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用于靶向CD8及乳腺癌中细胞毒性T细胞体内成像的短波红外发射纳米探针

Shortwave-Infrared-Emitting Nanoprobes for CD8 Targeting and In Vivo Imaging of Cytotoxic T Cells in Breast Cancer.

作者信息

Shah Jay V, Siebert Jake N, Zhao Xinyu, He Shuqing, Riman Richard E, Tan Mei Chee, Pierce Mark C, Lattime Edmund C, Ganapathy Vidya, Moghe Prabhas V

机构信息

Department of Biomedical Engineering Rutgers University 599 Taylor Rd Piscataway NJ 08854 USA.

Engineering Product Development Singapore University of Technology and Design 8 Somapah Rd Tampines Singapore 487372 Singapore.

出版信息

Adv Nanobiomed Res. 2024 Feb;4(2):2300092. doi: 10.1002/anbr.202300092. Epub 2023 Dec 5.

Abstract

Checkpoint immunotherapy has made great strides in the treatment of solid tumors, but many patients do not respond to immune checkpoint inhibitors. Identification of tumor-infiltrating cytotoxic T cells (CTLs) has the potential to stratify patients and monitor immunotherapy responses. In this study, the design of cluster of differentiation (CD8) T cell-targeted nanoprobes that emit shortwave infrared (SWIR) light in the second tissue-transparent window for noninvasive, real-time imaging of CTLs in murine models of breast cancer is presented. SWIR-emitting rare-earth nanoparticles encapsulated in human serum albumin are conjugated with anti-CD8α to target CTLs with high specificity. CTL targeting is validated in vitro through binding of nanoprobes to primary mouse CTLs. The potential for the use of SWIR fluorescence intensity to determine CTL presence is validated in two syngeneic mammary fat pad tumor models, EMT6 and 4T1, which differ in immune infiltration. SWIR imaging using CD8-targeted nanoprobes successfully identifies the presence of CTLs in the more immunogenic EMT6 model, while imaging confirms the lack of substantial immune infiltration in the nonimmunogenic 4T1 model. In this work, the opportunity for SWIR imaging using CD8-targeted nanoprobes to assess CTL infiltration in tumors for the stratification and monitoring of responders to checkpoint immunotherapy is highlighted.

摘要

检查点免疫疗法在实体瘤治疗方面取得了巨大进展,但许多患者对免疫检查点抑制剂没有反应。识别肿瘤浸润性细胞毒性T细胞(CTL)有潜力对患者进行分层并监测免疫治疗反应。在本研究中,我们展示了一种分化簇(CD8)T细胞靶向纳米探针的设计,该探针在第二个组织透明窗口发射短波红外(SWIR)光,用于在乳腺癌小鼠模型中对CTL进行无创、实时成像。封装在人血清白蛋白中的发射SWIR的稀土纳米颗粒与抗CD8α偶联,以高特异性靶向CTL。通过纳米探针与原代小鼠CTL的结合在体外验证了CTL靶向性。在两种免疫浸润不同的同基因乳腺脂肪垫肿瘤模型EMT6和4T1中,验证了利用SWIR荧光强度确定CTL存在的可能性。使用CD8靶向纳米探针的SWIR成像成功识别了免疫原性更强的EMT6模型中CTL的存在,而成像证实了非免疫原性4T1模型中缺乏大量免疫浸润。在这项工作中,强调了使用CD8靶向纳米探针进行SWIR成像以评估肿瘤中CTL浸润,用于对检查点免疫疗法的反应者进行分层和监测的机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8531/11566364/2785e41d2415/ANBR-4-0-g007.jpg

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