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光动力疗法治疗肿瘤的免疫机制研究进展
引用本文:薛欢,王佩茹,王秀丽.光动力疗法治疗肿瘤的免疫机制研究进展[J].国际免疫学杂志,2020(1):51-55.
作者姓名:薛欢  王佩茹  王秀丽
作者单位:安徽医科大学上海皮肤病临床学院;同济大学医学院光医学研究所上海市皮肤病医院
基金项目:国家自然科学基金(81872212,81872512);上海市浦江人才计划(17PJ1408500);中央高校基本科研业务费专项资金资助(221201800101);上海市卫生计生系统优青计划(2017YQ066)。
摘    要:光动力疗法(photodynamic therapy,PDT)是治疗肿瘤的有效手段之一,PDT治疗可导致肿瘤细胞的死亡和凋亡,并损伤肿瘤相关血管.近年来,PDT的免疫机制越来越受到关注.肿瘤细胞的免疫逃逸是肿瘤发生发展的重要因素.PDT治疗肿瘤时,可通过免疫原性细胞死亡(immunogenic cell death,ICD)诱导肿瘤细胞表达损伤相关分子模式(damage associated molecular patterns,DAMPs),从而活化树突状细胞,诱导机体特异性抗肿瘤免疫.同时,PDT还可影响肿瘤微环境中的相关免疫细胞和因子,进而增强机体抗肿瘤反应.光动力治疗和其他免疫治疗联合应用亦能增强疗效.故光动力治疗的免疫机制研究将为肿瘤治疗提供可能的新思路.

关 键 词:光动力疗法  免疫原性细胞死亡  损伤相关分子模式  肿瘤微环境

Advances in research on immune mechanism of photodynamic therapy for tumor
Xue Huan,Wang Peiru,Wang Xiuli.Advances in research on immune mechanism of photodynamic therapy for tumor[J].International Journal of Immunology,2020(1):51-55.
Authors:Xue Huan  Wang Peiru  Wang Xiuli
Institution:(Shanghai Skin Disease Clinical College of Anhui Medical University,Shanghai 200443,China;Institute of Photomedicine,Shanghai Skin Disease Hospital,Tongji University School of Medicine,Shanghai 200443,China)
Abstract:Photodynamic therapy(PDT)is an effective method for the treatment of cutaneous carcinoma,which can cause tumor cell death and apoptosis,and damage tumor-associated blood vessels.In recent years,the immune mechanism of PDT has also received attention.The tumor immune escape in tumorigenesis is an important factor.PDT therapy can induce tumor cells to express damage associated molecular patterns(DAMPs)by immunogenic cell death(ICD),thereby activating dendritic cells(DCs)and inducing anti-tumor adaptive immune responses.At the same time,PDT can affect the relevant immune cells and factors in the tumor microenvironment(TME),thus enhancing the body′s anti-tumor response.The combination of photodynamic therapy and other immunotherapies can also enhance efficacy.Therefore,the research on the immune mechanism of photodynamic therapy will provide possible new ideas for cancer treatment.
Keywords:Photodynamic therapy  Immunogenic cell death  Damage associated molecular patterns  Tumor microenvironment
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