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Anti-IL-8 monoclonal antibodies are a class of biologic therapies designed to neutralize Interleukin-8 (CXCL8), a pro-inflammatory chemokine that plays a multifaceted role in the tumor microenvironment (TME). IL-8 is a potent chemoattractant for neutrophils and myeloid-derived suppressor cells (MDSCs), which contribute to an immunosuppressive TME and facilitate tumor evasion from the immune system. Furthermore, IL-8 signaling promotes angiogenesis, epithelial-mesenchymal transition (EMT), and the maintenance of cancer stem cells. By binding to and neutralizing IL-8, these monoclonal antibodies aim to disrupt these pro-tumorigenic processes and enhance the activity of other immunotherapies, such as PD-1/PD-L1 inhibitors. Key clinical-stage candidates include BMS-986253 (formerly HuMax-IL8), developed by Bristol Myers Squibb, and AMY109, developed by Chugai Pharmaceutical. These agents are primarily being evaluated in Phase 1 and Phase 2 clinical trials for the treatment of advanced or metastatic solid tumors, including chordoma, colorectal cancer, and pancreatic cancer.
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