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公开(公告)号:US10479998B2
公开(公告)日:2019-11-19
申请号:US15838556
申请日:2017-12-12
Applicant: Texas Tech University System
Inventor: Mingtao Zeng , Maria T. Arevalo
IPC: C07K16/28 , C12N15/11 , C12N15/113
Abstract: The present invention includes siRNAs and antibodies that block the interaction between TEM8 and/or CMG2 cell surface proteins and anthrax toxin and methods of treating anthrax exposure with the same.
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公开(公告)号:US20210236622A1
公开(公告)日:2021-08-05
申请号:US17048714
申请日:2019-04-18
Applicant: Texas Tech University System
Inventor: Mingtao Zeng , Ke Wen
IPC: A61K39/145 , A61K39/39 , C12N7/00 , C12N15/113
Abstract: The present invention includes a live, self-attenuated therapeutic vaccine, virus and methods of making and using the same, comprising: an isolated virus comprising a viral genome that expresses one or more viral antigens; and an artificial microRNA 30 (amiR-30) expression cassette inserted into a viral neuraminidase (NA) or a viral non-structural (NS) gene segment that expresses an amiR-30 that specifically inhibits the expression of a host gene essential for influenza virus replication in host cells.
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公开(公告)号:US20180112223A1
公开(公告)日:2018-04-26
申请号:US15838556
申请日:2017-12-12
Applicant: Texas Tech University System
Inventor: Mingtao Zeng , Maria T. Arevalo
IPC: C12N15/113 , C07K16/28
CPC classification number: C12N15/1138 , C07K16/28 , C07K2317/34 , C07K2317/76 , C12N2310/14 , C12N2320/30
Abstract: The present invention includes siRNAs and antibodies that block the interaction between TEM8 and/or CMG2 cell surface proteins and anthrax toxin and methods of treating anthrax exposure with the same.
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公开(公告)号:US20160145627A1
公开(公告)日:2016-05-26
申请号:US14898179
申请日:2014-06-12
Applicant: TEXAS TECH UNIVERSITY SYSTEM
Inventor: Mingtao Zeng , Maria T. Arevalo
IPC: C12N15/113 , C07K16/28
CPC classification number: C12N15/1138 , C07K16/28 , C07K2317/34 , C07K2317/76 , C12N2310/14 , C12N2320/30
Abstract: The present invention includes siRNAs and antibodies that block the interaction between TEM8 and/or CMG2 cell surface proteins and anthrax toxin and methods of treating anthrax exposure with the same.
Abstract translation: 本发明包括阻断TEM8和/或CMG2细胞表面蛋白质和炭疽毒素之间的相互作用的siRNA和抗体以及用其处理炭疽暴露的方法。
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公开(公告)号:US10370416B2
公开(公告)日:2019-08-06
申请号:US15446315
申请日:2017-03-01
Applicant: Texas Tech University System
Inventor: Mingtao Zeng , Maria T. Arevalo , Junwei Li
IPC: C07K14/005 , G01N33/50 , A61K39/07 , A61K39/12 , A61K39/00
Abstract: The present invention includes antigenic fusion proteins, nucleic acids encoding the fusion proteins and methods of making and using the same, wherein the fusion protein comprises three or more different influenza A ectodomains of Matrix Protein 2 (M2e); one or more stem regions of an influenza A hemagglutinin 2 (HA2) protein; and optionally an anthrax antigen, wherein the fusion protein is immunogenic across strains.
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公开(公告)号:US20180187191A1
公开(公告)日:2018-07-05
申请号:US15736358
申请日:2016-06-15
Applicant: Texas Tech University System
Inventor: Mingtao Zeng
IPC: C12N15/113 , A61P31/04 , A61K47/64
CPC classification number: C12N15/113 , A61K31/7105 , A61K35/742 , A61K38/164 , A61K47/6415 , A61P31/04 , C12N2310/14 , A61K2300/00
Abstract: The present invention includes a composition for the targeted-delivery of small interference RNA against bacteria comprising: a detoxified bacterial protein toxin that comprises a highly positively charged region; and an siRNA that is specific to, and knocks-down expression of one or more genes related to one or more virulence factors of the bacteria, wherein the siRNA is bound to the highly positively charged region of the detoxified bacterial protein toxin.
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公开(公告)号:US09862951B2
公开(公告)日:2018-01-09
申请号:US14898179
申请日:2014-06-12
Applicant: Texas Tech University System
Inventor: Mingtao Zeng , Maria T. Arevalo
IPC: C12N15/113 , C07K16/28
CPC classification number: C12N15/1138 , C07K16/28 , C07K2317/34 , C07K2317/76 , C12N2310/14 , C12N2320/30
Abstract: The present invention includes siRNAs and antibodies that block the interaction between TEM8 and/or CMG2 cell surface proteins and anthrax toxin and methods of treating anthrax exposure with the same.
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公开(公告)号:US20170253636A1
公开(公告)日:2017-09-07
申请号:US15446315
申请日:2017-03-01
Applicant: Texas Tech University System
Inventor: Mingtao Zeng , Maria T. Arevalo , Junwei Li
IPC: C07K14/005 , G01N33/50 , A61K39/145
CPC classification number: C07K14/005 , A61K39/07 , A61K39/12 , A61K2039/543 , A61K2039/572 , A61K2039/575 , A61K2039/70 , C07K2319/40 , C07K2319/55 , C12N2760/16122 , C12N2760/16134 , C12N2760/16143 , C12N2760/16162 , G01N33/5023 , G01N33/5088 , G01N2333/11 , G01N2333/32
Abstract: The present invention includes antigenic fusion proteins, nucleic acids encoding the fusion proteins and methods of making and using the same, wherein the fusion protein comprises three or more different influenza A ectodomains of Matrix Protein 2 (M2e); one or more stem regions of an influenza A hemagglutinin 2 (HA2) protein; and optionally an anthrax antigen, wherein the fusion protein is immunogenic across strains.
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公开(公告)号:US11946047B2
公开(公告)日:2024-04-02
申请号:US16660986
申请日:2019-10-23
Applicant: Texas Tech University System
Inventor: Mingtao Zeng , Lihong Wu
IPC: C12N15/113
CPC classification number: C12N15/113 , C12N2310/14 , C12N2320/32
Abstract: The present invention includes a composition and method for decreasing Bacillus anthracis virulence or toxicity comprising: at least one inhibitor that decreases an expression of one or more host genes selected from G6pc, Rgs1, Fosl2, Hcar2, Cxcl2 and Cxcl3, or Serpine1 (PAI-1).
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公开(公告)号:US10286062B2
公开(公告)日:2019-05-14
申请号:US14903611
申请日:2014-07-09
Applicant: Texas Tech University System
Inventor: Mingtao Zeng , Junwei Li
IPC: A61K39/145 , A61K39/12 , A61K39/39 , C12N7/00 , G01N33/569 , A61K39/00
Abstract: The present invention includes an isolated antigen against influenza A and a method of making the same that includes an ectodomain of influenza A Matrix Protein 2 (M2e) and a stem region of an influenza A hemagglutinin 2 (HA2) protein and an adjuvant. The invention further includes formulating the antigen into an isolated immune response stimulating fusion protein and/or a vaccine.
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