“…CD14 is an APP, and several clinical studies have reported increased serum levels of sCD14 in a range of inflammatory conditions (Bas et al, 2004). Higher serum levels are associated with several insulin-resistance-related phenotypes (Fernandez-Real et al, 2003), systemic lupus erythematosus (Egerer et al, 2000), atopic dermatitis (Wuthrich et al, 1992), systemic inflammatory response syndrome (Stoiser et al, 1998), angina (Zalai et al, 2001), preterm labor even in the absence of infection (Gardella et al, 2001), multiple organ failure (Endo et al, 1994), rheumatoid arthritis (Horneff et al, 1993;Yu et al, 1998), multiple sclerosis (Lutterotti et al, 2006), Kawasaki disease (Takeshita et al, 2000), and Gaucher's disease (Hollak et al, 1997). These associations may reflect CD14's capacity to bind to nonmicrobial factors such as monosodium urate crystals (Scott et al, 2006), host heat shock proteins (Kol et al, 2000), integrins (Humphries & Humphries, 2007), surfactant proteins (Sano et al, 2000), atherogenic lipids, and lipoproteins (Schmitz & Orso, 2002), but they also suggest that sCD14 may modulate host immune responses to other ''danger'' signals besides those of microbial origin.…”