在胰腺癌中,抗bag3治疗对肿瘤相关巨噬细胞的消耗是对PD-1阻断的补充

Yi Sun, R. Torphy, Yuwen Zhu
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引用次数: 0

摘要

发表在Gut杂志上的新文献表明,联合使用抗BAG3单抗和抗pd -1单抗治疗胰腺癌可以消除肿瘤相关巨噬细胞(tam),增加肿瘤浸润CD8+ T细胞,并导致肿瘤生长抑制(1)。这些发现突出了BAG3 (bcl -2相关的thanogene 3)作为治疗靶点与免疫检查点阻断联合治疗胰腺癌的潜力。
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Depletion of tumor associated macrophages by anti-BAG3 treatment complements PD-1 blockade in pancreatic cancer
New literature published in Gut has shown that combined treatment of anti-BAG3 mAb and anti-PD-1 mAb in pancreatic cancer can eliminate tumor-associated macrophages (TAMs), increase tumor infiltrating CD8+ T cells and result in tumor growth suppression (1). These findings highlight the potential of BAG3 (Bcl-2-associated athanogene 3) as a therapeutic target in conjunction with immune checkpoint blockade in the treatment of pancreatic cancer.
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