纳米探针
生物医学中的光声成像
颗粒酶B
荧光
菁
细胞毒性T细胞
荧光寿命成像显微镜
化学
分子成像
免疫系统
免疫疗法
共轭体系
材料科学
体内
癌症研究
生物物理学
纳米技术
聚合物
医学
体外
免疫学
生物化学
生物
光学
纳米颗粒
有机化学
生物技术
物理
作者
Yan Zhang,Shasha He,Wan Chen,Yinghua Liu,Xuefei Zhang,Qingqing Miao,Kanyi Pu
标识
DOI:10.1002/anie.202015116
摘要
Abstract Development of real‐time non‐invasive imaging probes to assess infiltration and activation of cytotoxic T cells (CTLs) is critical to predict the efficacy of cancer immunotherapy, which however remains challenging. Reported here is an activatable semiconducting polymer nanoprobe (SPNP) for near‐infrared fluorescence (NIRF) and photoacoustic (PA) imaging of a biomarker (granzyme B) associated with activation of CTLs. SPNP comprises a semiconducting polymer (SP) conjugated with a granzyme B cleavable and dye‐labeled peptide as the side chain, both of which emit NIRF and PA signals. After systemic administration, SPNP passively targets the tumor and in situ reacts with granzyme B to release the dye‐labeled peptide, leading to decreased NIRF and PA signals from the dye but unchanged signals from the polymer. Such ratiometric NIRF and PA signals of SPNP correlate well with the expression level of granzyme B and intratumoral population of CTLs. Thus, this study not only presents the first PA probes for in vivo imaging of immune activation but also provides a molecular design strategy that can be generalized for molecular imaging of other immune‐related biomarkers.
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