文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

基于放射性核素的分子成像可实现 CAR-T 细胞可视化和治疗监测。

Radionuclide-based molecular imaging allows CAR-T cellular visualization and therapeutic monitoring.

机构信息

Department of Nuclear Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.

Hubei Key Laboratory of Molecular Imaging, Wuhan 430022, China.

出版信息

Theranostics. 2021 May 3;11(14):6800-6817. doi: 10.7150/thno.56989. eCollection 2021.


DOI:10.7150/thno.56989
PMID:34093854
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8171102/
Abstract

Chimeric antigen receptor T cell (CAR-T) therapy is a new and effective form of adoptive cell therapy that is rapidly entering the mainstream for the treatment of CD19-positive hematological cancers because of its impressive effect and durable responses. Huge challenges remain in achieving similar success in patients with solid tumors. The current methods of monitoring CAR-T, including morphological imaging (CT and MRI), blood tests, and biopsy, have limitations to assess whether CAR-T cells are homing to tumor sites and infiltrating into tumor bed, or to assess the survival, proliferation, and persistence of CAR-T cells in solid tumors associated with an immunosuppressive microenvironment. Radionuclide-based molecular imaging affords improved CAR-T cellular visualization and therapeutic monitoring through either a direct cellular radiolabeling approach or a reporter gene imaging strategy, and endogenous cell imaging is beneficial to reflect functional information and immune status of T cells. Focusing on the dynamic monitoring and precise assessment of CAR-T therapy, this review summarizes the current applications of radionuclide-based noninvasive imaging in CAR-T cells visualization and monitoring and presents current challenges and strategic choices.

摘要

嵌合抗原受体 T 细胞(CAR-T)疗法是一种新的、有效的过继细胞疗法,由于其显著的疗效和持久的反应,正在迅速成为治疗 CD19 阳性血液系统恶性肿瘤的主流方法。然而,在实体瘤患者中取得类似的成功仍然面临巨大挑战。目前监测 CAR-T 的方法包括形态学成像(CT 和 MRI)、血液检查和活检,但这些方法都有局限性,无法评估 CAR-T 细胞是否归巢到肿瘤部位并浸润到肿瘤床,也无法评估 CAR-T 细胞在与免疫抑制微环境相关的实体瘤中的存活、增殖和持续存在。放射性核素分子成像通过直接细胞放射性标记或报告基因成像策略提供了对 CAR-T 细胞的可视化和治疗监测的改善,并通过内源性细胞成像有助于反映 T 细胞的功能信息和免疫状态。本综述聚焦于 CAR-T 治疗的动态监测和精确评估,总结了放射性核素非侵入性成像在 CAR-T 细胞可视化和监测中的应用,并提出了当前的挑战和战略选择。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/254531f86ec2/thnov11p6800g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/8dc79125aacf/thnov11p6800g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/50acae8cb622/thnov11p6800g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/6beb9925be3d/thnov11p6800g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/922f51df2d3e/thnov11p6800g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/37cedca0b924/thnov11p6800g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/70ae1738b94b/thnov11p6800g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/dc595f92f25b/thnov11p6800g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/06a7ec9b8fab/thnov11p6800g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/254531f86ec2/thnov11p6800g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/8dc79125aacf/thnov11p6800g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/50acae8cb622/thnov11p6800g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/6beb9925be3d/thnov11p6800g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/922f51df2d3e/thnov11p6800g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/37cedca0b924/thnov11p6800g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/70ae1738b94b/thnov11p6800g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/dc595f92f25b/thnov11p6800g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/06a7ec9b8fab/thnov11p6800g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/886a/8171102/254531f86ec2/thnov11p6800g009.jpg

相似文献

[1]
Radionuclide-based molecular imaging allows CAR-T cellular visualization and therapeutic monitoring.

Theranostics. 2021

[2]
Chimeric antigen receptor-engineered T-cell therapy for liver cancer.

Hepatobiliary Pancreat Dis Int. 2018-5-24

[3]
Effective Targeting of TAG72 Peritoneal Ovarian Tumors via Regional Delivery of CAR-Engineered T Cells.

