Lecture 13 Flashcards

1
Q

Describe Dendritic Licensing. What is it used for and what is activated first? Go through the rest of the process.

A

To reach full capacity of CD8+ proliferation DC has to first activate CD4+ cells

Once CD4 cell is activated will express CD40L and concurrently release IFNy

Upregulation of CD80/86 on DC [amplifies cross-presentation]

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2
Q

What are the four steps for the activation of a CD8+ T Cell? Are cytokine signals vita for CD8+ activation?

A
  1. DC migrate to the central part of the HEV (population of naïve T cells)
  2. Through cross-presentation will present the Ag to naïve CD8+ T cell
    - Phagolysosome leakage of viral particles
    - Presentation via MHC I [MHC II presentation is concurrent]
  3. Requires co-stimulation: CD80/86 (DC)- CD28 (T-cell)
  4. THIRD signal (cytokines) is not vital here
    - Peripheral IL-2: required for expansion of CD8+ cells
    - CD8+ cells alone do not produce sufficient amounts of IL12
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3
Q

What are the 3 functions of CD8+ T Cells?

Hint: Releases 2 chemicals and has 1 function.

A

Cytokines (IFNy and TNFalpha)
Chemoattractants (MIP 1 alpha/beta), RANTES
Lysis of infected cells (perforins, granzymes, Fas/Fas/L)

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4
Q

How do you activate CTL Cytotoxic Killing?

A

Immunological Synapse Formation

-TCR-MHC I on target cell

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5
Q

What are the two ways CTL kills?

A

Release of perforin (homolog to C9) and Granzymes (Granzyme B activates caspase 3)

Fas/FasL mediated killing

  • External pathway [Type 1] verses internal pathway [Type 2]
  • DNA degradation final result
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6
Q

What is a very bad possibility that can occur with chronic stimulation of CTL? What specifically does this cause?

A

Exhaustion of T-cells

-In chronic infection, downregulation of IFNy and increased expression of PD-1 (inhibitory receptor)

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7
Q

What cell produces IL2 the most? What does this cause?

A

CD4+

It has an autocrine loop to positively produce more IL2

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8
Q

What cells produce IL15? What 2 things does this cause?

A

Produced by macrophage resident cells and DC and can aid in proliferation

  • Chemoattractant for T cell migration
  • Way to cause CTL proliferation in periphery
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9
Q

What cells produce IFNy? What are the 4 effector functions of IFNy?

A

Produced by NK cells, CD4+ cells and CD8+ cells themselves and help with differentiation of CD8+ into effector CTL

  • Increased MHC class I expression makes the environment more sensitive to recognition by CD8+ cells
  • Potent activator of macrophage resident cells
  • B cell differentiation (IgG)
  • Th1 differentiation (Note that also IL12 does this)
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10
Q

What cells produce IL12? What are the 3 functions of IL12?

A

Produced by macrophage resident cells and DCs

  • Prevents CD8+ T cell exhaustion
  • Th1 differentiation
  • Activates NK cells
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11
Q

What produces IL21? What does it help aid in the differentiation of?

A

produced by activated CD4+ cells (activated) and aid in CD8+ memory T cells

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12
Q

Do NKT cells have to differenetiate to have effector function? What part of immunity do they contribute to?

A

No

They are part of the innate immunity and are the first line of defense

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13
Q

How do you activate NKT cells?

A

Activated upon recognition of lipids presented through CD1d [MHC like protein]

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14
Q

What cytokines does NKT cells release? What do they play a part in given the cytokines they release?

A

Release cytokines: IL10, TGF-beta, Th1 and Th2 cytokines

-Play a role in T-cell differentiation

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15
Q

What happens as a result of the overactivation of T cells?

What are 2 types of diseases that are associated with this occuring?

A

Overactivation of NKT cells will produce effects similar to uncontrolled regulation of T-cells
-Allergy, Autoimmune diseases (Atherosclerosis)

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16
Q

What are the 2 direct ways NKT cells kill?

A
  1. NKT cells kills tumor cell [GzmB/FasL]

2. NKT concurrently releases IFNy release triggers resident NK cells to perform anti-tumor activities

17
Q

What are the 3 indirect ways NKT cells kill?

A
  1. NKT cell recognizes CD1d on resident APC or TAM (tissue-associated macrophage resident cell) and kills [GzmB/FasL]
  2. Creates a less immunosuppressive environment
  3. Concurrent IFNy release triggers resident NK cell to perform anti-tumor activity
    • But NOW easier to infiltrate tumor