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公开(公告)号:US20190083462A1
公开(公告)日:2019-03-21
申请号:US16085896
申请日:2017-03-17
Applicant: THE TEXAS A&M UNIVERSITY SYSTEM , TRUSTEES OF TUFTS COLLEGE
Inventor: Robert C. Alaniz , Arul Jayaraman , Kyongbum Lee , Canaan Whitfield , Noah Cohen
IPC: A61K31/405 , A61K45/06 , A61P1/00
Abstract: This disclosure relates to methods and compositions for addressing conditions of dysbiosis and/or inflammation, such as enteropathy, associated with administration of non-steroidal anti-inflammatory drug (NSAID). The disclosure includes methods comprising administering an effective amount of a tryptophan derived microbiota metabolite (TDMM) to a subject that has also been administered, or is expected to have administered, a NSAID.
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公开(公告)号:US20240189279A1
公开(公告)日:2024-06-13
申请号:US18536002
申请日:2023-12-11
Applicant: THE TEXAS A&M UNIVERSITY SYSTEM , TRUSTEES OF TUFTS COLLEGE
Inventor: Arul Jayaraman , Kyongbum Lee
IPC: A61K31/405 , A61K9/00 , A61K31/4045 , A61P1/16 , A61P11/00 , A61P31/14
CPC classification number: A61K31/405 , A61K9/0053 , A61K31/4045 , A61P1/16 , A61P11/00 , A61P31/14
Abstract: Provided here are immunomodulatory compositions for and methods of treatment of inflammation-associated diseases, such as liver disorders and acute respiratory distress syndrome (ARDS). The composition can be a tryptophan metabolite, such as indole 3-acetate, tryptamine, xanthurenic acid, or a derivative of any thereof. The methods can include administering the subject a therapeutically effective amount of the immunomodulatory composition provided herein. The liver disorders can be non-alcoholic fatty liver disease, steatosis, non-alcoholic steatohepatitis, and/or fibrosis. The ARDS can be associated with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection.
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公开(公告)号:US20200217778A1
公开(公告)日:2020-07-09
申请号:US16607787
申请日:2018-04-30
Applicant: The Texas A&M University System
Inventor: Susmitha Purnima Kotu , Arul Jayaraman , Mahboobul Sam Mannan , Arum Han
Abstract: A method for determining the susceptibility of a material to corrosion includes generating, via an inlet in a monitoring device, a laminar flow of material comprising a plurality of microorganisms. The plurality of microorganisms comprises at least one microorganism type. The method also includes forming, inside the monitoring device, in response to the laminar flow, a biofilm comprising at least one microorganism type. In addition, the method includes applying a voltage to the first and second electrodes during the laminar flow.
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公开(公告)号:US11612586B2
公开(公告)日:2023-03-28
申请号:US16085912
申请日:2017-03-17
Applicant: THE TEXAS A&M UNIVERSITY SYSTEM , TRUSTEES OF TUFTS COLLEGE
Inventor: Robert C. Alaniz , Arul Jayaraman , Kyongbum Lee
IPC: A61K31/405 , A61K31/404 , A61K31/475 , A61K35/17 , A61K45/06 , A61P1/00 , A61P29/00 , C12N5/0783 , C12N5/0784 , A61K35/12 , A61K31/7004
Abstract: The disclosure provides methods and compositions for affecting the development of antigen presenting cell (APC, e.g., a macrophage or dendritic cell). The methods include maturing an APC, promoting anti-inflammatory phenotype, promoting development of a T regulatory cell (Treg) from a naive T cell. The methods generally include exposing an APC to a tryptophan derived microbiota metabolite (TDMM), such as an anti-inflammatory or pro-mucosal TDMM, and permitting the APC to mature. In some embodiments, the conditioned APC is exposed to a naive T cell to further promote development of a T regulatory cell (Treg). In some embodiments, the TDMM is selected from the group consisting of indole, indole-3-acetate, 5-hydroxyindole, and indole-3-pyruvate.
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5.
公开(公告)号:US20190032014A1
公开(公告)日:2019-01-31
申请号:US16085926
申请日:2017-03-17
Applicant: THE TEXAS A&M UNIVERSITY SYSTEM , TRUSTEES OF TUFTS COLLEGE
Inventor: Robert C. Alaniz , Arul Jayaraman , Kyongbum Lee
IPC: C12N5/0783 , A61K31/405 , A61K35/17 , A61K31/475 , A61P29/00
Abstract: Disclosed are compositions derived from the commensal microbiota and related methods for inducing and differentiating naive T cells. In some embodiments, the compositions and methods can be selectively used to generate stable regulatory T-cells (Tregs or iTregs) or stabilize such Tregs to prevent inflammatory responses and instead promote antigen tolerance. Alternatively, in other aspects, select compositions can be used to promote pro-inflammatory T cell development, such as through the induced development and stabilization of Th1 and Th7 cells.
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