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Explore how neutrophils shape the immune response in health and disease. This poster highlights neutrophil pathogen defense mechanisms, including phagocytosis, degranulation, and NETosis, as well as neutrophil roles in inflammation and NET-associated pathologies.
DOWNLOAD NOWOzenoxacin is a quinolone antibiotic.1 It is active against clinical isolates of S. pyogenes, P aeruginosa, and P. acnes and clinical isolates of antibiotic-sensitive and -resistant S. aureus, S. epidermidis, and S. pneumoniae (MIC50s = 0.00625-1.56 mg/L). Ozenoxacin inhibits S. aureus DNA gyrase and topoisomerase IV (IC50s = 4.5 and 0.617 mg/L, respectively). It reduces insulin- or 5α-dihydroxy testosterone-induced triglyceride production and lipid droplet formation in primary hamster sebocytes when used at a concentration of 30 µM.2 Ozenoxacin (30 µg/ml) decreases heat-killed C. acnes-induced increases in IL-6 and IL-8 production in HEKa primary human keratinocytes and IL-1β, IL-6, IL-8, and TNF-α production in THP-1 monocytes.3 Topical application of ozenoxacin (1%) decreases skin lesion bacterial counts in a mouse model of burn infection caused by S. aureus.1 Formulations containing ozenoxacin have been used in the treatment of S. aureus- or S. pyogenes-associated impetigo.
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1. In vitro and in vivo antibacterial activity of T-
2. Ozenoxacin suppresses sebum production by inhibiting mTORC1 activation in differentiated hamster sebocytes. J. Dermatol. 51(9), 1187-1198 (2024).
3. Anti-