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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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Detalles Bibliográficos
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
Descripción
Sumario: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.