Cell-Mediated Immunity Flashcards

1
Q

What are the two T-cell co-receptors and what type of effector cells do they give rise to?

A

1) CD4 - T-helper (TH1, TH2, TH17, TFH), T-regulatory
2) CD8 - Cytotoxic T-cells

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2
Q

T-cells recognize antigens only when ____

A

Presented by APCs on either MHC I or MHC II - creating a unique peptide-MHC complex recognized by that particular TCR

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3
Q

MHC is also known as ____.

A

HLA

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4
Q

All nucleated cells display MHC ____.

A

Class I

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5
Q

Professional APCs display MHC ____.

A

Class I and II

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6
Q

Differentiation of CD4+ T-cells into respective effector cells is driven by…

A

Cytokines

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7
Q

How are TH1 cells activated and what is their function?

A

Activated via IFN-γ and via CD40L binding CD40, they help activate macrophages to phagocytose

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8
Q

What is the function of TH2 cells?

A
  • Important in allergic pathways
  • They release cytokines to promote class switching of B cells to secrete IgE, and recruit mast cells and eosinophils
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9
Q

What is the function of TH17 cells?

A
  • Release cytokines that promote neutrophils and other phagocyte recruitment
  • Helpful for fungal infections
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10
Q

What is the function of TFH cells?

A

Bind to B cells to activate them, initiating humoral immunity (isotype switching, Ab production)

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11
Q

What is the function of Treg cells?

A

Help to suppress and regulate the immune response

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12
Q

How does immunotherapy work?

A

Causes a shift from TH2 pathway to TH1, helping to increase tolerance to allergens

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13
Q

Intravesicular pathogens may persist within phagolysosomes; these are killed via the ____ effector pathway.

A

TH1

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14
Q

How are peptides loaded onto MHC I?

A
  • After MHC I is assembled in the ER, viral proteins in the cytosol are cleaved by proteosomes and transferred to the ER, where they are loaded onto MHC I
  • Peptide-loaded MHC I then “buds” off ER and goes to cell surface where it will alert CD8+ T cells
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15
Q

Like B-cells, variable regions of the TCR are made via…

A

Somatic recombination (aka VDJ recombination)

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16
Q

What are TRECs?

A
  • T-cell receptor excision circles are the segments of DNA that are excised during VDJ recombination.
  • TRECS remain but do not replicate and are diluted over time
  • Measured in newborn screening; no TRECS = no T cells
17
Q

What is positive selection?

A

TCR must bind to self-MHC with some loose affinity to be selected; double positive thymocytes will then commit to either CD4 or CD8

18
Q

Where does self-MHC come from for T cell development in the thymus?

A

Thymic cortical epithelial cells

19
Q

What is negative selection?

A

If double-positive thymocytes bind too strongly to self-MHC, self-peptide complexes, they will undergo apoptosis (to avoid autoimmunity)

20
Q

What are the three requirements for T cell activation?

A

1) TCR has to bind to MHC-peptide complex
2) Co-stimulatory molecules between APC and T cell must bind
3) Cytokines from the APC must activate the T cell

21
Q

T cells both produce and require which cytokine for proliferation/division?

A

IL-2

22
Q

What are two mechanisms by which CTLs induce apoptosis?

A

1) FAS pathway - binding of CTL Fas ligand to Fas on target cell
2) Formation of pores via perforin and release of granzymes into pores

23
Q

The most common cause of CD4+ T cell deficiency is…

A

HIV