Front Immunol. 2018-11-19

[4]
Engineering for Success: Approaches to Improve Chimeric Antigen Receptor T Cell Therapy for Solid Tumors.

Drugs. 2019-3

[5]
Making CAR T Cells a Solid Option for Solid Tumors.

Front Immunol. 2018-11-8

[6]
New insights into the pharmacological, immunological, and CAR-T-cell approaches in the treatment of hepatocellular carcinoma.

Drug Resist Updat. 2020-7

[7]
CAR T Cells for Solid Tumors: New Strategies for Finding, Infiltrating, and Surviving in the Tumor Microenvironment.

Front Immunol. 2019-2-5

[8]
Adenovirus-mediated specific tumor tagging facilitates CAR-T therapy against antigen-mismatched solid tumors.

Cancer Lett. 2020-9-1

[9]
Manipulating the tumor microenvironment by adoptive cell transfer of CAR T-cells.

Mamm Genome. 2018-7-9

[10]
Armed with IL-2 based fusion protein improves CAR-T cell fitness and efficacy against solid tumors.

Biochim Biophys Acta Mol Basis Dis. 2024-6

引用本文的文献

[1]
Overcoming barriers in glioblastoma: The potential of CAR T cell immunotherapy.

Theranostics. 2025-6-12

[2]
PET-based tracking of CAR T cells and viral gene transfer using a cell surface reporter that binds to lanthanide complexes.

Nat Biomed Eng. 2025-6-13

[3]
Recent advances in non-invasive tracking of cell-based cancer immunotherapies.

Biomater Sci. 2025-4-8

[4]
Positron emission tomography probes for stem cell monitoring: a review.

Am J Transl Res. 2024-8-15

[5]
Noninvasive longitudinal PET/CT imaging of CAR T cells using PSMA reporter gene.

Eur J Nucl Med Mol Imaging. 2024-3

[6]
Current and potential roles of immuno-PET/-SPECT in CAR T-cell therapy.

Front Med (Lausanne). 2023-6-27

[7]
Biomaterials promote generation and immunotherapy of CAR-T cells.

Front Immunol. 2023

[8]
TGF-β blocking combined with photothermal therapy promote tumor targeted migration and long-term antitumor activity of CAR-T cells.

Mater Today Bio. 2023-3-22

[9]
Molecular MRI-Based Monitoring of Cancer Immunotherapy Treatment Response.

Int J Mol Sci. 2023-2-5

[10]
Immunosuppression in tumor immune microenvironment and its optimization from CAR-T cell therapy.

Theranostics. 2022

本文引用的文献

[1]
Molecular Imaging of Chimeric Antigen Receptor T Cells by ICOS-ImmunoPET.

Clin Cancer Res. 2021-2-15

[2]
Innovative CAR-T Cell Therapy for Solid Tumor; Current Duel between CAR-T Spear and Tumor Shield.

Cancers (Basel). 2020-7-28

[3]
Nuclear imaging approaches facilitating nanomedicine translation.

Adv Drug Deliv Rev. 2020

[4]
Spatiotemporal PET Imaging Reveals Differences in CAR-T Tumor Retention in Triple-Negative Breast Cancer Models.

Mol Ther. 2020-10-7

[5]
CAR-T Cells Hit the Tumor Microenvironment: Strategies to Overcome Tumor Escape.

Front Immunol. 2020

[6]
Imaging Technologies to Monitor the Immune System.

Front Immunol. 2020

[7]
Non-invasive Reporter Gene Imaging of Cell Therapies, including T Cells and Stem Cells.

Mol Ther. 2020-6-3

[8]
ICOS Is an Indicator of T-cell-Mediated Response to Cancer Immunotherapy.

Cancer Res. 2020-3-10

[9]
Chimeric antigen receptor T cells in solid tumors: a war against the tumor microenvironment.

Sci China Life Sci. 2019-12-23

[10]
Imaging CAR T Cell Trafficking with eDHFR as a PET Reporter Gene.

Mol Ther. 2019-10-15

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索