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应用细小病毒 B19 样颗粒进行自发光光动力学疗法治疗实体瘤。

Use of parvovirus B19-like particles in self-illuminated photodynamic therapy for solid tumors.

机构信息

Departamento de Bioquímica, Facultad de Medicina, Universidad Nacional Autónoma de México (UNAM), México City 04510, Mexico.

Facultad de Estudios Superiores Iztacala, UNAM, Tlalnepantla de Baz, Estado de México 54090, Mexico.

出版信息

J Photochem Photobiol B. 2024 Sep;258:112979. doi: 10.1016/j.jphotobiol.2024.112979. Epub 2024 Jul 11.

DOI:10.1016/j.jphotobiol.2024.112979
PMID:39003970
Abstract

Bioluminescence resonance energy transfer photodynamic therapy, which uses light generated by bioluminescent proteins to activate photosensitizers and produce reactive oxygen species without the need for external irradiation, has shown promising results in cancer models. However, the characterization of delivery systems that can incorporate the components of this therapy for preferential delivery to the tumor remains necessary. In this work, we have characterized parvovirus B19-like particles (B19V-VLPs) as a platform for a photosensitizer and a bioluminescent protein. By chemical and biorthogonal conjugation, we conjugated rose Bengal photosensitizer and firefly luciferase to B19V-VLPs and a protein for added specificity. The results showed that B19V-VLPs can withstand decoration with all three components without affecting its structure or stability. The conjugated luciferase showed activity and was able to activate rose Bengal to produce singlet oxygen without the need for external light. The photodynamic reaction generated by the functionalized VLPs-B19 can decrease the viability of tumor cells in vitro and affect tumor growth and metastasis in the 4 T1 model. Treatment with functionalized VLPs-B19 also increased the percentage of CD4 and CD8 cell populations in the spleen and in inguinal lymph nodes compared to vehicle-treated mice. Our results support B19V-VLPs as a delivery platform for bioluminescent photodynamic therapy components to solid tumors.

摘要

生物发光共振能量转移光动力疗法利用生物发光蛋白产生的光来激活光敏剂并产生活性氧,而无需外部照射,在癌症模型中显示出有希望的结果。然而,仍然需要对能够将这种治疗的成分进行优先递送至肿瘤的输送系统进行表征。在这项工作中,我们将细小病毒 B19 样颗粒(B19V-VLPs)作为光敏剂和生物发光蛋白的平台进行了表征。通过化学和生物正交偶联,我们将孟加拉玫瑰红光敏剂和萤火虫荧光素酶与 B19V-VLPs 和一种增加特异性的蛋白偶联。结果表明,B19V-VLPs 可以承受所有三种成分的修饰而不会影响其结构或稳定性。共轭的荧光素酶具有活性,并且能够在不需要外部光的情况下激活孟加拉玫瑰红产生单线态氧。功能化 VLPs-B19 产生的光动力反应可以降低体外肿瘤细胞的活力,并影响 4T1 模型中的肿瘤生长和转移。与载体处理的小鼠相比,用功能化 VLPs-B19 处理还增加了脾脏和腹股沟淋巴结中 CD4 和 CD8 细胞群体的百分比。我们的结果支持 B19V-VLPs 作为生物发光光动力治疗成分向实体瘤的输送平台。

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