RESUMEN
Sepsis is a systemic host response to invasive infection by bacteria. Despite treatment with antibiotics, current mortality rates are in the range of 20%-25%, which makes sepsis the most important cause of death in intensive care. Gram-negative bacteria are a prominent cause of sepsis. Lipopolysaccharide (LPS), one of the major constituents of the outer membrane of Gram-negative bacteria, plays a major role in activating the host's immune response by binding to monocytes and other cells. Several proteins are involved in neutralization and clearance of LPS from the bloodstream. Here, we provide evidence that ß2-glycoprotein I (ß2GPI) is a scavenger of LPS. In vitro, ß2GPI inhibited LPS-induced expression of tissue factor and IL-6 from monocytes and endothelial cells. Binding of ß2GPI to LPS caused a conformational change in ß2GPI that led to binding of the ß2GPI-LPS complex to monocytes and ultimately clearance of this complex. Furthermore, plasma levels of ß2GPI were inversely correlated with temperature rise and the response of inflammatory markers after a bolus injection of LPS in healthy individuals. Together, these observations provide evidence that ß2GPI is involved in the neutralization and clearance of LPS and identify ß2GPI as a component of innate immunity.