Department of Immunology, Tumor Immunology Group, Leiden University Medical Center, Leiden, The Netherlands.
Methods Mol Biol. 2022;2451:579-588. doi: 10.1007/978-1-0716-2099-1_29.
The field of photodynamic therapy (PDT) of cancer, like oncology research in general, is showing increasing interest in tumor immunology and immune effects of tumor treatment. Tumor ablation by PDT can lead to strong shifts in the composition of the immune cell infiltrate of tumors, and systemic effects of local therapy have been described. T lymphocytes, also known as T cells, are a type of adaptive immune cells that are of particular interest as they are very efficient in target cell recognition and killing, both at the treatment site and systemically. Moreover, T cells can constitute immunological memory to provide long-term protection. Several studies have described in detail how T-cell immune responses are induced by PDT and can play an important role in the therapeutic effect. This chapter describes several approaches of the analysis of T-cell responses during or after PDT in a mouse tumor model.
癌症的光动力疗法(PDT)领域,与一般的肿瘤学研究一样,对肿瘤免疫学和肿瘤治疗的免疫效应越来越感兴趣。PDT 消融肿瘤可导致肿瘤浸润免疫细胞组成发生强烈转变,并且已经描述了局部治疗的全身效应。T 淋巴细胞,也称为 T 细胞,是一种适应性免疫细胞,由于其在治疗部位和全身范围内对靶细胞的识别和杀伤非常有效,因此特别受到关注。此外,T 细胞可以构成免疫记忆,提供长期保护。有几项研究详细描述了 PDT 如何诱导 T 细胞免疫反应,并能在治疗效果中发挥重要作用。本章描述了在小鼠肿瘤模型中分析 PDT 期间或之后 T 细胞反应的几种方法。