pathoma Flashcards
Complement classical pathway
C1 binds IgG or IgG bound to antigen
Hageman factor (FXII)
inactive proinflammatory protein produced in liver; important in DIC (esp GN sepsis); activates coagulation/fibrinolytic system, complement, and kinin system
Kinin system
Cleaves HMWK into bradykinin, which vasodilates and increases vascular permeability, and mediate pain
Pain mediated by
PGE2, bradykinin sensitize nerves
PMN migration factors
LTB4, C5a, IL-8, and bacterial products
Redness, warmth MOA
Vasodilation of arteriolar smooth muscle, mediated by histamine, prostaglandin (PGI2, D2, E2), and bradykinin
Swelling mediated by
Histamine, tissue damage
Fever mediated by
Pyrogens (e.g. LPS) release IL-1 and TNF, which travel to brian and increase COase activity in perivascular cells of the hypothalamus; and increase PGE2, which raises temp set point
Chemotactic for PMN
C5a
Opsonin for phagocytosis
IgG, C3b
Anaphylatoxin
C3a, C5a
In acute inflammation, fluid and cells enter where?
Post-capillary venule
What slows PMN in blood vessels?
Selectins (“rolling”): E selectin (TNF, IL-1); P selectin (Weibel Palade bodies, mediated by histamine)
Weibel Palde bodies has what two factors?
VWF, P-selectin
Selectins bind what on leukocytes?
Sialyl Lewis X
E-selectin, CAMs on endothelium induced by
TNF and IL-1
Integrins on leukocytes induced by
C5a, LTB4 (same ones that brought PMN to the area)
LAD defect of integrins
CD18 subunit
Chediak-Higashi syndrome
Microtubule defect leads to impaired phagolysosome formation
Anti-inflammatory cytokines
IL-10, TGF-beta
Defining characteristic of granulomatous inflammation
Epithelial histiocytes (surrounded by giant cells, rim of lymphocytes)
DiGeorge syndrome
Development failure of 3rd, 4th pharyngeal pouch; 22q11 microdeletion
Sjogren three main criteria
Dry eyes, anti-ribonucleoprotein antibodies, and lymphocyticsialadenitis
Labile tissue
Bowel, skin, BM
Stable tissue
Liver
Permanent tissue
Myocardium, skeletal muscle, and neurons