He Shasha, Cheng Penghui, Pu Kanyi
School of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University, Singapore, Singapore.
Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore, Singapore.
Nat Biomed Eng. 2023 Mar;7(3):281-297. doi: 10.1038/s41551-023-01009-1. Epub 2023 Mar 20.
Tracking the immune microenvironment of tumours is essential for understanding the mechanisms behind the effectiveness of cancer immunotherapies. Molecular imaging of tumour-infiltrating leukocytes (TILs) can be used to non-invasively monitor the tumour immune microenvironment, but current imaging agents do not distinguish TILs from leukocytes resident in other tissues. Here we report a library of activatable molecular probes for the imaging, via near-infrared fluorescence, of specific TILs (including M1 macrophages, cytotoxic T lymphocytes and neutrophils) in vivo in real time and also via excreted urine, owing to the probes' renal clearance. The fluorescence of the probes is activated only in the presence of both tumour and leukocyte biomarkers, which allows for the imaging of populations of specific TILs in mouse models of cancers with sensitivities and specificities similar to those achieved via flow-cytometric analyses of biopsied tumour tissues. We also show that the probes enable the non-invasive evaluation of the immunogenicity of different tumours, the dynamic monitoring of responses to immunotherapies and the accurate prediction of tumour growth under various treatments.
追踪肿瘤的免疫微环境对于理解癌症免疫疗法有效性背后的机制至关重要。肿瘤浸润白细胞(TILs)的分子成像可用于非侵入性监测肿瘤免疫微环境,但目前的成像剂无法区分TILs与其他组织中的常驻白细胞。在此,我们报告了一个可激活分子探针库,该探针库能够通过近红外荧光在体内实时成像特定的TILs(包括M1巨噬细胞、细胞毒性T淋巴细胞和中性粒细胞),并且由于探针的肾脏清除作用,还能通过排泄的尿液进行成像。这些探针的荧光仅在肿瘤和白细胞生物标志物同时存在时被激活,这使得在癌症小鼠模型中对特定TILs群体进行成像成为可能,其灵敏度和特异性与通过对活检肿瘤组织进行流式细胞术分析所达到的类似。我们还表明,这些探针能够对不同肿瘤的免疫原性进行非侵入性评估,对免疫疗法的反应进行动态监测,并在各种治疗下准确预测肿瘤生长。