Department of Integrative Oncology, BC Cancer Research Centre, British Columbia Cancer Agency, Vancouver, BC, Canada.
Department of Biochemistry and Molecular Biology, Medical University of South Carolina, Charleston, SC, USA.
Methods Mol Biol. 2022;2451:569-577. doi: 10.1007/978-1-0716-2099-1_28.
Recently, it has become clear that a prerequisite requirement for most cancer therapies is controlling the negative impact of the activity of immunosuppressory cell populations. It is therefore of a considerable interest to develop treatments for containing the operation of major myeloid and lymphoid immunoregulatory cell populations. We have reported that acid ceramidase inhibitor LCL521 effectively overrides the activity of immunoregulatory T cells (Tregs) and myeloid-derived suppressor cells (MDSCs) engaged in the context of tumor response to photodynamic therapy (PDT). The present communication dissects and describes in detail the procedure for the use of LCL521 as an adjuvant to PDT for improved cure rates of treated tumors based on restricting the activity of immunoregulatory cell populations.
最近,人们已经清楚地认识到,大多数癌症疗法的一个先决条件要求是控制免疫抑制细胞群活性的负面影响。因此,开发控制主要髓样和淋巴样免疫调节细胞群功能的治疗方法具有相当大的意义。我们已经报告称,酸性神经酰胺酶抑制剂 LCL521 可以有效地克服参与光动力疗法(PDT)治疗肿瘤反应的免疫调节 T 细胞(Tregs)和髓样来源的抑制细胞(MDSCs)的活性。本通讯详细剖析并描述了将 LCL521 用作 PDT 的辅助剂以提高治疗肿瘤的治愈率的过程,该过程基于限制免疫调节细胞群的活性。