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A VEGF receptor vaccine demonstrates preliminary efficacy in neurofibromatosis type 2

The anti-VEGF antibody bevacizumab has shown efficacy for the treatment of neurofibromatosis type 2 (NF2). Theoretically, vascular endothelial growth factor receptors (VEGFRs)-specific cytotoxic T lymphocytes (CTLs) can kill both tumor vessel cells and tumor cells expressing VEGFRs. Here we show an...

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Autores principales: Tamura, Ryota, Fujioka, Masato, Morimoto, Yukina, Ohara, Kentaro, Kosugi, Kenzo, Oishi, Yumiko, Sato, Mizuto, Ueda, Ryo, Fujiwara, Hirokazu, Hikichi, Tetsuro, Noji, Shinobu, Oishi, Naoki, Ogawa, Kaoru, Kawakami, Yutaka, Ohira, Takayuki, Yoshida, Kazunari, Toda, Masahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917794/
https://www.ncbi.nlm.nih.gov/pubmed/31848332
http://dx.doi.org/10.1038/s41467-019-13640-1
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author Tamura, Ryota
Fujioka, Masato
Morimoto, Yukina
Ohara, Kentaro
Kosugi, Kenzo
Oishi, Yumiko
Sato, Mizuto
Ueda, Ryo
Fujiwara, Hirokazu
Hikichi, Tetsuro
Noji, Shinobu
Oishi, Naoki
Ogawa, Kaoru
Kawakami, Yutaka
Ohira, Takayuki
Yoshida, Kazunari
Toda, Masahiro
author_facet Tamura, Ryota
Fujioka, Masato
Morimoto, Yukina
Ohara, Kentaro
Kosugi, Kenzo
Oishi, Yumiko
Sato, Mizuto
Ueda, Ryo
Fujiwara, Hirokazu
Hikichi, Tetsuro
Noji, Shinobu
Oishi, Naoki
Ogawa, Kaoru
Kawakami, Yutaka
Ohira, Takayuki
Yoshida, Kazunari
Toda, Masahiro
author_sort Tamura, Ryota
collection PubMed
description The anti-VEGF antibody bevacizumab has shown efficacy for the treatment of neurofibromatosis type 2 (NF2). Theoretically, vascular endothelial growth factor receptors (VEGFRs)-specific cytotoxic T lymphocytes (CTLs) can kill both tumor vessel cells and tumor cells expressing VEGFRs. Here we show an exploratory clinical study of VEGFRs peptide vaccine in seven patients with progressive NF2-derived schwannomas. Hearing improves in 2/5 assessable patients (40%) as determined by international guidelines, with increases in word recognition scores. Tumor volume reductions of ≥20% are observed in two patients, including one in which bevacizumab had not been effective. There are no severe adverse events related to the vaccine. Both VEGFR1-specific and VEGFR2-specific CTLs are induced in six patients. Surgery is performed after vaccination in two patients, and significant reductions in the expression of VEGFRs in schwannomas are observed. Therefore, this clinical immunotherapy study demonstrates the safety and preliminary efficacy of VEGFRs peptide vaccination in patients with NF2.
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spelling pubmed-69177942019-12-19 A VEGF receptor vaccine demonstrates preliminary efficacy in neurofibromatosis type 2 Tamura, Ryota Fujioka, Masato Morimoto, Yukina Ohara, Kentaro Kosugi, Kenzo Oishi, Yumiko Sato, Mizuto Ueda, Ryo Fujiwara, Hirokazu Hikichi, Tetsuro Noji, Shinobu Oishi, Naoki Ogawa, Kaoru Kawakami, Yutaka Ohira, Takayuki Yoshida, Kazunari Toda, Masahiro Nat Commun Article The anti-VEGF antibody bevacizumab has shown efficacy for the treatment of neurofibromatosis type 2 (NF2). Theoretically, vascular endothelial growth factor receptors (VEGFRs)-specific cytotoxic T lymphocytes (CTLs) can kill both tumor vessel cells and tumor cells expressing VEGFRs. Here we show an exploratory clinical study of VEGFRs peptide vaccine in seven patients with progressive NF2-derived schwannomas. Hearing improves in 2/5 assessable patients (40%) as determined by international guidelines, with increases in word recognition scores. Tumor volume reductions of ≥20% are observed in two patients, including one in which bevacizumab had not been effective. There are no severe adverse events related to the vaccine. Both VEGFR1-specific and VEGFR2-specific CTLs are induced in six patients. Surgery is performed after vaccination in two patients, and significant reductions in the expression of VEGFRs in schwannomas are observed. Therefore, this clinical immunotherapy study demonstrates the safety and preliminary efficacy of VEGFRs peptide vaccination in patients with NF2. Nature Publishing Group UK 2019-12-17 /pmc/articles/PMC6917794/ /pubmed/31848332 http://dx.doi.org/10.1038/s41467-019-13640-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Tamura, Ryota
Fujioka, Masato
Morimoto, Yukina
Ohara, Kentaro
Kosugi, Kenzo
Oishi, Yumiko
Sato, Mizuto
Ueda, Ryo
Fujiwara, Hirokazu
Hikichi, Tetsuro
Noji, Shinobu
Oishi, Naoki
Ogawa, Kaoru
Kawakami, Yutaka
Ohira, Takayuki
Yoshida, Kazunari
Toda, Masahiro
A VEGF receptor vaccine demonstrates preliminary efficacy in neurofibromatosis type 2
title A VEGF receptor vaccine demonstrates preliminary efficacy in neurofibromatosis type 2
title_full A VEGF receptor vaccine demonstrates preliminary efficacy in neurofibromatosis type 2
title_fullStr A VEGF receptor vaccine demonstrates preliminary efficacy in neurofibromatosis type 2
title_full_unstemmed A VEGF receptor vaccine demonstrates preliminary efficacy in neurofibromatosis type 2
title_short A VEGF receptor vaccine demonstrates preliminary efficacy in neurofibromatosis type 2
title_sort vegf receptor vaccine demonstrates preliminary efficacy in neurofibromatosis type 2
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917794/
https://www.ncbi.nlm.nih.gov/pubmed/31848332
http://dx.doi.org/10.1038/s41467-019-13640-1
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