Title: Bio 328 Immunology
1Bio 328 Immunology Leukocyte migration and
inflammation
2Innate 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
3- Acute Inflammatory Response
- Mobilization of active defenses
- Vasodilation
- Vascular permeability
- Recruitment of neutrophils
- Localized vs systemic.
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7Tissue damage exposes the blood protein Factor
VII to Tissue Factor expressed on the basolateral
surface of endothelial cells.
8Kinin system
9C3bB
C3bBb
10Plasmin
Bradykinin
11PlasminogenActivatorinactive
Kallikrein Thrombin Elastase Cathepsin Plasmin
PlasminogenActivatoractive
C3 and C5
Plasminogen
Plasmin
C3a and C3bC5a and C5b
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13C3 activation
MBL (mannose, fucose) Ficolins (N-aceylglucosamine
) C1q (LPS) CRP-phosphocholine)
Plasmin
kallikrein
Different ways to activate complement.
14Vasodilation and increased vascular permeability
lead to fluid leakage (edema) and extravasation
of neutrophils.
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17- 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.
18Lipoxygenase
Cyclooxygenase
Leukotrienes
Prostaglandins
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20Inflammatory Response
Systemic Response Liver Hypothalamus Bone Marrow
Local Response Epithelial cells Endothelial
cells Macrophages/ Dendritic cells
21Endothelial 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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30C-reactive Protein A Pentraxin
31(Phosphocholine)
32Ligand-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.
33- 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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36Chronic inflammation persistent infections,
autoimmunity, tissue damage, obesity. Macrophages
and TH1 INFg and TNFa (cachectin) Fibrosis and
granuloma
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39Chronic Inflammation accumulation and continuous
activation of macrophages.
Fibrosis Scar tissuefibroblast
proliferationcollagen production
Granuloma
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41William Coley (1862-1936).
42Coleys toxin
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46- Anti-inflammatory therapy
- Anti-adhesin therapy
- Corticosteroids (prednisone, prednisolone, and
methylprednisolone - NSAIDS (aspirine, Tylenol, ibuprofen, Naproxen)
47Celebrex, Vioxx
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54CR3
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63- 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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65PSGL-1 P-selectin Glycoprotein Ligand-1
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72aLb2 LFA-1) a4b1 (VLA-1)
CCL21 CCl19 T cells CXCL12
CXCL13 B cells
73Gut CCL25binds CCR9
CCL17CCL27CCL1
a4b7
74The End