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公开(公告)号:US20240182858A1
公开(公告)日:2024-06-06
申请号:US18282450
申请日:2022-03-16
发明人: Kenichiro SHIMATANI , Hiromu SATO , Masao SASAI , Yoshiki SAWA , Atsuhiro SAITO , Shigeru MIYAGAWA
CPC分类号: C12N5/0661 , A61K35/44 , A61P7/00 , C07K14/503 , C12N5/10
摘要: An object of the present invention is to provide a cell therapy that is expected to be useful as an angiogenic therapy for a peripheral vascular disease such as critical lower limb ischemia. Specifically, the object is to provide a pericyte having high angiogenic potential and a method for producing the same. A pericyte introduced a bFGF gene and a method for producing the same are provided.
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公开(公告)号:US20240316115A1
公开(公告)日:2024-09-26
申请号:US18579093
申请日:2022-07-14
发明人: Kenichiro SHIMATANI , Hiromu SATO , Masao SASAI , Yoshiki SAWA , Atsuhiro SAITO , Shigeru MIYAGAWA
CPC分类号: A61K35/44 , C12N5/069 , C12N2500/32 , C12N2500/90 , C12N2501/115 , C12N2501/135 , C12N2506/02 , C12N2509/00 , C12N2513/00 , C12N2533/52 , C12N2533/54
摘要: An object of the present invention is to provide a pericyte-like cell having high angiogenic potential with a higher cell proliferation ability than a primary pericyte available in the past and high VEGF expression, and a method for producing the same. Provided are a method for producing a VEGF-highly expressing pericyte-like cell, the method including selecting a CD56(−) pericyte-like cell from a population including a pericyte-like cell obtained by inducing differentiation of a pluripotent stem cell; and a VEGF-highly expressing pericyte-like cell produced by the production method.
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公开(公告)号:US20240335480A1
公开(公告)日:2024-10-10
申请号:US18579100
申请日:2022-07-14
发明人: Kenichiro SHIMATANI , Hiromu SATO , Masao SASAI , Yoshiki SAWA , Atsuhiro SAITO , Shigeru MIYAGAWA
IPC分类号: A61K35/545 , A61K35/44 , C12N5/071
CPC分类号: A61K35/545 , A61K35/44 , C12N5/069 , C12N2506/02 , C12N2513/00
摘要: An object of the present invention is to provide a pericyte-like cell having high angiogenic potential with a higher cell proliferation ability than a primary pericyte available in the past and high VEGF expression, and a method for producing the same. Provided are a method for producing a VEGF-highly expressing pericyte-like cell, the method including selecting a CD56(−) pericyte-like cell from a population including a pericyte-like cell obtained by inducing differentiation of a pluripotent stem cell; and a VEGF-highly expressing pericyte-like cell produced by the production method.
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公开(公告)号:US20160046720A1
公开(公告)日:2016-02-18
申请号:US14927007
申请日:2015-10-29
申请人: Astellas Pharma Inc.
发明人: Hiromu SATO , Daisuke Yamajuku , Kazunori Arai , Mako Ogino
IPC分类号: C07K16/28
CPC分类号: C07K16/2866 , A61K2039/505 , C07K14/715 , C07K16/244 , C07K2317/21 , C07K2317/24 , C07K2317/40 , C07K2317/565 , C07K2317/76 , C07K2317/92 , C07K2319/30 , C12P21/02
摘要: [Problem] To provide an anti-human TSLP receptor antibody that specifically binds to human TSLP receptor and inhibits an action of human TSLP through human TSLP receptor.[Means for Solution] An anti-human TSLP receptor antibody had been studied by the present inventors, and an anti-human TSLP receptor antibody comprising a heavy chain variable region consisting of the amino acid sequence of amino acid numbers 1 to 118 of SEQ ID NO: 1 and a light chain variable region consisting of the amino acid sequence of amino acid numbers 1 to 108 of SEQ ID NO: 3 was provided. It was revealed that the anti-human TSLP receptor antibody inhibits expression of TARC mRNA induced by TSLP and production of MDC proteins, and suppressed an allergic reaction in a monkey Ascaris antigen sensitization model, and then the present invention was completed.
摘要翻译: [问题]提供与人TSLP受体特异性结合并通过人TSLP受体抑制人TSLP的作用的抗人TSLP受体抗体。 [解决方案]本发明人研究了抗人TSLP受体抗体,抗人TSLP受体抗体包含由SEQ ID NO:1的氨基酸序列1〜118的氨基酸序列构成的重链可变区 提供由SEQ ID NO:3的氨基酸序列号1至108组成的轻链可变区。 显示抗人TSLP受体抗体抑制由TSLP诱导的TARC mRNA的表达和MDC蛋白的产生,并抑制猴蛔虫抗原致敏模型中的过敏反应,然后完成本发明。
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公开(公告)号:US20160208005A1
公开(公告)日:2016-07-21
申请号:US15090051
申请日:2016-04-04
申请人: Astellas Pharma Inc.
发明人: Hiromu SATO , Daisuke Yamajuku , Kazunori Arai , Mako Ogino
IPC分类号: C07K16/28
CPC分类号: C07K16/2866 , A61K2039/505 , C07K14/715 , C07K16/244 , C07K2317/21 , C07K2317/24 , C07K2317/40 , C07K2317/565 , C07K2317/76 , C07K2317/92 , C07K2319/30 , C12P21/02
摘要: An anti-human TSLP receptor antibody that specifically binds to human TSLP receptor and inhibits an action of human TSLP through human TSLP receptor. A method for preventing or treating asthma by administering the anti-human TSLP receptor antibody or an antigen-binding fragment thereof. An anti-human TSLP receptor antibody had been studied by the present inventors, and an anti-human TSLP receptor antibody including a heavy chain variable region consisting of the amino acid sequence of amino acid numbers 1 to 118 of SEQ ID NO: 1 and a light chain variable region consisting of the amino acid sequence of amino acid numbers 1 to 108 of SEQ ID NO: 3 was provided. It was revealed that the anti-human TSLP receptor antibody inhibits expression of TARC mRNA induced by TSLP and production of MDC proteins, and suppressed an allergic reaction in a monkey Ascaris antigen sensitization model.
摘要翻译: 特异性结合人TSLP受体并通过人TSLP受体抑制人TSLP的作用的抗人TSLP受体抗体。 通过施用抗人TSLP受体抗体或其抗原结合片段来预防或治疗哮喘的方法。 本发明人研究了抗人TSLP受体抗体,包含由SEQ ID NO:1的氨基酸序列1〜118的氨基酸序列构成的重链可变区的抗人TSLP受体抗体和 提供了由SEQ ID NO:3的氨基酸编号1至108的氨基酸序列组成的轻链可变区。 显示抗人TSLP受体抗体抑制由TSLP诱导的TARC mRNA的表达和MDC蛋白的产生,并抑制猴蛔虫抗原致敏模型中的过敏反应。
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