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論文
タイトル
タイトル(英)
First-in-human clinical trial of the NKT cell-stimulatory glycolipid OCH in multiple sclerosis.
参照URL
https://researchmap.jp/kimura_vision/published_papers/43691836
著者
著者(英)
Wakiro Sato,Daisuke Noto,Manabu Araki,Tomoko Okamoto,Youwei Lin,Hiromi Yamaguchi,Ryoko Kadowaki-Saga,Atsuko Kimura,Yukio Kimura,Noriko Sato,Takami Ishizuka,Harumasa Nakamura,Sachiko Miyake,Takashi Yamamura
担当区分
概要
概要(英)
BACKGROUND: Multiple sclerosis (MS) is an autoimmune inflammatory disease of the central nervous system that causes the damage to the myelin sheath as well as axonal degeneration. Individuals with MS appear to have changes in the numbers and functions of T-cell subsets, leading to an immunological imbalance accompanied by enhanced autoreactivity. In previous preclinical studies, (2 S,3 S,4R)-1-O-(α-D-Galactopyranosyl)-N-tetracosanoyl-2-amino-1,3,4-nonanetriol (OCH), a synthetic analog of α-galactosylceramide stimulatory for invariant NKT (iNKT) cells, has shown therapeutic or disease-preventive immunoregulatory effects in autoimmune disease models such as experimental autoimmune encephalomyelitis (EAE). OBJECTIVES: This study is the first-in-human study of oral OCH to evaluate the pharmacokinetics and to examine the effects on immune cells as well as related gene expression profiles. METHODS: Fifteen healthy volunteers and 13 MS patients who met the study criteria were enrolled. They were divided into five cohorts and received oral administration of various doses of granulated powder of OCH (0.3-30 mg), once per week for 4 or 13 weeks. Plasma OCH concentrations were measured by high-performance liquid chromatography. Frequencies of lymphocyte subsets in peripheral blood were evaluated by flow cytometry, and microarray analysis was performed to determine OCH-induced changes in gene expression. RESULTS: Oral OCH was well tolerated, and its bioavailability was found to be sufficient. Six hours after a single dose of OCH, increased frequencies of Foxp3+ regulatory T-cells were observed in some cohorts of healthy subjects and MS patients. Furthermore, gene expression analysis demonstrated an upregulation of several immunoregulatory genes and downregulation of pro-inflammatory genes following OCH administration. CONCLUSION: This study has demonstrated immunomodulatory effects of the iNKT cell-stimulatory drug OCH in human. Safety profiles together with the presumed anti-inflammatory effects of oral OCH encouraged us to conduct a phase II trial.
出版者・発行元
出版者・発行元(英)
誌名
誌名(英)
Therapeutic advances in neurological disorders
16
開始ページ
17562864231162153
終了ページ
17562864231162153
出版年月
2023年
査読の有無
招待の有無
掲載種別
研究論文(学術雑誌)
ISSN
DOI URL
https://doi.org/10.1177/17562864231162153
共同研究・競争的資金等の研究課題
研究者