16 - Immunological Memory Flashcards

1
Q

Linked recognition

A

T cells and B cells must recognise antigens contained within the same molecular complex in order to interact

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2
Q

Immunological memory

A
  • Does not require repeated exposure to original antigen
  • Memory cells may be sustained by cytokines produced in response to infection with other, unrelated pathogens
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3
Q

Naive T cells in lymph nodes

A

Naive T cells activated in the T cell rich area of lymph node by DC become follicular T helper cells, express CXCR5 and move towards B cell zone where they attach to activated B cells via linked recognition

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4
Q

Primary focus

A
  • Formation takes about 5 days
  • B cells activated in the primary foci move to adjacent follicles to become germinal centre (GC) B cells, or the medullary cords of LN to become plasma cells in situ
  • Surviving GC B cells that have undergone class switching and affinity maturation will become either high affinity memory B cells or long lived plasma cells
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5
Q

Plasma cells in situ

A

Secrete antibody for a few days, then undergo apoptosis

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6
Q

high affinity memory B cells/long lived plasma cells

A

Become resident in bone marrow where they continue to secrete antibodies into the blood for months - years

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7
Q

Memory B cells

A
  • Divide very slowly
  • Express surface Ig but do not secrete antibody
  • May differentiate into plasma cells, allowing long term production of antibody
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8
Q

Repeated immunisation

A

Leads to increasing affinity of antibody due to somatic hypermutation and selection by antigen in germinal centers

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9
Q

Memory B cells during secondary exposure

A

During secondary exposure to antigen, antibodies persisting from primary immune response immediately bind to pathogen to initiate phagocytosis and complement pathway

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10
Q

Primary response

A
  • Following activation of naive cells
  • Consists of antibodies derived from diverse population of precursor B cells specific for different epitopes
  • Low affinity with few somatic mutations
  • Isotype is IgM class switching to IgG
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11
Q

Secondary response

A
  • Mediated by memory cells
  • Derived from high affinity B cells which have undergone significant clonal expansion
  • High affinity antibodies with extensive somatic mutation
  • Isotype is IgG and IgA
  • More intense and effective response
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12
Q

How do naive T cells home to lymph nodes

A

Through binding of L selectin (CD62L) to sulphated carbohydrates (e.g. CD34) displayed on surface of HEV

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13
Q

How can naive T cells be identified

A

CD45RA

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14
Q

How can effector T cells be identified

A

CD45RO

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15
Q

Receptors expressed on the surface of effector T cells and their ligands

A
  • Lose expression of L selectin
  • Express LFA-1 which binds to ICAM-1
  • Express VLA-4 which binds to VCAM-1
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16
Q

Signals required for T cell survival

A

Restimulation with IL-7, IL-15 and with self antigens presented by MHC

17
Q

what do naive T cell differentiate into

A

Effector T cell or memory T cell

18
Q

Why are elderly more susceptible to infection

A
  • Capacity to produce naive cells is lost with age, must rely on memory cells
  • Problem when new strain arises
19
Q

Memory T cells

A
  • TCR does not undergo class switching or somatic hypermutation
  • Identified via expression of cell surface molecules
20
Q

Marker of T cell activation

A

CD69

21
Q

Marker of activated T cell

A

CD44

22
Q

Two types of memory cells that CD4 and CD8 cells differentiate into

A
  • Effector memory cells (Tem)
  • Central memory cells (Tcm)
23
Q

Effector memory cells (Tem)

A
  • Rapidly differentiate into effector T cells after restimulation, and secrete large amounts of IFN-gamma, IL-4, IL-5
  • Lack chemokine receptor CCR7
  • Express high levels of integrins such as LFA-1
  • Specialised for rapidly entering inflamed tissues
24
Q

CCR7

A

(required for entry of naive T cells into HEV, therefore Tem cells are excluded from lymph nodes

25
Q

Central memory T cells (Tcm)

A
  • Express CCR7 and can enter lymphoid tissue, as do naive T cells
  • On stimulation with antigen, rapidly lose expression of CCR7 and differentiate into Tem cells
26
Q

Further differentiation of Tem cells

A

Further differentiate into Th1 or Th2 cells, determining the cytokines these cells produce

27
Q

CD4 T cells

A
  • Promote the maintenance of CD8 memory cells
  • In absence of MHC class 2 proteins, CD4 T cells fail to develop in thymus
28
Q

Tissue resident memory (TRM) T cells

A
  • Major immune compartment that surveys peripheral tissues for reinfection
  • Activated CD8 and CD4 T cells enter dermis and other peripheral tissues (via CXCR3)
  • induction of CD69 expression on T cells leads to their retention in dermis
29
Q

Original antigenic sin

A

When individuals who have been infected with one variant of influenza virus are infected with a second or third variant, they make antibodies only against epitopes that were present on the initial virus

30
Q

Tools for measuring antigen specific T cells

A
  • Tetramers are reagents used in flow cytometry to identify and track antigen specific T cells
  • The combination of MHC class 1 and antigen peptide must be known (synthesised)
  • This MHC/peptide complex is labeled with a fluorophore, and added to the T cells being analysed
  • Attachments of the tetramer to a T cell indicates the presence of an antigen specific T cell
  • Detection of other markers (e.g. CD45RO) indicates effector or memory phenotypes