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Pathogenic bacteria, their components, and toxins represent a broad class of molecules and organisms that cause infectious diseases in humans; therapeutic targeting can be achieved at various levels, including whole bacterial cells (via antibiotics or phages), specific cell wall/membrane proteins, secreted toxins (neutralized by monoclonal antibodies), or metabolic and virulence pathways essential for bacterial survival and pathogenicity. These targets are highly diverse and include both whole organisms and a spectrum of molecules unique to pathogens, such as bacterial enzymes, toxins, and structural components. Because of this diversity, specificity and safety of therapies vary, and bacterial resistance is an ongoing clinical challenge[1][2][3][4].
Inhibition of cell wall or protein/nucleic acid synthesis; Neutralization of bacterial toxins (by monoclonal antibodies); Disruption of membrane or metabolic pathways; Bacteriolysis (by phages or lytic antibiotics); Inhibition of virulence factors (e.g., secretion system, biofilm formation)
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