Matsumoto Ryu, Tanoue Kiyonori, Nakayama Chieri, Okawa Masashi, Hozaka Yuto, Idichi Tetsuya, Mataki Yuko, Ohtsuka Takao
Department of Digestive Surgery, Graduate School of Medical and Dental Sciences, Kagoshima University, Kagoshima 890-8520, Japan.
Shin Nippon Biomedical Laboratories, Miyanoura-cho, Kagoshima 891-1305, Japan.
Cancers (Basel). 2025 Sep 22;17(18):3090. doi: 10.3390/cancers17183090.
Pancreatic ductal adenocarcinoma (PDAC) is a critical disease requiring the development of novel effective therapeutic approaches due to its increasing global incidence and associated low survival rates. While immunotherapy, including immune checkpoint inhibitors, has shown efficacy against various tumors, developing an effective treatment approach for PDAC poses a challenge. This is primarily attributed to the complex and distinctive immune evasion mechanisms of PDAC. Recent studies have revealed that tumor-associated macrophages (TAMs) play a crucial role in enhancing immune evasion in PDAC. This role is mediated through multiple pathways, including cytokine secretion and the activation or suppression of diverse immune cells. A clear understanding of how macrophages contribute to PDAC proliferation could lead to the development of novel immune therapy approaches targeting TAMs. In this review, we summarized the multifaceted activities and roles of TAMs in PDAC and explored the potential effect of immunotherapeutic approaches on PDAC, with a particular focus on chimeric antigen receptor (CAR) macrophages. This review was based on promising findings from recent studies on CAR macrophage-based immunotherapy for solid tumors.
胰腺导管腺癌(PDAC)是一种严重的疾病,由于其在全球范围内的发病率不断上升以及相关的低生存率,需要开发新的有效治疗方法。虽然包括免疫检查点抑制剂在内的免疫疗法已显示出对各种肿瘤的疗效,但开发针对PDAC的有效治疗方法仍面临挑战。这主要归因于PDAC复杂且独特的免疫逃逸机制。最近的研究表明,肿瘤相关巨噬细胞(TAM)在增强PDAC的免疫逃逸中起关键作用。这一作用是通过多种途径介导的,包括细胞因子分泌以及对多种免疫细胞的激活或抑制。清楚了解巨噬细胞如何促进PDAC增殖可能会导致开发针对TAM的新型免疫治疗方法。在本综述中,我们总结了TAM在PDAC中的多方面活动和作用,并探讨了免疫治疗方法对PDAC的潜在影响,特别关注嵌合抗原受体(CAR)巨噬细胞。本综述基于最近关于基于CAR巨噬细胞的实体瘤免疫治疗的有前景的研究结果。