Progress of Molecular Imaging-guided Tumor Immunotherapy

With the development of oncology, immunology and imaging, tumor immunotherapy has been one of the most important strategies for cancer treatment after the classic tumor therapies (chemotherapy, surgery-therapy and radio-therapy). Among them, cytotoxic T lymphocyte-associated protein 4 (CTLA-4) and t...

Full description

Bibliographic Details
Main Authors: GUO Xiaoyi, LIU Fei, HAN Xuedi, ZHU Hua, YANG Zhi
Format: Article
Language:zho
Published: Magazine House of Cancer Research on Prevention and Treatment 2018-01-01
Series:Zhongliu Fangzhi Yanjiu
Subjects:
Online Access:http://html.rhhz.net/ZLFZYJ/html/8578.2018.17.0971.htm
id doaj-1c5ec6f6c784477c8b7676d4ebff5f8e
record_format Article
spelling doaj-1c5ec6f6c784477c8b7676d4ebff5f8e2020-11-25T02:01:03ZzhoMagazine House of Cancer Research on Prevention and TreatmentZhongliu Fangzhi Yanjiu1000-85781000-85782018-01-01451475110.3971/j.issn.1000-8578.2018.17.09718578.2018.17.0971Progress of Molecular Imaging-guided Tumor ImmunotherapyGUO Xiaoyi0LIU Fei1HAN Xuedi2ZHU Hua3YANG Zhi4Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Nuclear Medicine, Peking University Cancer Hospital & Institute, Beijing 100142, ChinaKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Nuclear Medicine, Peking University Cancer Hospital & Institute, Beijing 100142, ChinaKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Nuclear Medicine, Peking University Cancer Hospital & Institute, Beijing 100142, ChinaKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Nuclear Medicine, Peking University Cancer Hospital & Institute, Beijing 100142, ChinaKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Nuclear Medicine, Peking University Cancer Hospital & Institute, Beijing 100142, ChinaWith the development of oncology, immunology and imaging, tumor immunotherapy has been one of the most important strategies for cancer treatment after the classic tumor therapies (chemotherapy, surgery-therapy and radio-therapy). Among them, cytotoxic T lymphocyte-associated protein 4 (CTLA-4) and the programmed cell death protein/protein ligand 1 (anti-PD-1/PD-L1) attract most attention in tumor immunotherapy fields. The CTLA-4 and PD1/PDL1 antibodies can specifically bind and regulate the T cell, enhance the T-cell immune-killer ability to tumors and hold great potential to revolutionize cancer therapy. However, studies have demonstrated the lack of clinical benefit in some patients using immunotherapy. Molecular imaging that based on radio-nuclide labeled immune-therapy antibodies provide a new method for patients selection, response assessment, treatment plan optimization and prognosis assessment by real-time and in-vivo radio-immuno-imaging. This paper based on the existing radio-nuclide labeled immune-therapy antibodies expounds the great change of tumor immunotherapy in the field of molecular imaging in recent years and the research progress of molecular imaging guiding the development of tumor immunotherapy trends.http://html.rhhz.net/ZLFZYJ/html/8578.2018.17.0971.htmtumor immunotherapyimmuno-checkpointmolecular imagingbiomarkerpd1/pd-l1 pathway
collection DOAJ
language zho
format Article
sources DOAJ
author GUO Xiaoyi
LIU Fei
HAN Xuedi
ZHU Hua
YANG Zhi
spellingShingle GUO Xiaoyi
LIU Fei
HAN Xuedi
ZHU Hua
YANG Zhi
Progress of Molecular Imaging-guided Tumor Immunotherapy
Zhongliu Fangzhi Yanjiu
tumor immunotherapy
immuno-checkpoint
molecular imaging
biomarker
pd1/pd-l1 pathway
author_facet GUO Xiaoyi
LIU Fei
HAN Xuedi
ZHU Hua
YANG Zhi
author_sort GUO Xiaoyi
title Progress of Molecular Imaging-guided Tumor Immunotherapy
title_short Progress of Molecular Imaging-guided Tumor Immunotherapy
title_full Progress of Molecular Imaging-guided Tumor Immunotherapy
title_fullStr Progress of Molecular Imaging-guided Tumor Immunotherapy
title_full_unstemmed Progress of Molecular Imaging-guided Tumor Immunotherapy
title_sort progress of molecular imaging-guided tumor immunotherapy
publisher Magazine House of Cancer Research on Prevention and Treatment
series Zhongliu Fangzhi Yanjiu
issn 1000-8578
1000-8578
publishDate 2018-01-01
description With the development of oncology, immunology and imaging, tumor immunotherapy has been one of the most important strategies for cancer treatment after the classic tumor therapies (chemotherapy, surgery-therapy and radio-therapy). Among them, cytotoxic T lymphocyte-associated protein 4 (CTLA-4) and the programmed cell death protein/protein ligand 1 (anti-PD-1/PD-L1) attract most attention in tumor immunotherapy fields. The CTLA-4 and PD1/PDL1 antibodies can specifically bind and regulate the T cell, enhance the T-cell immune-killer ability to tumors and hold great potential to revolutionize cancer therapy. However, studies have demonstrated the lack of clinical benefit in some patients using immunotherapy. Molecular imaging that based on radio-nuclide labeled immune-therapy antibodies provide a new method for patients selection, response assessment, treatment plan optimization and prognosis assessment by real-time and in-vivo radio-immuno-imaging. This paper based on the existing radio-nuclide labeled immune-therapy antibodies expounds the great change of tumor immunotherapy in the field of molecular imaging in recent years and the research progress of molecular imaging guiding the development of tumor immunotherapy trends.
topic tumor immunotherapy
immuno-checkpoint
molecular imaging
biomarker
pd1/pd-l1 pathway
url http://html.rhhz.net/ZLFZYJ/html/8578.2018.17.0971.htm
work_keys_str_mv AT guoxiaoyi progressofmolecularimagingguidedtumorimmunotherapy
AT liufei progressofmolecularimagingguidedtumorimmunotherapy
AT hanxuedi progressofmolecularimagingguidedtumorimmunotherapy
AT zhuhua progressofmolecularimagingguidedtumorimmunotherapy
AT yangzhi progressofmolecularimagingguidedtumorimmunotherapy
_version_ 1724959141884067840