A VEGF receptor vaccine demonstrates preliminary efficacy in neurofibromatosis type 2.
Masahiro TodaMasato FujiokaYukina MorimotoKentaro OharaKenzo KosugiYumiko OishiMizuto SatoRyo UedaHirokazu FujiwaraTetsuro HikichiShinobu NojiNaoki OishiKaoru OgawaYutaka KawakamiTakayuki OhiraKazunari YoshidaMasahiro TodaPublished in: Nature communications (2019)
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.
Keyphrases
- end stage renal disease
- vascular endothelial growth factor
- newly diagnosed
- chronic kidney disease
- ejection fraction
- prognostic factors
- signaling pathway
- multiple sclerosis
- patient reported outcomes
- poor prognosis
- inflammatory response
- toll like receptor
- cell death
- long non coding rna
- high glucose
- replacement therapy
- diabetic rats
- coronary artery bypass