Hunt D W, Chan A H
QLT PhotoTherapeutics Inc, Vancouver, British Columbia, V5Z 4H5, Canada.
IDrugs. 1999 Mar;2(3):231-6.
Photodynamic therapy (PDT) is widely recognized as a technique with which to treat malignant tumors that are accessible to an activating light source. PDT utilizes light absorbing compounds that catalyse the formation of cytotoxic oxygen species to produce the antitumor effect subsequent to direct light irradiation. PDT also exhibits immunomodulatory attributes. The photodynamic treatment of solid tumors triggers a large influx of granulocytes and macrophages into the region, leading to T-cell mediated anti tumor immunity against residual cancer. In apparent contrast, the application of levels of light less than those required for tumor ablation and over a larger body surface lessened disease severity when applied in murine autoimmune models. Furthermore, PDT is inhibitory for immunologically-mediated reactions to topically applied chemical haptens. The capacity of PDT to influence immune responses appears related to its capacity to target activated T lymphocytes as well as influence the immunostimulatory attributes of antigen presenting cells.
光动力疗法(PDT)被广泛认为是一种治疗可被激活光源照射到的恶性肿瘤的技术。PDT利用光吸收化合物,在直接光照后催化细胞毒性氧物种的形成,从而产生抗肿瘤作用。PDT还具有免疫调节特性。实体瘤的光动力治疗会引发大量粒细胞和巨噬细胞涌入该区域,导致T细胞介导的针对残留癌症的抗肿瘤免疫。明显相反的是,在小鼠自身免疫模型中应用低于肿瘤消融所需强度且覆盖更大体表面积的光照时,疾病严重程度会降低。此外,PDT对局部应用化学半抗原的免疫介导反应具有抑制作用。PDT影响免疫反应的能力似乎与其靶向活化T淋巴细胞以及影响抗原呈递细胞免疫刺激特性的能力有关。