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公开(公告)号:US20180280444A1
公开(公告)日:2018-10-04
申请号:US15619021
申请日:2017-06-09
申请人: Batu Biologics, Inc.
发明人: Samuel C. Wagner , Thomas E. Ichim
IPC分类号: A61K35/44 , A61K39/00 , A61K31/235
摘要: Disclosed are methods, compositions of matter, and therapeutic protocols for treatment of cancer by selectively inducing immune responses against blood vessels feeding neoplastic tissue. In one embodiment, placental endothelial cells are stimulated with Phorbol Myristate Acetate (PMA) to induce release of nanoparticles that possess ability to: a) be taken up by antigen presenting; b) presented through direct and indirect presentation to CD4 and CD8 T cells, respectively; and c) utilized to stimulate cytoxic T cellular and humoral responses to selectively inhibit angiogenesis of tumors.
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公开(公告)号:US20170151281A1
公开(公告)日:2017-06-01
申请号:US15048922
申请日:2016-02-19
申请人: Batu Biologics, Inc.
发明人: Samuel C. Wagner , Thomas E. Ichim , Julia S. Szymanski , Santosh Kesari , Amit N. Patel , Boris Minev
IPC分类号: A61K35/15 , A61K39/395 , A61K38/17 , C12N5/0786
CPC分类号: A61K35/15 , A61K38/177 , C07K16/00 , C07K16/30 , C07K16/32 , C07K2317/622 , C07K2319/03 , C07K2319/33 , C12N5/0645 , C12N2501/599 , C12N2510/00
摘要: The current invention provides monocytic cells transfected with chimeric antigen receptor (CAR) to selectively home to tumors and upon homing differentiate into dendritic cells capable of activating immunity which is inhibitory to said tumor. In one embodiment of the invention, monocytic cells are transfected with a construct encoding an antigen binding domain, a transcellular or structural domain, and an intracellular signaling domain. In one specific aspect of the invention, the antigen binding domain interacts with sufficient affinity to a tumor antigen, capable of triggering said intracellular domain to induce an activation signal to induce monocyte differentiation into DC.
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公开(公告)号:US20170100438A1
公开(公告)日:2017-04-13
申请号:US15288493
申请日:2016-10-07
申请人: Batu Biologics, Inc.
CPC分类号: C12N5/069 , A61K35/44 , C12N2506/025
摘要: Disclosed are compositions of matter, therapeutic protocols, and immunization means to induce an active immune response to vasculature feeding glioma or other brain neoplasia. In one embodiment the invention provides administration of placental derived endothelial cells at concentrations of 10 million to 50 million administered in a manner to stimulate immunity toward blood vessels supplying glioma or other brain neoplastic malignancies. The invention provides means of blocking augmenting efficacy of immunotherapy, chemotherapy, and radiotherapy.
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公开(公告)号:US20200297829A1
公开(公告)日:2020-09-24
申请号:US16356892
申请日:2019-03-18
申请人: BATU BIOLOGICS, INC.
发明人: Samuel C. Wagner , Thomas E. Ichim
摘要: Disclosed are means, methods, and compositions of matter useful for treatment of cancer through integrated immunotherapy. In one embodiment a synergistic protocol is comprised of: a) establishing a proteomic, genomic, and immunological profile of the patient; b) stimulation of a change in the tumor microenvironment in order to modify the tumor microenvironment to be more conducive to immunotherapy; c) priming the immune system in order to be prepared for immune activation; d) activate vaccination in order to induce antigen specific immune responses; e) induction of damage to the tumor in an immunogenic manner; f) immune focusing by utilization of epitope specific vaccination; and g) boosting the immune response.
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公开(公告)号:US20190201511A1
公开(公告)日:2019-07-04
申请号:US16239346
申请日:2019-01-03
申请人: BATU BIOLOGICS, INC.
IPC分类号: A61K39/00
CPC分类号: A61K39/0006 , A61K2039/515 , A61K2039/55 , A61K2039/572 , A61K2039/575
摘要: Disclosed are methods of preventing pregnancy through induction of immunological responses through vaccination with placental extracts and products associated with placentation. In one particular embodiment an immune response is triggered towards pregnancy associated neoangiogenesis through administration of placental endothelial cells capable of triggering immunity. In other embodiments the process of replicating immunological events associated with pregnancy failure are recapitulated by stimulation of immunity to antigens such as VEGFR-1, VEGFR-2, CD105, FGF1-R, Integrin αvβ3, and CD-248.
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公开(公告)号:US20170348388A1
公开(公告)日:2017-12-07
申请号:US15611694
申请日:2017-06-01
申请人: Batu Biologics, Inc.
