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Cell Model for Testing Pharmaceuticals Targeting Human PD-L1

Cell Model for Testing Pharmaceuticals Targeting Human PD-L1

Shashkova O.A., Terekhina L.A., Malakhov I.S., Pinevich A.A., Vartanyan N.L., Avrov K.O., Krutetskaya I.Yu., Gryazeva I.V., Berlina M.A., Stolbovaya A.Yu., Smirnov I.V., Fedorenko S.V., Krylova A.A., Nadporojskii M.A., Shatik S.V., Stanzhevskii A.A., Samoilovich M.P.
Key words: PD-L1; radioconjugate; VHH; cell model; CT26; targeted agent; tumor model.
2024, volume 16, issue 5, page 5.

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The aim of this study was to create and evaluate a cell model designed for in vitro and in vivo testing of anti-human PD-L1 therapeutic and diagnostic agents’ specificity.

Materials and Methods. Genetically modified cells expressing human PD-L1 (strain CT26-PD-L1) were obtained by retroviral transduction of murine CT26 carcinoma cells. PD-L1 gene activity was assessed by real-time PCR, and PD-L1 expression on cells was identified by flow cytometry. Cells were tested using recombinant single-domain human anti-PD-L1 antibodies (nanoantibodies) conjugated with radioisotopes 68Ga or 177Lu. Immunoreactive fraction and cell internalization of the radioconjugates were evaluated in vitro. For in vivo experiments CT26-PD-L1 cells were transplanted into mice, radioimmunoconjugates were injected 9–14 days later, in 1–48 h the tumors were retrieved and subjected to direct radiometry. Intact CT26 cells not expressing the antigen served as a control.

Results. CT26-PD-L1 strain of murine tumor cells expressing human membrane PD-L1 was created. When transplanted into intact BALB/c mice or sublethally irradiated F1(DBA×BALB/c) mice, these cells formed tumors. Thus, a significant advantage of the model was the possibility of in vivo testing of human PD-L1-affinity agents using animals under conventional vivarium conditions. When radioimmunoconjugates were administered to tumor bearing mice, radionuclides accumulated in tumors generated from the transplanted CT26-PD-L1 cells, but not CT26 cells. CT26-PD-L1 cells internalized anti-PD-L1 nanobodies in vitro. Due to a high density of target molecules, CT26-PD-L1 cells allowed both to confirm pharmaceuticals’ specificity and to quantify the target-binding fraction of conjugates in a single test.

Conclusion. The created cells are the first genetically engineered cells designed to evaluate affinity of anti-human PD-L1 therapeutic and diagnostic agents in Russia. Test results confirmed the model suitability for in vitro and in vivo testing of the specificity of pharmaceuticals targeting human PD-L1.

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Shashkova O.A., Terekhina L.A., Malakhov I.S., Pinevich A.A., Vartanyan N.L., Avrov K.O., Krutetskaya I.Yu., Gryazeva I.V., Berlina M.A., Stolbovaya A.Yu., Smirnov I.V., Fedorenko S.V., Krylova A.A., Nadporojskii M.A., Shatik S.V., Stanzhevskii A.A., Samoilovich M.P. Cell Model for Testing Pharmaceuticals Targeting Human PD-L1. Sovremennye tehnologii v medicine 2024; 16(5): 5, https://doi.org/10.17691/stm2024.16.5.01


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