Next Generation of Solid Target Radionuclide Antibody Conjugates for Tumor Immuno‐Therapy

ABSTRACT Immune checkpoint therapy has emerged as an effective treatment option for various types of cancers. Key immune checkpoint molecules, such as cytotoxic T‐lymphocyte‐associated protein 4 (CTLA‐4), programmed cell death protein 1 (PD‐1), and lymphocyte activation gene 3 (LAG‐3), have become p...

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Veröffentlicht in:Journal of labelled compounds & radiopharmaceuticals 2024-10, Vol.67 (12-13), p.396-409
Hauptverfasser: Hou, Xingguo, Kong, Xiangxing, Yao, Yuan, Liu, Song, Ren, Ya'nan, Hu, Muye, Wang, Zilei, Zhu, Hua, Yang, Zhi
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container_end_page 409
container_issue 12-13
container_start_page 396
container_title Journal of labelled compounds & radiopharmaceuticals
container_volume 67
creator Hou, Xingguo
Kong, Xiangxing
Yao, Yuan
Liu, Song
Ren, Ya'nan
Hu, Muye
Wang, Zilei
Zhu, Hua
Yang, Zhi
description ABSTRACT Immune checkpoint therapy has emerged as an effective treatment option for various types of cancers. Key immune checkpoint molecules, such as cytotoxic T‐lymphocyte‐associated protein 4 (CTLA‐4), programmed cell death protein 1 (PD‐1), and lymphocyte activation gene 3 (LAG‐3), have become pivotal targets in cancer immunotherapy. Antibodies designed to inhibit these molecules have demonstrated significant clinical efficacy. Nevertheless, the ability to monitor changes in the immune status of tumors and predict treatment response remains limited. Conventional methods, such as assessing lymphocytes in peripheral blood or conducting tumor biopsies, are inadequate for providing real‐time, spatial information about T‐cell distributions within heterogeneous tumors. Positron emission tomography (PET) using T‐cell specific probes represents a promising and noninvasive approach to monitor both systemic and intratumoral immune changes during treatment. This technique holds substantial clinical significance and potential utility. In this paper, we review the applications of PET probes that target immune cells in molecular imaging. The three solid target radio nuclides and imaging of solid target nuclide‐labeled probes.
doi_str_mv 10.1002/jlcr.4124
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Key immune checkpoint molecules, such as cytotoxic T‐lymphocyte‐associated protein 4 (CTLA‐4), programmed cell death protein 1 (PD‐1), and lymphocyte activation gene 3 (LAG‐3), have become pivotal targets in cancer immunotherapy. Antibodies designed to inhibit these molecules have demonstrated significant clinical efficacy. Nevertheless, the ability to monitor changes in the immune status of tumors and predict treatment response remains limited. Conventional methods, such as assessing lymphocytes in peripheral blood or conducting tumor biopsies, are inadequate for providing real‐time, spatial information about T‐cell distributions within heterogeneous tumors. Positron emission tomography (PET) using T‐cell specific probes represents a promising and noninvasive approach to monitor both systemic and intratumoral immune changes during treatment. This technique holds substantial clinical significance and potential utility. In this paper, we review the applications of PET probes that target immune cells in molecular imaging. 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subjects Animals
Antibodies
Apoptosis
Biopsy
Cancer
Cancer immunotherapy
Cell activation
Cell death
copper‐64
Cytotoxicity
Effectiveness
Humans
Immune checkpoint
immune checkpoint therapy
Immune status
Immune system
Immunoconjugates - chemistry
Immunoconjugates - therapeutic use
immunotherapy
Immunotherapy - methods
iodine‐124
isotope labeling
Lymphocytes
Neoplasms - diagnostic imaging
Neoplasms - immunology
Neoplasms - therapy
noninvasive monitoring
PD-1 protein
Peripheral blood
Positron emission
Positron emission tomography
Positron-Emission Tomography - methods
Probes
Proteins
Radioisotopes
Radioisotopes - chemistry
Radioisotopes - therapeutic use
solid target
Spatial data
T cells
Tumors
zirconium‐89
title Next Generation of Solid Target Radionuclide Antibody Conjugates for Tumor Immuno‐Therapy
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