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光动力疗法治疗癌症后增强免疫反应的联合方法。

Combination approaches to potentiate immune response after photodynamic therapy for cancer.

机构信息

Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, MA 02114, USA.

出版信息

Photochem Photobiol Sci. 2011 May;10(5):792-801. doi: 10.1039/c0pp00326c. Epub 2011 Apr 9.

Abstract

Photodynamic therapy (PDT) has been used as a cancer therapy for forty years but has not advanced to a mainstream cancer treatment. Although it has been shown to be an efficient way to destroy local tumors by a combination of non-toxic dyes and harmless visible light, it is its additional effects in mediating the stimulation of the host immune system that gives PDT great potential to become more widely used. Although the stimulation of tumor-specific cytotoxic T-cells that can destroy distant tumor deposits after PDT has been reported in some animal models, it remains the exception rather than the rule. This realization has prompted several investigators to test various combination approaches that could potentiate the immune recognition of tumor antigens that have been released after PDT. This review will cover these combination approaches using immunostimulants including various microbial preparations that activate Toll-like receptors and other receptors for pathogen-associated molecular patterns, cytokines growth factors, and approaches that target regulatory T-cells. We believe that by understanding the methods employed by tumors to evade immune response and neutralizing them, more precise ways of potentiating PDT-induced immunity can be devised.

摘要

光动力疗法(PDT)已被用作癌症治疗达四十年,但并未发展成为主流癌症治疗方法。尽管已经证明它是一种通过非毒性染料和无害可见光相结合来有效破坏局部肿瘤的方法,但它在介导宿主免疫系统刺激方面的额外作用使 PDT 具有更大的潜力得到更广泛的应用。尽管在一些动物模型中已经报道了 PDT 后可以刺激能够破坏远处肿瘤沉积物的肿瘤特异性细胞毒性 T 细胞,但这仍然是例外而不是规则。这一认识促使一些研究人员测试各种组合方法,以增强对 PDT 后释放的肿瘤抗原的免疫识别。这篇综述将涵盖这些使用免疫刺激剂的组合方法,包括激活 Toll 样受体和其他病原体相关分子模式受体的各种微生物制剂,细胞因子和生长因子,以及针对调节性 T 细胞的方法。我们相信,通过了解肿瘤逃避免疫反应的方法并加以中和,就可以设计出更精确的增强 PDT 诱导免疫的方法。

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