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近红外光免疫治疗:癌症治疗的最新进展及其靶分子综述。

Near Infrared Photoimmunotherapy: A Review of Recent Progress and Their Target Molecules for Cancer Therapy.

机构信息

Department of Gynecology and Obstetrics, Medical Faculty, Justus-Liebig-University Giessen, Klinikstr. 33, 35392 Giessen, Germany.

出版信息

Int J Mol Sci. 2023 Jan 31;24(3):2655. doi: 10.3390/ijms24032655.

Abstract

Near infrared photoimmunotherapy (NIR-PIT) is a newly developed molecular targeted cancer treatment, which selectively kills cancer cells or immune-regulatory cells and induces therapeutic host immune responses by administrating a cancer targeting moiety conjugated with IRdye700. The local exposure to near-infrared (NIR) light causes a photo-induced ligand release reaction, which causes damage to the target cell, resulting in immunogenic cell death (ICD) with little or no side effect to the surrounding normal cells. Moreover, NIR-PIT can generate an immune response in distant metastases and inhibit further cancer attack by combing cancer cells targeting NIR-PIT and immune regulatory cells targeting NIR-PIT or other cancer treatment modalities. Several recent improvements in NIR-PIT have been explored such as catheter-driven NIR light delivery, real-time monitoring of cancer, and the development of new target molecule, leading to NIR-PIT being considered as a promising cancer therapy. In this review, we discuss the progress of NIR-PIT, their mechanism and design strategies for cancer treatment. Furthermore, the overall possible targeting molecules for NIR-PIT with their application for cancer treatment are briefly summarised.

摘要

近红外光免疫治疗(NIR-PIT)是一种新开发的分子靶向癌症治疗方法,通过给予与 IRdye700 缀合的癌症靶向部分,选择性地杀死癌细胞或免疫调节细胞,并诱导治疗性宿主免疫反应。局部暴露于近红外(NIR)光会引起光诱导的配体释放反应,从而对靶细胞造成损伤,导致免疫原性细胞死亡(ICD),对周围正常细胞几乎没有或没有副作用。此外,NIR-PIT 可以通过结合针对 NIR-PIT 的癌细胞和针对 NIR-PIT 的免疫调节细胞或其他癌症治疗方式,在远处转移部位产生免疫反应并抑制进一步的癌症攻击。最近已经探索了一些 NIR-PIT 的改进,例如导管驱动的 NIR 光传递、癌症的实时监测以及新靶分子的开发,这使得 NIR-PIT 被认为是一种很有前途的癌症治疗方法。在这篇综述中,我们讨论了 NIR-PIT 的进展、它们的机制和用于癌症治疗的设计策略。此外,还简要总结了 NIR-PIT 的总体可能靶向分子及其在癌症治疗中的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/403f/9916513/042d2410337e/ijms-24-02655-g001.jpg

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