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公开(公告)号:US20220072045A1
公开(公告)日:2022-03-10
申请号:US17525802
申请日:2021-11-12
申请人: NantCell , Nant Holdings IP, LLC
发明人: Shahrooz Rabizadeh , Kayvan Niazi , Patrick Soon-Shiong , Hing Wong , Wenxin Xu
IPC分类号: A61K35/17 , A61K31/675 , C07K14/52 , C12N15/86
摘要: Contemplated treatments and methods produce substantially increased quantities of memory T-cells and a persistent immune response by subcutaneous and/or subdermal co-administration of (1) a vector comprising a recombinant nucleic acid that encodes a cancer associated epitope, a cancer specific epitope, and/or a neoepitope, (2) an immune stimulating cytokine, and (3) a checkpoint inhibitor. Most typically, the co-administration is performed at substantially the same location, preferably within 1-21 days from each other, and the vector is an adenoviral expression vector, for example, included in a viral particle such as an AdV5 virus with a deletion of the E2b gene.
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公开(公告)号:US11071774B2
公开(公告)日:2021-07-27
申请号:US16783734
申请日:2020-02-06
发明人: Patrick Soon-Shiong , Kayvan Niazi , Shahrooz Rabizadeh , Hans G. Klingemann , Laurent H. Boissel
摘要: Cancer is treated using coordinated treatment regimens that uses various compounds and compositions that drive a tumor from the escape phase of cancer immunoediting to the elimination and equilibrium phase of cancer immunoediting.
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公开(公告)号:US20210198689A1
公开(公告)日:2021-07-01
申请号:US16081014
申请日:2017-03-20
IPC分类号: C12N15/86 , C07K14/705
摘要: Recombinant viruses and viral nucleic acids are contemplated that provide to the infected cell various regulatory molecules that stimulate T-cell and NK-cell activity and that suppress inhibition of T-cell and NK-cell activity. Most preferably, the virus and viral nucleic acid will further include a human cancer-associated sequence, and especially a sequence that encodes a plurality of cancer associated antigens, cancer specific antigens, and/or patient and tumor specific neoantigens. Especially preferred regulatory molecules include CD80 (B7.1), CD86 (B7.2), CD54 (ICAM-1/BB2), CD11 (LFA-1), and an inhibitor of CTLA-4.
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公开(公告)号:US10793875B2
公开(公告)日:2020-10-06
申请号:US16060020
申请日:2016-12-07
IPC分类号: C12N15/86 , A61K38/20 , A61K39/00 , A61K38/19 , A61K35/761
摘要: Cancer immunotherapy is enhanced by co-expression of cancer associated or tumor-specific (neo)epitopes with co-stimulatory molecules and/or other immune activators. Where desired, treatment may be enhanced by administration of a immune checkpoint inhibitor.
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公开(公告)号:US20200291432A1
公开(公告)日:2020-09-17
申请号:US16836515
申请日:2020-03-31
IPC分类号: C12N15/86 , A61K39/00 , A61K38/19 , A61K38/20 , A61K35/761
摘要: Cancer immunotherapy is enhanced by co-expression of cancer associated or tumor-specific (neo)epitopes with co-stimulatory molecules and/or other immune activators. Where desired, treatment may be enhanced by administration of a immune checkpoint inhibitor.
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公开(公告)号:US20190167722A1
公开(公告)日:2019-06-06
申请号:US16322310
申请日:2017-08-02
发明人: Patrick Soon-Shiong , Kayvan Niazi
IPC分类号: A61K35/17 , C12N5/0783 , A61K35/15 , A61K38/20 , A61K39/00 , C12N5/0781 , C12N5/0784
摘要: Immunotherapeutic methods and compositions are contemplated where one or more neoepitopes and/or tumor associated antigens are produced in, or delivered to dendritic cells, and in which so modified dendritic cells are co-cultured with immune competent cells of a patient, preferably in the presence of stimulatory signals. Cells are then transfused to the patient that has preferably undergone immune checkpoint inhibition treatment.
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公开(公告)号:US20190091316A1
公开(公告)日:2019-03-28
申请号:US16075874
申请日:2017-02-12
摘要: Immunotherapeutic methods and compositions are contemplated in which neoepitopes and/or tumor associated antigens are delivered to dendritic cells via an adenoviral expression system that targets MHC-I and/or MHC-II presentation systems and that further provides one or more recombinant peptides to stimulate T cell activation and interfere with checkpoint inhibition. Treatment is further supported by transfusion of NK cells, which may be modified to have a high affinity CD 16 receptor and/or a chimeric antigen receptor that binds to one or more neoepitopes and/or tumor associated antigens.
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公开(公告)号:US20190046570A1
公开(公告)日:2019-02-14
申请号:US16073947
申请日:2017-02-03
IPC分类号: A61K35/17 , C12N15/85 , C12N15/11 , A61P35/00 , C07K14/705 , C12N5/0781 , C12N5/0783 , C12N5/0784 , A61K48/00
摘要: Recombinant expression of CXADR in a cell, and especially an immune competent cell is employed to enable or improve gene delivery to the cell by an adenovirus. In particularly preferred aspects, the immune competent cell is a an NK cell, a T-cell, a B-cell, a macrophage, or a dendritic cell, and the gene delivery comprises a recombinant nucleic acid encoding a disease-specific antigen, such as a patient specific neoepitope or a tumor associated antigen.
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公开(公告)号:US09987282B2
公开(公告)日:2018-06-05
申请号:US15213049
申请日:2016-07-18
发明人: Kayvan Niazi , Shahrooz Rabizadeh , Anne-Laure LeNy , Oleksandr Buzko , Justin Golovato , Patrick Soon-Shiong
IPC分类号: A61K31/519
CPC分类号: A61K31/519 , C07D487/04
摘要: Antiviral compositions and methods are contemplated that are especially effective in the treatment and prevention of influenza A viruses. Also presented are cellular assays to identify small molecule compounds having antiviral properties, particularly as it relates to detection of influenza A RNA-dependent RNA polymerase activity in a mammalian cell independent of other influenza A components. Preferred assays allow for identification of viral replication inhibitors that do not disrupt normal cellular activity.
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公开(公告)号:US20170128568A1
公开(公告)日:2017-05-11
申请号:US15264947
申请日:2016-09-14
发明人: Kayvan Niazi , Shahrooz Rabizadeh , Justin Golovato , Patrick Soon-Shiong , Anne-Laure Le Ny , Oleksandr Buzko
IPC分类号: A61K39/39 , A61K39/085
CPC分类号: A61K39/39 , A61K9/0014 , A61K31/05 , A61K31/12 , A61K31/16 , A61K31/341 , A61K31/365 , A61K31/404 , A61K31/407 , A61K31/423 , A61K31/66 , A61K33/24 , A61K39/085 , A61K47/06 , A61K47/10 , A61K2039/54 , A61K2039/55511 , A61K2039/57
摘要: Calcium flux agonists are used to enhance a TLR- or NOD-mediated stimulus and to so increase an immune response of a host and reduce healing time. Preferred calcium flux agonists include Ca2+ ionophores and SERCA inhibitors and are used in synergistic quantities where a ligand to a TLR or NOD receptor is present.
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