Pizova Klara, Tomankova Katerina, Daskova Adela, Binder Svatopluk, Bajgar Robert, Kolarova Hana
Department of Medical Biophysics, Faculty of Medicine and Dentistry and Institute of Molecular and Translational Medicine, Palacky University Olomouc, Czech Republic.
Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2012 Jun;156(2):93-102. doi: 10.5507/bp.2012.056.
Photodynamic therapy (PDT) is a new modality in cancer treatment. It is based on the tumour-selective accumulation of a photosensitizer followed by irradiation with light of a specific wavelength. PDT is becoming widely accepted owing to its relative specificity and selectivity along with absence of the harmful side-effects of chemo and radiotherapy. There are three known distinct mechanisms of tumour destruction following PDT, generation of reactive oxygen species which can directly kill tumour cells, tumour vascular shutdown which can independently lead to tumour destruction via lack of oxygen and nutrients and thirdly enhanced antitumour immunity.
A review based on the literature acquired from the PubMed database from 1983 with a focus on the enhanced antitumour immunity effects of PTD.
Tumour cell death is accompanied by the release of a large number of inflammatory mediators. These induce a non-specific inflammatory response followed by gradual adaptive antitumour immunity. Further, a combination of PDT with the immunological approach has the potential to improve PDT efficiency and increase the cure rate. This short review covers specific methods for achieving these goals.
光动力疗法(PDT)是癌症治疗中的一种新方法。它基于光敏剂在肿瘤中的选择性积聚,随后用特定波长的光进行照射。由于其相对特异性和选择性,以及不存在化疗和放疗的有害副作用,PDT正被广泛接受。PDT后肿瘤破坏有三种已知的不同机制,即产生活性氧可直接杀死肿瘤细胞、肿瘤血管关闭可通过缺氧和营养缺乏独立导致肿瘤破坏,以及增强抗肿瘤免疫力。
基于从1983年PubMed数据库获取的文献进行综述,重点关注PTD的增强抗肿瘤免疫效应。
肿瘤细胞死亡伴随着大量炎症介质的释放。这些介质诱导非特异性炎症反应,随后逐渐产生适应性抗肿瘤免疫。此外,PDT与免疫方法相结合有可能提高PDT效率并提高治愈率。这篇简短的综述涵盖了实现这些目标的具体方法。