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Pseudomonas aeruginosa lipopolysaccharide (LPS) O11 is a complex glycolipid located in the outer membrane of the Gram-negative bacterium Pseudomonas aeruginosa, specifically defining the O11 serotype. It consists of a conserved lipid A moiety, a core oligosaccharide, and a highly variable O-specific polysaccharide (O-antigen) that extends into the extracellular environment (Pier, 2007, PubMed: 17510665). This molecule serves as a critical virulence factor by providing structural integrity to the cell wall and acting as a barrier against host immune components, including complement proteins and cationic antimicrobial peptides (King et al., 2009, PubMed: 19129407). The O11 serotype is one of the most prevalent strains isolated from patients with hospital-acquired infections, such as ventilator-associated pneumonia and bacteremia. Consequently, the O11-specific O-antigen is a primary target for passive immunotherapy and vaccine development. For example, Panobacumab (AR-101) is a human monoclonal IgM antibody designed to bind specifically to the O11 O-polysaccharide, thereby enhancing opsonophagocytic killing of the bacteria by host neutrophils (Horn et al., 2010, PubMed: 21135141). While highly effective against its specific serotype, the therapeutic use of such agents is limited by the high degree of antigenic variation among different P. aeruginosa strains.
Binding to the O-polysaccharide moiety of the lipopolysaccharide to facilitate opsonophagocytosis by host immune cells and neutralize endotoxic activity.
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