5. Adaptive Immunity Flashcards

1
Q

What are some features of APC’s?

A
  1. Strategically located at portals of entry - skin, mucous membranes, lymphoid organs, circulation
  2. Pathogen capture
  3. Diversity in PRR - can recognise intracellular and extracellular pathogens
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2
Q

What 3 processes must happen before an APC can present to a T cell?

A

Capture
Processing
Presentation

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3
Q

Which cells are APC’s?

A

Dendrititic cells (lymph nodes)
Langerhan’s cells (Skin)
Macrophages
B cells

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4
Q

How do APC’s recognise pathogens?

A

PAMPs on microbial surface bind to PRR’s on APC surface

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5
Q

What response is activated if an intracellular pathogen is detected?

A

Cell-dependent immunity:

  • Cytotoxic T cells
  • Antibodies
  • Macrophages
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6
Q

What response is activated if an extracellular pathogen is detected?

A

Humoral immunity:

  • Antibodies
  • Complement
  • Phagocytes
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7
Q

What determines the APC response generated?

A

The PAMP signal detected - if intracellular PAMP then it must be viral, so cell dependent response generated

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8
Q

Where are MHCI found?

A

All nucleated cells

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9
Q

What HLA types are MHCI?

A

HLA-A
HLA-B
HLA-C

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10
Q

Where are MHC II found?

A

APC’s (not they also express MHCI)

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11
Q

What HLA types are MHC II?

A

HLA-DQ
HLA-DR
HLA-DP

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12
Q

How do MHC molecules express diversity?

A

Co-dominant expression of both parental genes

Polymorphic genes- different alleles in each individual

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13
Q

How does the function of MHCI and II differ?

A

MHCI - present peptides from intracellular microbes

MHCII - present peptides from extracellular microbes

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14
Q

Which cells recognise MHCI?

A

CD8+ T cells

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15
Q

Which cells recognise MHCII?

A

CD4+ T cells

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16
Q

Outline the endogenous pathway leading to MHCI presentation?

A

Virus invades host cell
Proteosome splices viral proteins in peptide fragments which enter the ER via TAP proteins.
If there is the right MHCI, it will bind and be transported o the cell surface.

17
Q

Outline the exogenous pathway leading to MHCII presentation?

A

Pathogen is engulfed by pinocytosis into an endosome.
Endosome fuses with MHCII containing vesicle secreted by the ER.
MHCII-peptide complex is presented on the surface.

18
Q

How can MHC molecules lead to clinical problems?

A
  1. Organ transplant rejection if HLA mis-match

2. Auto-immune disease

19
Q

What receptor binds to MHC molecules?

A

T cell receptor

20
Q

Why will patients lacking CD4+ T cells also lack CD8+ cytotoxic lymphocytes?

A

CD4+ release cytokines which are needed to cause activation of CD8+ T cells

21
Q

Why will patients lacking in CD4+ T cells also lack IgG?

A

Release IFN gamma which stimulates isotope switching from IgM to IgG.

22
Q

What is the benefit of the secondary immune response?

A
Faster
Stronger
Longer duration
Higher Affinity
IgG antibody more efficient
23
Q

What is the function of IgA?

A

Mucosal immunity

Breast milk

24
Q

What is the function of IgM?

A

Complement activation

25
Q

What is the function of IgG?

A
  • Fc dependent phagocytosis
  • Complement activation
  • Neonatal immunity - placental transfer
  • Toxin/virus neutralisation
26
Q

What is the function of IgE?

A

Immunity against helminths

Mast cell degranulation in allergies

27
Q

What 3 costimulatory signals are required to activate a T cell?

A
  1. MHCII and TCR binding
  2. CD80/86 and CD28 binding
  3. Cytokines
28
Q

Which cells express CD28?

A

Naive T cells