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Evaluation of (124)I-JS001 for hPD1 immuno-PET imaging using sarcoma cell homografts in humanized mice

JS001 (toripalimab) is a humanized IgG monoclonal antibody which strongly inhibits programmed cell death protein 1 (PD1). In this study, we used a different iodine isotype ((nat/124/125)I) to label JS001 probes to target the human PD1 (hPD1) antigen. In vitro, the half maximal effective concentratio...

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Autores principales: Huang, Haifeng, Zhu, Hua, Xie, Quan, Tian, Xiaobin, Yang, Xianteng, Feng, Fan, Jiang, Qiyu, Sheng, Xinan, Yang, Zhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7452040/
https://www.ncbi.nlm.nih.gov/pubmed/32874831
http://dx.doi.org/10.1016/j.apsb.2020.02.004
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author Huang, Haifeng
Zhu, Hua
Xie, Quan
Tian, Xiaobin
Yang, Xianteng
Feng, Fan
Jiang, Qiyu
Sheng, Xinan
Yang, Zhi
author_facet Huang, Haifeng
Zhu, Hua
Xie, Quan
Tian, Xiaobin
Yang, Xianteng
Feng, Fan
Jiang, Qiyu
Sheng, Xinan
Yang, Zhi
author_sort Huang, Haifeng
collection PubMed
description JS001 (toripalimab) is a humanized IgG monoclonal antibody which strongly inhibits programmed cell death protein 1 (PD1). In this study, we used a different iodine isotype ((nat/124/125)I) to label JS001 probes to target the human PD1 (hPD1) antigen. In vitro, the half maximal effective concentration (EC(50)) value of (nat)I-JS001 did not significantly differ from that of JS001. The uptake of (125)I-JS001 by activated T cells was 5.63 times higher than that by nonactivated T cells after 2 h of incubation. The binding affinity of (125)I-JS001 to T cells of different lineages after phytohemagglutinin (PHA) stimulation reached 4.26 nmol/L. Humanized PD1 C57BL/6 mice bearing mouse sarcoma S180 cell tumors were validated for immuno-positron emission tomography (immuno-PET) imaging. Pathological staining was used to assess the expression of PD1 in tumor tissues. The homologous (124)I-human IgG ((124)I-hIgG) group or blocking group was used as a control group. Immuno-PET imaging showed that the uptake in the tumor area of the (124)I-JS001 group at different time points was significantly higher than that of the blocking group or the (124)I-hIgG group in the humanized PD1 mouse model. Taken together, these results suggest that this radiotracer has potential for noninvasive monitoring and directing tumor-specific personalized immunotherapy in PD1-positive tumors.
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spelling pubmed-74520402020-08-31 Evaluation of (124)I-JS001 for hPD1 immuno-PET imaging using sarcoma cell homografts in humanized mice Huang, Haifeng Zhu, Hua Xie, Quan Tian, Xiaobin Yang, Xianteng Feng, Fan Jiang, Qiyu Sheng, Xinan Yang, Zhi Acta Pharm Sin B Original article JS001 (toripalimab) is a humanized IgG monoclonal antibody which strongly inhibits programmed cell death protein 1 (PD1). In this study, we used a different iodine isotype ((nat/124/125)I) to label JS001 probes to target the human PD1 (hPD1) antigen. In vitro, the half maximal effective concentration (EC(50)) value of (nat)I-JS001 did not significantly differ from that of JS001. The uptake of (125)I-JS001 by activated T cells was 5.63 times higher than that by nonactivated T cells after 2 h of incubation. The binding affinity of (125)I-JS001 to T cells of different lineages after phytohemagglutinin (PHA) stimulation reached 4.26 nmol/L. Humanized PD1 C57BL/6 mice bearing mouse sarcoma S180 cell tumors were validated for immuno-positron emission tomography (immuno-PET) imaging. Pathological staining was used to assess the expression of PD1 in tumor tissues. The homologous (124)I-human IgG ((124)I-hIgG) group or blocking group was used as a control group. Immuno-PET imaging showed that the uptake in the tumor area of the (124)I-JS001 group at different time points was significantly higher than that of the blocking group or the (124)I-hIgG group in the humanized PD1 mouse model. Taken together, these results suggest that this radiotracer has potential for noninvasive monitoring and directing tumor-specific personalized immunotherapy in PD1-positive tumors. Elsevier 2020-07 2020-02-19 /pmc/articles/PMC7452040/ /pubmed/32874831 http://dx.doi.org/10.1016/j.apsb.2020.02.004 Text en © 2020 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original article
Huang, Haifeng
Zhu, Hua
Xie, Quan
Tian, Xiaobin
Yang, Xianteng
Feng, Fan
Jiang, Qiyu
Sheng, Xinan
Yang, Zhi
Evaluation of (124)I-JS001 for hPD1 immuno-PET imaging using sarcoma cell homografts in humanized mice
title Evaluation of (124)I-JS001 for hPD1 immuno-PET imaging using sarcoma cell homografts in humanized mice
title_full Evaluation of (124)I-JS001 for hPD1 immuno-PET imaging using sarcoma cell homografts in humanized mice
title_fullStr Evaluation of (124)I-JS001 for hPD1 immuno-PET imaging using sarcoma cell homografts in humanized mice
title_full_unstemmed Evaluation of (124)I-JS001 for hPD1 immuno-PET imaging using sarcoma cell homografts in humanized mice
title_short Evaluation of (124)I-JS001 for hPD1 immuno-PET imaging using sarcoma cell homografts in humanized mice
title_sort evaluation of (124)i-js001 for hpd1 immuno-pet imaging using sarcoma cell homografts in humanized mice
topic Original article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7452040/
https://www.ncbi.nlm.nih.gov/pubmed/32874831
http://dx.doi.org/10.1016/j.apsb.2020.02.004
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