Reddan J C, Anderson C Y, Xu H, Hrabovsky S, Freye K, Fairchild R, Tubesing K A, Elmets C A
Department of Otolaryngology, Case Western Reserve University, University Hospitals of Cleveland, OH, USA.
Photochem Photobiol. 1999 Jul;70(1):72-7.
The purpose of this study was to determine if silicon phthalocyanine 4 (Pc 4), a second-generation photosensitizer being evaluated for the photodynamic therapy (PDT) of solid tumors, was immunosuppressive. Mice treated with Pc 4 PDT 3 days before dinitrofluorobenzene sensitization showed significant suppression of their cell-mediated immune response when compared to mice that were not exposed to PDT. The response was dose dependent, required both Pc 4 and light and occurred at a skin site remote from that exposed to the laser. The immunosuppression could not be reversed by in vivo pre-treatment of mice with antibodies to tumor necrosis factor-alpha or interleukin-10. These results provide evidence that induction of cell-mediated immunity is suppressed after Pc 4 PDT. Strategies that prevent PDT-mediated immunosuppression may therefore enhance the efficacy of this therapeutic modality.
本研究的目的是确定第二代用于实体瘤光动力疗法(PDT)评估的光敏剂硅酞菁4(Pc 4)是否具有免疫抑制作用。与未接受光动力疗法的小鼠相比,在二硝基氟苯致敏前3天接受Pc 4光动力疗法治疗的小鼠,其细胞介导的免疫反应受到显著抑制。该反应呈剂量依赖性,需要Pc 4和光照两者,且发生在远离激光照射部位的皮肤部位。用抗肿瘤坏死因子-α或白细胞介素-10抗体对小鼠进行体内预处理并不能逆转免疫抑制作用。这些结果提供了证据,表明Pc 4光动力疗法后细胞介导的免疫诱导受到抑制。因此,预防光动力疗法介导的免疫抑制的策略可能会提高这种治疗方式的疗效。