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Preclinical Evaluation of Podoplanin-Targeted Alpha-Radioimmunotherapy with the Novel Antibody NZ-16 for Malignant Mesothelioma

The prognosis of advanced mesothelioma is poor. Podoplanin (PDPN) is highly expressed in most malignant mesothelioma. This study aimed to evaluate the potential alpha-radioimmunotherapy (RIT) with a newly developed anti-PDPN antibody, NZ-16, compared with a previous antibody, NZ-12. Methods: The in...

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Autores principales: Sudo, Hitomi, Tsuji, Atsushi B., Sugyo, Aya, Kaneko, Mika K., Kato, Yukinari, Nagatsu, Kotaro, Suzuki, Hisashi, Higashi, Tatsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533940/
https://www.ncbi.nlm.nih.gov/pubmed/34685483
http://dx.doi.org/10.3390/cells10102503
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author Sudo, Hitomi
Tsuji, Atsushi B.
Sugyo, Aya
Kaneko, Mika K.
Kato, Yukinari
Nagatsu, Kotaro
Suzuki, Hisashi
Higashi, Tatsuya
author_facet Sudo, Hitomi
Tsuji, Atsushi B.
Sugyo, Aya
Kaneko, Mika K.
Kato, Yukinari
Nagatsu, Kotaro
Suzuki, Hisashi
Higashi, Tatsuya
author_sort Sudo, Hitomi
collection PubMed
description The prognosis of advanced mesothelioma is poor. Podoplanin (PDPN) is highly expressed in most malignant mesothelioma. This study aimed to evaluate the potential alpha-radioimmunotherapy (RIT) with a newly developed anti-PDPN antibody, NZ-16, compared with a previous antibody, NZ-12. Methods: The in vitro properties of radiolabeled antibodies were evaluated by cell binding and competitive inhibition assays using PDPN-expressing H226 mesothelioma cells. The biodistribution of (111)In-labeled antibodies was studied in tumor-bearing mice. The absorbed doses were estimated based on biodistribution data. Tumor volumes and body weights of mice treated with (90)Y- and (225)Ac-labeled NZ-16 were measured for 56 days. Histologic analysis was conducted. Results: The radiolabeled NZ-16 specifically bound to H226 cells with higher affinity than NZ-12. The biodistribution studies showed higher tumor uptake of radiolabeled NZ-16 compared with NZ-12, providing higher absorbed doses to tumors. RIT with (225)Ac- and (90)Y-labeled NZ-16 had a significantly higher antitumor effect than RIT with (90)Y-labeled NZ-12. (225)Ac-labeled NZ-16 induced a larger amount of necrotic change and showed a tendency to suppress tumor volumes and prolonged survival than (90)Y-labeled NZ-16. There is no obvious adverse effect. Conclusions: Alpha-RIT with the newly developed NZ-16 is a promising therapeutic option for malignant mesothelioma.
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spelling pubmed-85339402021-10-23 Preclinical Evaluation of Podoplanin-Targeted Alpha-Radioimmunotherapy with the Novel Antibody NZ-16 for Malignant Mesothelioma Sudo, Hitomi Tsuji, Atsushi B. Sugyo, Aya Kaneko, Mika K. Kato, Yukinari Nagatsu, Kotaro Suzuki, Hisashi Higashi, Tatsuya Cells Article The prognosis of advanced mesothelioma is poor. Podoplanin (PDPN) is highly expressed in most malignant mesothelioma. This study aimed to evaluate the potential alpha-radioimmunotherapy (RIT) with a newly developed anti-PDPN antibody, NZ-16, compared with a previous antibody, NZ-12. Methods: The in vitro properties of radiolabeled antibodies were evaluated by cell binding and competitive inhibition assays using PDPN-expressing H226 mesothelioma cells. The biodistribution of (111)In-labeled antibodies was studied in tumor-bearing mice. The absorbed doses were estimated based on biodistribution data. Tumor volumes and body weights of mice treated with (90)Y- and (225)Ac-labeled NZ-16 were measured for 56 days. Histologic analysis was conducted. Results: The radiolabeled NZ-16 specifically bound to H226 cells with higher affinity than NZ-12. The biodistribution studies showed higher tumor uptake of radiolabeled NZ-16 compared with NZ-12, providing higher absorbed doses to tumors. RIT with (225)Ac- and (90)Y-labeled NZ-16 had a significantly higher antitumor effect than RIT with (90)Y-labeled NZ-12. (225)Ac-labeled NZ-16 induced a larger amount of necrotic change and showed a tendency to suppress tumor volumes and prolonged survival than (90)Y-labeled NZ-16. There is no obvious adverse effect. Conclusions: Alpha-RIT with the newly developed NZ-16 is a promising therapeutic option for malignant mesothelioma. MDPI 2021-09-22 /pmc/articles/PMC8533940/ /pubmed/34685483 http://dx.doi.org/10.3390/cells10102503 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sudo, Hitomi
Tsuji, Atsushi B.
Sugyo, Aya
Kaneko, Mika K.
Kato, Yukinari
Nagatsu, Kotaro
Suzuki, Hisashi
Higashi, Tatsuya
Preclinical Evaluation of Podoplanin-Targeted Alpha-Radioimmunotherapy with the Novel Antibody NZ-16 for Malignant Mesothelioma
title Preclinical Evaluation of Podoplanin-Targeted Alpha-Radioimmunotherapy with the Novel Antibody NZ-16 for Malignant Mesothelioma
title_full Preclinical Evaluation of Podoplanin-Targeted Alpha-Radioimmunotherapy with the Novel Antibody NZ-16 for Malignant Mesothelioma
title_fullStr Preclinical Evaluation of Podoplanin-Targeted Alpha-Radioimmunotherapy with the Novel Antibody NZ-16 for Malignant Mesothelioma
title_full_unstemmed Preclinical Evaluation of Podoplanin-Targeted Alpha-Radioimmunotherapy with the Novel Antibody NZ-16 for Malignant Mesothelioma
title_short Preclinical Evaluation of Podoplanin-Targeted Alpha-Radioimmunotherapy with the Novel Antibody NZ-16 for Malignant Mesothelioma
title_sort preclinical evaluation of podoplanin-targeted alpha-radioimmunotherapy with the novel antibody nz-16 for malignant mesothelioma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8533940/
https://www.ncbi.nlm.nih.gov/pubmed/34685483
http://dx.doi.org/10.3390/cells10102503
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