Gardner Madison, Turner Jeffrey E, Youssef Osama A, Cheshier Samuel
Neurosurgery, University of Utah, Salt Lake City, USA.
Neurosurgery, Huntsman Cancer Institute, Salt Lake City, USA.
Cureus. 2020 Oct 15;12(10):e10964. doi: 10.7759/cureus.10964.
Tumor-associated macrophages (TAMs) have recently emerged as potentially crucial therapeutic targets for cancer. Thus, the development of macrophage-mediated phagocytosis assays is vital for preclinical drug screening of different tumor cells. This assay can be used to evaluate the effect of anti-cancer therapy, such as immunotherapy, radiotherapy, and chemotherapy, on different tumor cells. Here, we describe the in-vitro phagocytosis assay in detail. As an example of immunotherapy treatment, we used a monoclonal antibody to block an anti-phagocytic signal (CD47) to evaluate the assay using human brain tumor cells and monocyte-derived macrophages. We also demonstrated that this assay can be used to evaluate the effect of different irradiation doses on the phagocytosis of brain tumor cells. This functional assay is fast, accurate, and highly reproducible. Furthermore, the results successfully demonstrate that anti-CD47 antibodies and irradiation can enhance the macrophage-mediated phagocytosis of brain tumors.
肿瘤相关巨噬细胞(TAMs)最近已成为癌症潜在的关键治疗靶点。因此,巨噬细胞介导的吞噬试验的开发对于不同肿瘤细胞的临床前药物筛选至关重要。该试验可用于评估免疫疗法、放射疗法和化学疗法等抗癌治疗对不同肿瘤细胞的效果。在此,我们详细描述体外吞噬试验。作为免疫疗法治疗的一个例子,我们使用单克隆抗体阻断抗吞噬信号(CD47),以用人脑肿瘤细胞和单核细胞衍生的巨噬细胞评估该试验。我们还证明该试验可用于评估不同辐射剂量对脑肿瘤细胞吞噬作用的影响。这种功能试验快速、准确且高度可重复。此外,结果成功证明抗CD47抗体和辐射可增强巨噬细胞介导的脑肿瘤吞噬作用。