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Implication of (99m)Tc-sum IL-2 SPECT/CT in immunotherapy by imaging of tumor-infiltrating T cells

BACKGROUND: Although immune checkpoint blockade (ICB) and adoptive T cell transfer (ACT) therapy have achieved impressive clinical outcomes, majority of patients do not respond to immunotherapy. Tumor-infiltrating T cells, a critical factor to immunotherapy, is dynamically changing. Therefore, a rel...

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Autores principales: Gao, Yu, Luo, Qi, Sun, Zhichen, Gao, Hannan, Yu, Yue, Sun, Yining, Ma, Xiaotu, Han, Chuanhui, Shi, Jiyun, Wang, Fan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980373/
https://www.ncbi.nlm.nih.gov/pubmed/36858461
http://dx.doi.org/10.1136/jitc-2022-005925
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author Gao, Yu
Luo, Qi
Sun, Zhichen
Gao, Hannan
Yu, Yue
Sun, Yining
Ma, Xiaotu
Han, Chuanhui
Shi, Jiyun
Wang, Fan
author_facet Gao, Yu
Luo, Qi
Sun, Zhichen
Gao, Hannan
Yu, Yue
Sun, Yining
Ma, Xiaotu
Han, Chuanhui
Shi, Jiyun
Wang, Fan
author_sort Gao, Yu
collection PubMed
description BACKGROUND: Although immune checkpoint blockade (ICB) and adoptive T cell transfer (ACT) therapy have achieved impressive clinical outcomes, majority of patients do not respond to immunotherapy. Tumor-infiltrating T cells, a critical factor to immunotherapy, is dynamically changing. Therefore, a reliable real-time in vivo imaging system for tumor-infiltrating T cells, but not immunohistochemical analyses, will be more valuable to predict response and guide immunotherapy. In this study, we developed a new SPECT/CT imaging probe (99m)Tc-sum IL-2 targeting the IL-2Rβ/IL-2Rγ (CD122/CD132) receptor on tumor-infiltrating T cells, and evaluated its application in predicting the immune response to anti-PD-L1 (αPD-L1) therapy as well as tracking infused T cells in ACT therapy. METHODS: The binding affinity of the super mutated IL-2 (sum IL-2) in various T cell subtypes was measured. Sum IL-2 was subsequently labeled with (99m)Tc through Sortase-A mediated site-specific transpeptidation. SPECT/CT imaging and biodistribution studies of (99m)Tc-sum IL-2 were performed in a MC38 mouse model. Wild type IL-2 (IL-2) was used as control in the above studies. Finally, we evaluated (99m)Tc-sum IL-2 SPECT/CT for the detection of tumor-infiltrating T cells in the context of αPD-L1 immunotherapy and ACT therapy. RESULTS: Sum IL-2 preferentially bound to CD8(+) T cells, especially activated CD8(+) T cells, while IL-2 showed biased binding to Treg cells. As a result, (99m)Tc-sum IL-2 could detect tumor-infiltrating T cells. In the MC38 tumor model, SPECT/CT imaging showed the increased tumor uptake of (99m)Tc-sum IL-2 after αPD-L1 treatment, suggesting that the treatment significantly increased tumor-infiltrating T cells, resulting in a correspondingly significant curative effect. In addition, (99m)Tc-sum IL-2 SPECT/CT could also track the infiltration of antigen-specific cytotoxic CD8(+) T cells during ACT therapy. CONCLUSION: (99m)Tc-sum IL-2 has great clinical potential for non-invasive and specific SPECT/CT imaging of tumor-infiltrating T cells as well as for timely prediction and evaluation of the therapeutic efficacy of ICB and ACT therapy.
