Date published: 2025-9-17

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CD14 Inhibitors

CD14 is a glycoprotein primarily expressed on the surface of macrophages and monocytes, as well as certain dendritic cells. It plays a pivotal role in the innate immune system, functioning as a pattern recognition receptor (PRR) that recognizes pathogen-associated molecular patterns (PAMPs), such as lipopolysaccharide (LPS) from Gram-negative bacteria. The primary function of CD14 is to facilitate the recognition and binding of these microbial molecules, thereby initiating immune responses against invading pathogens. Upon binding to PAMPs, CD14 activates downstream signaling pathways that lead to the production of pro-inflammatory cytokines and chemokines, as well as the upregulation of co-stimulatory molecules, ultimately promoting the clearance of pathogens and the initiation of adaptive immune responses. Inhibition of CD14 can be achieved through various mechanisms, all of which aim to disrupt its interaction with PAMPs and subsequent activation of immune responses. One approach to inhibiting CD14 function is through the use of competitive inhibitors that block the binding site of CD14, preventing its interaction with PAMPs. Another strategy involves interfering with downstream signaling pathways activated by CD14, thereby inhibiting the production of inflammatory mediators. Additionally, modulating the expression or activity of CD14 itself can also be employed as a means of inhibition. By targeting CD14, it is possible to attenuate excessive immune responses and inflammation associated with various infectious and inflammatory diseases.

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