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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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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. |
format | Online Article Text |
id | pubmed-6917794 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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