Unit 2 Flashcards

1
Q

When only 1 type of TCR or BCR is transcribed per cell.

Ex. 1 Heavy chain and light chain allele is transcribed/ B cell. 1 B and 1 a chain allele is transcribed / T cell.

A

Allelic Exclusion

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2
Q

When does isotype switching occur? How does it occur?

A

When: After antigen is met, in the lymph node. The release of chemokines causes IgM or IgD to become IgG, IgA or IgE.
How: AID targets “switch regions” and removes them. This is regulated by cytokines

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3
Q

When the constant region of antibody switches but not the variable region.

A

isotype switching

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4
Q

Cytokines for isotype switching:

  1. IL-4
  2. TGF-B
  3. IL-5
  4. IFN-y
A
  1. IgG1, IgE
  2. IGA, IgG2b
  3. IgA
  4. IgG3, IgG2a
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5
Q

When antigen binds to pAPC and activates a B or T cell, causing proliferation.

A

clonal selection

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6
Q

many genes

A

polygeny

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7
Q

many alleles of same gene

A

polymorphism

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8
Q

exogeous pathway for MHC surface expression proteins

A

invariant chain, CLIP, HLA-DM

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9
Q

endogenous pathway for MHC surface expression proteins

A

Immunoproteosome, TAP transporter, ER

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10
Q

How does cross presentation work?

A

Antigens engulfed by a protein gets placed into pathway for MHC Class I.

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11
Q

T Cell Development: Process

A
  1. T cell precursor in the thymus 2. B forms and proliferates (somatic recombination). 3. good B are selected (surrogate a chain is added and goes to the surface. If it binds well to CD3, B works) 4. a is formed. 5. DP (CD8 and CD4 forms) 6. Can either become a T reg, death by neglect, or bind to cortical endo cells with MHC class I or II. 7. SP cells go to medulla. 8. If not bind to MTECS, go to tissues for activation. If bind, either anergy, apoptosis, or receptor editing.
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12
Q

B Cell Development: Process

A
  1. pre-pro B cell in bone marrow. 2. Heavy chain is recombined. Surrogate L chain binds and goes to cell surface and proliferates. 3. Light chain forms. 4. If binds to self antigens in bone marrow–> apoptosis or receptor editing. 4. Goes to spleen T1 (produces a lot of IgM). 5. T2 reaches follice and starts producing igD. 6. B-2 cells produce both and goes to activation.
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13
Q

When B cells are self reactive in bone marrow

A

Central Tolerance

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14
Q

When self reactive B cells are killed

A

Clonal Deletion

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15
Q

T Cell activation (helper)

A
  1. TCR binds to antigen on MHC class II. 2 Costimulatory molecules on pAPCS bind. 3. cytokines.
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16
Q

Cytokine signalling for T Cell Differentation

  1. IL-2, TGF-B
  2. IL-1, IL-6, IL-23, TGF-B
  3. IL-4
  4. IL-6, IL-21
  5. IL-12, IFN-y, IL-18
A
  1. T cell produces IL-10, TGF-B–> T reg
  2. IL-17A,IL-17 B, IL-22–>Th17 cell (protects fungal and bacterial, inflammation)
  3. IL-4, IL-5, IL-13–>Th2 cell (allergy and anti-helminth)
  4. IL-4, IL-21–>Tfh(helps B cells in follicles and germinal center in spleen)
  5. IFN-y, TNF–>Th1(enhances cytotoxic T cell activation, APC activity, intracellular pathogen)
17
Q

What consists of central SMAC

A

TCR/CD3, CD4/CD8, CD28 on T Cell–CD80/86 on APC

18
Q

What consists of peripheral SMAC

A

LFA-1 (T) –ICAM-1 (APC), CD2(T)–IFA-3(APC)

19
Q

Which type of cells are present class I and classII MHC

A

class I is present in all nucleated cells, class II in pAPCs.

20
Q

Gene for MHC

A

II (DP, DQ,DR), III (C4, C2, BF), I (BCA)

21
Q

What is the name of the transcription factor that picks random genomes and adds them to medulla epithelial cells in thymus?

A

AIRE

22
Q

Costimulators can be negative or positive

A

Immunomodulation