for activation than naive cells
  • Produce cytokine faster and retain their polarised phenotype
  • May be strategically positioned in the tissue where the pathogen is likely to be encountered
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15
Q

what are the features of central memory?

A

-Express lymph-node homing molecules
- Slower than effector memory cells to produce cytkine

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16
Q

what are the features of effector memory?

A

-lack lymph-node homing molecule expression
- rapidly produce cytokine upon antigenic stimulation

17
Q

what are lymph noe homing molecules and where are they expressed?

A

Lymph node homing molecules CCR7 and CD62L are co-expressed on a subset of CD4 and CD8 memory T cells in human peripheral blood

18
Q

what are Tcm and Tem cell subsets?

A

Tcm is CCR7+ (not very good at making cytokine)
Tem is CCR7-

19
Q

what is the difference between Tcm and Tem cell subsets?

A

Tem persist in tissue and are functionally superior to Tcm
- discovery that after viral or bacterial infection memory CD8 T cells moved to non-lymphoid tissues and remained as long-lived memory cells. These cells were more lytic than memory CD8 T cells from the spleen

20
Q

what are the features of tissue resident memory?

A

-Lack lymph-node homing molecule expression, express the integrin CD103 and CD69. Do not recirculate in the blood.
- Rapidly produce cytokine upon antigenic stimulation

21
Q

how where Trm T cells discovered?

A

Discovery that after infection memory CD8+ T cells can remain in tissues after infection has cleared without recirculating in the blood

22
Q

where do you not find resident memory T cells?

A

in the blood

23
Q

what is the linear model of memory T cell development?

A

Memory cells develop directly from differentiated effector cells

24
Q

what is the evidence that supports the linear model of memory T cell development?

A

Adoptive transfer studies show adoptively transferred effect CD4 and CD8 T cells develop into memory populations that retain similar functional polarisation to the effect cells

25
Q

what is the progressive model of memory T cell development?

A

The degree of activation dictates the fate of a cell

26
Q

what evidence supports the progressive model of memory T cell development?

A

transcriptional profile analysis of naive, memory, and effector CD8 T cells generated after vaccination, suggest cumulative antigen stimulation drives naive T cells to differentiate into memory T cells, then into terminally differentiated effector T cells

27
Q

what is the divergent model of memory T cell development?

A

T cells are destined to an effector or memory lineage due to asymmetric cell division

28
Q

what supports the divergent model of memory T cell development?

A

clustering of receptors and molecules at the immunological synapse causes uneven distribution of cell contents in daughter cells

29
Q

what is innate immune ‘memory’?

A

Epigenetic changes in monocytes result in a long-lasting enhanced protection against infection

30
Q

what is the evidence for innate immune ‘memory’?

A

many vaccines have effects that extend beyond the targeted disease