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Oral encapsulated transforming growth factor β1 reduces endogenous levels: Effect on inflammatory bowel disease

BACKGROUND: TreXTAM(® )is a combination of the key regulatory cytokine transforming growth factor beta (TGFβ) and all trans retinoic acid (ATRA) microencapsulated for oral delivery to immune structures of the gut. It is in development as a novel treatment for inflammatory bowel disease (IBD). AIM: T...

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Autores principales: Hammer, Laura, Furtado, Stacia, Mathiowitz, Edith, Auci, Dominick L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667406/
https://www.ncbi.nlm.nih.gov/pubmed/33251033
http://dx.doi.org/10.4292/wjgpt.v11.i5.79
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author Hammer, Laura
Furtado, Stacia
Mathiowitz, Edith
Auci, Dominick L
author_facet Hammer, Laura
Furtado, Stacia
Mathiowitz, Edith
Auci, Dominick L
author_sort Hammer, Laura
collection PubMed
description BACKGROUND: TreXTAM(® )is a combination of the key regulatory cytokine transforming growth factor beta (TGFβ) and all trans retinoic acid (ATRA) microencapsulated for oral delivery to immune structures of the gut. It is in development as a novel treatment for inflammatory bowel disease (IBD). AIM: To measure TGFβ levels in blood and tissue after oral administration of encapsulated TGFβ. METHODS: Animals were orally administered encapsulated TGFβ by gavage. Levels of drug substance in blood and in gut tissues at various times after administration were measured by ELISA. RESULTS: We made the surprising discovery that oral administration of TreXTAM dramatically (approximately 50%) and significantly (P = 0.025) reduced TGFβ levels in colon, but not small intestine or mesenteric lymph nodes. Similarly, levels in rat serum after 25 d of thrice weekly dosing with either TreXTAM, or microencapsulated TGFβ alone (denoted as TPX6001) were significantly (P < 0.01) reduced from baseline levels. When tested in the SCID mouse CD4+CD25- adoptive cell transfer (ACT) model of IBD, oral TPX6001 alone provided only a transient benefit in terms of reduced weight loss. CONCLUSION: These observations suggest a negative feedback mechanism in the gut whereby local delivery of TGFβ results in reduced local and systemic levels of the active form of TGFβ. Our findings suggest potential clinical implications for use of encapsulated TGFβ, perhaps in the context of IBD and/or other instances of fibrosis and/or pathological TGFβ signaling.
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spelling pubmed-76674062020-11-27 Oral encapsulated transforming growth factor β1 reduces endogenous levels: Effect on inflammatory bowel disease Hammer, Laura Furtado, Stacia Mathiowitz, Edith Auci, Dominick L World J Gastrointest Pharmacol Ther Basic Study BACKGROUND: TreXTAM(® )is a combination of the key regulatory cytokine transforming growth factor beta (TGFβ) and all trans retinoic acid (ATRA) microencapsulated for oral delivery to immune structures of the gut. It is in development as a novel treatment for inflammatory bowel disease (IBD). AIM: To measure TGFβ levels in blood and tissue after oral administration of encapsulated TGFβ. METHODS: Animals were orally administered encapsulated TGFβ by gavage. Levels of drug substance in blood and in gut tissues at various times after administration were measured by ELISA. RESULTS: We made the surprising discovery that oral administration of TreXTAM dramatically (approximately 50%) and significantly (P = 0.025) reduced TGFβ levels in colon, but not small intestine or mesenteric lymph nodes. Similarly, levels in rat serum after 25 d of thrice weekly dosing with either TreXTAM, or microencapsulated TGFβ alone (denoted as TPX6001) were significantly (P < 0.01) reduced from baseline levels. When tested in the SCID mouse CD4+CD25- adoptive cell transfer (ACT) model of IBD, oral TPX6001 alone provided only a transient benefit in terms of reduced weight loss. CONCLUSION: These observations suggest a negative feedback mechanism in the gut whereby local delivery of TGFβ results in reduced local and systemic levels of the active form of TGFβ. Our findings suggest potential clinical implications for use of encapsulated TGFβ, perhaps in the context of IBD and/or other instances of fibrosis and/or pathological TGFβ signaling. Baishideng Publishing Group Inc 2020-11-08 2020-11-08 /pmc/articles/PMC7667406/ /pubmed/33251033 http://dx.doi.org/10.4292/wjgpt.v11.i5.79 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/Licenses/by-nc/4.0/
spellingShingle Basic Study
Hammer, Laura
Furtado, Stacia
Mathiowitz, Edith
Auci, Dominick L
Oral encapsulated transforming growth factor β1 reduces endogenous levels: Effect on inflammatory bowel disease
title Oral encapsulated transforming growth factor β1 reduces endogenous levels: Effect on inflammatory bowel disease
title_full Oral encapsulated transforming growth factor β1 reduces endogenous levels: Effect on inflammatory bowel disease
title_fullStr Oral encapsulated transforming growth factor β1 reduces endogenous levels: Effect on inflammatory bowel disease
title_full_unstemmed Oral encapsulated transforming growth factor β1 reduces endogenous levels: Effect on inflammatory bowel disease
title_short Oral encapsulated transforming growth factor β1 reduces endogenous levels: Effect on inflammatory bowel disease
title_sort oral encapsulated transforming growth factor β1 reduces endogenous levels: effect on inflammatory bowel disease
topic Basic Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7667406/
https://www.ncbi.nlm.nih.gov/pubmed/33251033
http://dx.doi.org/10.4292/wjgpt.v11.i5.79
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