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1.
公开(公告)号:EP2929893A1
公开(公告)日:2015-10-14
申请号:EP13860873.2
申请日:2013-11-15
Applicant: Daiichi Sankyo Company, Limited , Osaka University
Inventor: FUJINAGA, Yukako , MATSUMURA, Takuhiro , YUTANI, Masahiro , JONAI, Nao
CPC classification number: A61K39/39 , A61K39/00 , A61K39/02 , A61K39/12 , A61K39/145 , A61K2039/5252 , A61K2039/541 , A61K2039/543 , A61K2039/55516 , A61K2039/55544 , A61K2039/575 , C07K14/33 , C07K14/77 , C07K2319/42 , C12N7/00 , C12N2760/16134 , Y02A50/386 , Y02A50/39 , Y02A50/466 , Y02A50/472
Abstract: An object of the present invention is to provide an adjuvant for a mucosal vaccine with high safety that induces a sufficient immune response on the mucosa. According to the present invention, an adjuvant for a mucosal vaccine comprising a protein complex composed of hemagglutinin (HA) subcomponents HA1, HA2, and HA3 of botulinum toxin is provided.
Abstract translation: 本发明的目的是提供一种具有高安全性的粘膜疫苗佐剂,其在粘膜上诱导足够的免疫应答。 根据本发明,提供了一种包含由肉毒杆菌毒素的血凝素(HA),亚组分HA1,HA2和HA3组成的蛋白质复合物的粘膜疫苗佐剂。
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2.
公开(公告)号:EP4477744A1
公开(公告)日:2024-12-18
申请号:EP23749881.1
申请日:2023-02-06
Applicant: OSAKA UNIVERSITY
Inventor: KINOOKA, Masahiro , KIM, Meehae , FUJINAGA, Yukako
Abstract: A method for producing a retinal pigment epithelial (RPE) cell, including promoting differentiation induction from a pluripotent stem cell into an RPE cell by culturing the pluripotent stem cell in a medium containing an E-cadherin inhibitor is provided by the present invention.
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3.
公开(公告)号:EP4477743A1
公开(公告)日:2024-12-18
申请号:EP23749882.9
申请日:2023-02-06
Applicant: OSAKA UNIVERSITY
Inventor: KINOOKA, Masahiro , KIM, Meehae , FUJINAGA, Yukako
IPC: C12N5/02 , C12N5/0735 , C12N5/10
Abstract: The present invention provides an agent for directional control of differentiation induction of a pluripotent stem cell, comprising an E-cadherin inhibitor.
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公开(公告)号:EP3715378A1
公开(公告)日:2020-09-30
申请号:EP18880123.7
申请日:2018-11-22
Inventor: FUJINAGA, Yukako , AMATSU, Sho , KINOOKA, Masahiro
Abstract: The present invention provides a miniaturized hemagglutinin complex protein having function inhibitory activity against E-cadherin, wherein
(a) all or a part of at least HA1 subcomponent, and/or a part of HA3 subcomponent are/is deleted,
(b) regions in HA2 and HA3 subcomponents that contribute to binding with E-cadherin are present, and
(c) the HA3 subcomponent is derived from Clostridium botulinum type A or type B, and an E-cadherin function inhibitor containing the hemagglutinin complex protein.
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