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Bio 328 Immunology

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Bio 328 Immunology Leukocyte migration and inflammation – PowerPoint PPT presentation

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Title: Bio 328 Immunology


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Bio 328 Immunology Leukocyte migration and
inflammation
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Innate or natural immunity.
  • Innate vs adaptive response
  • Passive Defenses
  • Mechanical properties boundaries
  • Chemical properties boundaries
  • Inflammatory response
  • Mobilization of active defenses
  • Initiation of innate responses
  • Effectors of the active, innate response
  • Soluble mediators
  • Cellular mediators

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  • Acute Inflammatory Response
  • Mobilization of active defenses
  • Vasodilation
  • Vascular permeability
  • Recruitment of neutrophils
  • Localized vs systemic.

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Tissue damage exposes the blood protein Factor
VII to Tissue Factor expressed on the basolateral
surface of endothelial cells.
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Kinin system
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C3bB
C3bBb
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Plasmin
Bradykinin
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PlasminogenActivatorinactive
Kallikrein Thrombin Elastase Cathepsin Plasmin
PlasminogenActivatoractive
C3 and C5
Plasminogen
Plasmin
C3a and C3bC5a and C5b
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C3 activation
MBL (mannose, fucose) Ficolins (N-aceylglucosamine
) C1q (LPS) CRP-phosphocholine)
Plasmin
kallikrein
Different ways to activate complement.
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Vasodilation and increased vascular permeability
lead to fluid leakage (edema) and extravasation
of neutrophils.
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  • Cellular component of inflammatory response
  • Neutrophils phagocytosis.
  • (resident) Macrophages and Dendritic cells
    augmentation of acute inflammatory response (and
    initiation of adaptive response).
  • Mast cells augmentation of inflammatory response.

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Lipoxygenase
Cyclooxygenase
Leukotrienes
Prostaglandins
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Inflammatory Response
Systemic Response Liver Hypothalamus Bone Marrow
Local Response Epithelial cells Endothelial
cells Macrophages/ Dendritic cells
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Endothelial cells Cytoskeleton E- and
P-Selectin ICAM-1/2 Interleukin-8 MHC-I
Macrophages/Dendritic cells IL-1, TNFa, IL-6 AA
metabolites iNos, Cox2 Interleukin-8 Defensins MHC
-I, MHC-II
Vasodilation Vasopermeability Recruitment
neutrophils
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C-reactive Protein A Pentraxin
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(Phosphocholine)
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Ligand-bound CRP recruits and binds C1q and
activates the classic pathway of
complement, Ligand-bound CRP is recognized by the
Fcg receptor and, thus, is an opsonin.
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  • Resolve the Inflammatory response
  • LPS tolerance short form of MyD88, protein
    phosphatases, sTNFaR and sIL-1R, IL-1Ra.
  • IL-10 and TGFb.
  • Decay-Activating Factor.
  • Arachidonic acid metabolites (Charles Serhan).

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Chronic inflammation persistent infections,
autoimmunity, tissue damage, obesity. Macrophages
and TH1 INFg and TNFa (cachectin) Fibrosis and
granuloma
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Chronic Inflammation accumulation and continuous
activation of macrophages.
Fibrosis Scar tissuefibroblast
proliferationcollagen production
Granuloma
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William Coley (1862-1936).
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Coleys toxin
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  • Anti-inflammatory therapy
  • Anti-adhesin therapy
  • Corticosteroids (prednisone, prednisolone, and
    methylprednisolone
  • NSAIDS (aspirine, Tylenol, ibuprofen, Naproxen)

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Celebrex, Vioxx
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CR3
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  • Extra-vasation cells squeeze between neighboring
    endothelial cells without interupting the
    integrity of the endothelium
  • Homotypic binding of PECAM-1 of the leukocyte
    with PECAM-1 of the tight junction of the
    endothelial cells.
  • LFA-1 binds to JAM-1 of the junctional complex
  • PECAM Platelet Endothelial Cell Adhesion
    Molecule.
  • JAM Junctional cell Adhesion Molecule.

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PSGL-1 P-selectin Glycoprotein Ligand-1
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aLb2 LFA-1) a4b1 (VLA-1)
CCL21 CCl19 T cells CXCL12
CXCL13 B cells
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Gut CCL25binds CCR9
CCL17CCL27CCL1
a4b7
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The End
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