Innate immunity and antigen presentation Flashcards

1
Q

Brief definition innate immunity

A

Physical barrier to infectious agents, such as microbicidal factors in body fluids (lysozyme, complement) and phagocytic cells.
Involve acute phase proteins

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2
Q

Phagocytosis summary

A

Adherence, membrane activation, phagosome formation, fusion and digestion and release of degraded products

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3
Q

What is phagocytosis promoted by?

A
  • PAMPS: Pathogen associated molecuar patterns, receptors for common bacterial cell wall components. weak interactions.
  • Receptors for C3b complement component (complement mediated opsonisation)
  • Receptors for Fc region of antibodies (immune complex mediated opsonisation)
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4
Q

What are the three types of PAMPS

They act as ligands that neutrophils recognise, and also that cells like dendritic cells recognise and release danger signals to immune system

A

Common cell wall structures: Lipopolysaccharides, peptidoglycans (mannans, mannoproteins

Bacterial metabolic products: N-formylmethioine peptides

Heat shock proteins: released by stressed cells

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5
Q

Acute phase proteins: Release, action

A

Release: Plasma proteins produced due to a danger signal from a dendritic cell for example IL-1. produced in the liver.

Act to promote tissue repair and resolution and limit damage. Enhance host resistance

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6
Q

Complement generalised?

A

First complement components bind to common cell wall components.’
Set off enzymatic set of reactions, activating furhter complement components that: Increase vascular permeability, chemotaxis of neutrophils and opsonisation (C3b)

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7
Q

Primary and secondary lymphoid organs

A

Primary: Bone marrow and Thymus (T cells originate in bone marrow and mature in thymus)
Secondary: Lymph nodes (tissue), spleen (blood), accessory lymphoid tissue (mucosal surfaces)

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8
Q

Cells of adaptive immune system
Lymphocyte: Effectors and regulators

Effectors: ____ production ( B cells); ____ ____ _____ (CD8 T lymphocytes); NK cells; ____ ____- ____ _____, ADCC, K cells.
Last two functions of same subset of cells

Regulators: ____ production (CD4 Tcells): ____ (viruses, bacteria, intracellular agents); ____ (parasites, allergies, multicellular); ____( regulatory T cells, down regulation); ____ (mucosa and inflammation)

A

Effectors: Antibody production ( B cells); antigen specific cytotoxicity (CD8 T lymphocytes); NK cells; antibody dependent cellular cytotoxicity, ADCC, K cells.
Last two functions of same subset of cells

Regulators: Cytokine production (CD4 Tcells): TH1 (viruses, bacteria, intracellular agents); TH2 (parasites, allergies, multicellular); Treg( regulatory T cells, down regulation); TH17 (mucosa and inflammation)

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9
Q

Antigen transport and presentation

  • Multiplying ____ in infection site e.g ___. _____ cells uptake ____, release ____ _____ also. Are ____
  • Transport through the _____ to _____ nodes, and rest in _____ region
  • Present _____ to _____ that travel through/into the ____
  • _____ specific cells are recruited
A
  • Multiplying bacteria in infection site e.g skin. Langerhans cells uptake antigens, release danger signals also. Are APC’s
  • Transport through the lymphatics to lymph nodes, and rest in paracortical region
  • Present antigens to lymphocytes that travel through/into the node
  • Antigen specific cells are recruited
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10
Q

APC functions

A
Antigen collection and transport
Antigen concentration
Antigen processing
Antigen presentation to lymphocytes
Co-stimulation of lymphocytes: by surface molecules or pro-inflammatory cytokines
Tolerance induction
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11
Q

Exogenous pathway of antigen presentation

A

Dendritic cells

Antigenic material is phagocytosed (fused with protease), and combined with a Class II MHC such as HLA DP, DQ or DR. Then expressed on the cell surface membrane

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12
Q

Endogenous pathway of antigen presentation

A

Inside any nucleated cell of our body

Viral infection, or altered gene expression by tumour cell?
New proteins made and broken down by proteosomes.
Some breakdown products on Class I MHC HLA A, B and C through TAP complex then MHC I to surface

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13
Q

Exogenous pathway versus Endogenous

A

Exogenous: peptides derived form ingested material; only specialised APC’s (dendritic,, B cells), presented by MHC II.

Endogenous: Peptides derived from cytoplasmic proteins, normal metabolism( viral peptides, modified self peptides (tumours), presented by MHC I

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