| Literature DB >> 33580079 |
Hiroki Takeuchi1, Keiko Imamura1,2,3, Bin Ji4, Kayoko Tsukita1,2, Takako Enami1,3, Keizo Takao5,6, Tsuyoshi Miyakawa7, Masato Hasegawa8, Naruhiko Sahara4, Nobuhisa Iwata9, Makoto Inoue10, Hideo Hara11, Takeshi Tabira12, Maiko Ono4, John Q Trojanowski13, Virginia M-Y Lee13, Ryosuke Takahashi14, Tetsuya Suhara4, Makoto Higuchi15, Haruhisa Inoue16,17,18.
Abstract
Pathological aggregates of tau proteins accumulate in the brains of neurodegenerative tauopathies including Alzheimer's disease and frontotemporal lobar degeneration (FTLD-tau). Although immunotherapies of these disorders against tau are emerging, it is unknown whether nasal delivery, which offers many benefits over traditional approaches to vaccine administration, is effective or not for tauopathy. Here, we developed vaccination against a secreted form of pathological tau linked to FTLD-tau using a Sendai virus (SeV) vector infectious to host nasal mucosa, a key part of the immune system. Tau vaccines given as nasal drops induced tissue tau-immunoreactive antibody production and ameliorated cognitive impairment in FTLD-tau model mice. In vivo imaging and postmortem neuropathological assays demonstrated the suppression of phosphorylated tau accumulation, neurotoxic gliosis, and neuronal loss in the hippocampus of immunized mice. These findings suggest that nasal vaccine delivery may provide a therapeutic opportunity for a broad range of populations with human tauopathy.Year: 2020 PMID: 33580079 DOI: 10.1038/s41541-020-0172-y
Source DB: PubMed Journal: NPJ Vaccines ISSN: 2059-0105 Impact factor: 7.344