发明人: Samuel C. Wagner , Thomas E. Ichim
IPC分类号: A61K38/19 , A61K39/395 , A61K39/00 , A61K39/21 , A61K48/00
CPC分类号: A61K38/19 , A61K39/00 , A61K39/0011 , A61K39/395 , A61K47/646 , A61K48/00 , A61K2039/5152 , A61K2039/5156 , A61K2039/55522 , C07K16/00 , C07K2317/732 , C07K2317/75
摘要: Adjuvants acting at the level of antigen presentation useful for stimulation of specific immunity against tumor endothelial cells. In one embodiment the invention teaches the use of activation of specific antigen presenting cell programs to selectively induce cytotoxic T cells and antibodies with complement activating ability while not evoking antigenic responses that potentially stimulate angiogenesis or growth of tumor endothelial cells. Specifically, the invention teaches selection and use of adjuvants that inhibit suppressive dendritic cell produced factors, surface bound and soluble, while stimulating activatory cytokines. Adjuvant means include innate activatory molecules, gene silencing means, alarmins, and other stimulatory means resembling “danger” signals.
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公开(公告)号:US20170196951A1
公开(公告)日:2017-07-13
申请号:US15231759
申请日:2016-08-08
申请人: Batu Biologics, Inc.
发明人: Samuel C. Wagner , Thomas E. Ichim , Amit N. Patel
CPC分类号: A61K39/0011 , A61K35/33 , A61K2039/515 , A61K2039/5152 , C12N5/0656 , C12N15/85 , C12N2501/23 , C12N2501/2301 , C12N2501/2306 , C12N2501/2333 , C12N2501/24 , C12N2501/25 , C12N2502/1157 , C12N2502/30
摘要: Compositions of matter, of production, and treatment modalities are disclosed for the prevention and/or therapeutic reduction of tumors through induction of immunity against tumor associated fibroblasts and components of tumor microenvironment. In one embodiment of the invention, placentally derived fibroblast cells are cultured under conditions replicating tumor microenvironment. Expression of CD248 on said cultured fibroblasts is used as a marker of effective manipulation. Cells expressing CD248 are utilized a immunogens for stimulation of immunity towards cancer associated fibroblastic cells.
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公开(公告)号:US20170165332A1
公开(公告)日:2017-06-15
申请号:US15227772
申请日:2016-08-03
申请人: Batu Biologics, Inc.
发明人: Samuel C. Wagner , Thomas E. Ichim
IPC分类号: A61K39/00
CPC分类号: A61K39/0008 , A61K39/0011 , A61K2039/5154 , C12N5/0639 , C12N2510/00
摘要: Disclosed are cells, compositions of matter, and protocols, useful for stimulation of antigen-specific immunity or tolerogenesis by gene editing of immune suppressive costimulatory molecules for induction of immune stimulation, and gene editing of immune stimulatory molecules for immune suppression. Provided are means of stimulating immunity to cancer, viral antigens, or bacterial antigens through pulsing, fusing, or administering antigenic compositions to antigen presenting cells that are gene silenced for immune suppressive genes. Provided are means of treating transplant rejection or autoimmunity by gene silencing immune stimulatory genes.
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公开(公告)号:US20170107510A1
公开(公告)日:2017-04-20
申请号:US15293999
申请日:2016-10-14
申请人: Batu Biologics, Inc.
发明人: Samuel C. Wagner , Thomas E. Ichim
IPC分类号: C12N15/10 , C12N15/115
CPC分类号: C12N15/1093 , C12N15/111 , C12N15/115 , C12N2310/16
摘要: The invention discloses the utilization of DNA generated nanoparticles to block interaction between inhibitory signals in immune cells. Provided are compositions of matter, protocols and treatment methodologies for stimulation immunity through inhibiting suppressive molecules through the use of DNA based nanoparticles.
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公开(公告)号:US20190282641A1
公开(公告)日:2019-09-19
申请号:US16356803
申请日:2019-03-18
申请人: BATU BIOLOGICS, INC.
发明人: Samuel C. Wagner , Thomas E. Ichim
IPC分类号: A61K35/768 , C12N5/095 , C12N7/00 , A61K35/13 , A61K39/00
摘要: Disclosed are means, methods, and compositions of matter useful for generation of viruses that selectively grow in the tumor endothelium and causes lysis or augmentation of tumor immunity. In one embodiment an oncolytic virus is selectively maintained in cells resembling tumor endothelium under conditions allowing for the oncolytic virus to capture immunogenic entities found on the cells resembling tumor endothelial cells. In another embodiment, the endothelial cells resembling tumor endothelial cells are utilized as a “Trojan horse” for selective delivery of virus into a tumor or tumor microenvironment.
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