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spelling pubmed-99803732023-03-03 Implication of (99m)Tc-sum IL-2 SPECT/CT in immunotherapy by imaging of tumor-infiltrating T cells Gao, Yu Luo, Qi Sun, Zhichen Gao, Hannan Yu, Yue Sun, Yining Ma, Xiaotu Han, Chuanhui Shi, Jiyun Wang, Fan J Immunother Cancer Basic Tumor Immunology BACKGROUND: Although immune checkpoint blockade (ICB) and adoptive T cell transfer (ACT) therapy have achieved impressive clinical outcomes, majority of patients do not respond to immunotherapy. Tumor-infiltrating T cells, a critical factor to immunotherapy, is dynamically changing. Therefore, a reliable real-time in vivo imaging system for tumor-infiltrating T cells, but not immunohistochemical analyses, will be more valuable to predict response and guide immunotherapy. In this study, we developed a new SPECT/CT imaging probe (99m)Tc-sum IL-2 targeting the IL-2Rβ/IL-2Rγ (CD122/CD132) receptor on tumor-infiltrating T cells, and evaluated its application in predicting the immune response to anti-PD-L1 (αPD-L1) therapy as well as tracking infused T cells in ACT therapy. METHODS: The binding affinity of the super mutated IL-2 (sum IL-2) in various T cell subtypes was measured. Sum IL-2 was subsequently labeled with (99m)Tc through Sortase-A mediated site-specific transpeptidation. SPECT/CT imaging and biodistribution studies of (99m)Tc-sum IL-2 were performed in a MC38 mouse model. Wild type IL-2 (IL-2) was used as control in the above studies. Finally, we evaluated (99m)Tc-sum IL-2 SPECT/CT for the detection of tumor-infiltrating T cells in the context of αPD-L1 immunotherapy and ACT therapy. RESULTS: Sum IL-2 preferentially bound to CD8(+) T cells, especially activated CD8(+) T cells, while IL-2 showed biased binding to Treg cells. As a result, (99m)Tc-sum IL-2 could detect tumor-infiltrating T cells. In the MC38 tumor model, SPECT/CT imaging showed the increased tumor uptake of (99m)Tc-sum IL-2 after αPD-L1 treatment, suggesting that the treatment significantly increased tumor-infiltrating T cells, resulting in a correspondingly significant curative effect. In addition, (99m)Tc-sum IL-2 SPECT/CT could also track the infiltration of antigen-specific cytotoxic CD8(+) T cells during ACT therapy. CONCLUSION: (99m)Tc-sum IL-2 has great clinical potential for non-invasive and specific SPECT/CT imaging of tumor-infiltrating T cells as well as for timely prediction and evaluation of the therapeutic efficacy of ICB and ACT therapy. BMJ Publishing Group 2023-03-01 /pmc/articles/PMC9980373/ /pubmed/36858461 http://dx.doi.org/10.1136/jitc-2022-005925 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Basic Tumor Immunology
Gao, Yu
Luo, Qi
Sun, Zhichen
Gao, Hannan
Yu, Yue
Sun, Yining
Ma, Xiaotu
Han, Chuanhui
Shi, Jiyun
Wang, Fan
Implication of (99m)Tc-sum IL-2 SPECT/CT in immunotherapy by imaging of tumor-infiltrating T cells
title Implication of (99m)Tc-sum IL-2 SPECT/CT in immunotherapy by imaging of tumor-infiltrating T cells
title_full Implication of (99m)Tc-sum IL-2 SPECT/CT in immunotherapy by imaging of tumor-infiltrating T cells
title_fullStr Implication of (99m)Tc-sum IL-2 SPECT/CT in immunotherapy by imaging of tumor-infiltrating T cells
title_full_unstemmed Implication of (99m)Tc-sum IL-2 SPECT/CT in immunotherapy by imaging of tumor-infiltrating T cells
title_short Implication of (99m)Tc-sum IL-2 SPECT/CT in immunotherapy by imaging of tumor-infiltrating T cells
title_sort implication of (99m)tc-sum il-2 spect/ct in immunotherapy by imaging of tumor-infiltrating t cells
topic Basic Tumor Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9980373/
https://www.ncbi.nlm.nih.gov/pubmed/36858461
http://dx.doi.org/10.1136/jitc-2022-005925
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