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Mesenchymal stromal cell exosome -treated monocytes and uses thereof

A mononuclear cell and exosome technology, applied in animal cells, vertebrate cells, bone/connective tissue cells, etc., can solve the problems of lack of treatment, fatal IPF, and survival rate less than 10%

Pending Publication Date: 2021-03-09
CHILDRENS MEDICAL CENT CORP
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Lack of complete understanding of the underlying mechanisms of the disease can lead to lack of successful treatment
Despite two newly approved drugs, IPF remains deadly, with less than 10% five-year survival rate

Method used

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  • Mesenchymal stromal cell exosome -treated monocytes and uses thereof
  • Mesenchymal stromal cell exosome -treated monocytes and uses thereof
  • Mesenchymal stromal cell exosome -treated monocytes and uses thereof

Examples

Experimental program
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Embodiment

[0082] Idiopathic pulmonary fibrosis (IPF) is a chronic progressive respiratory disease whose underlying mechanisms are not fully understood and currently lack effective treatments. Although treatment with mesenchymal stromal cells (MSCs) has provided promising results in the prevention of pulmonary fibrosis, limitations of cell therapy continue to make cell-free therapies highly desirable. In preclinical models other than IPF, MSC extracellular vesicles (EVs) or more specifically exosomes (MEx) isolated from the MSC secretome have been shown to serve as therapeutic vehicles. The role of MEx and its mechanism of action (MOA) in IPF are unclear.

[0083] Objective: To study the potency and MOA of MEx in the bleomycin-IPF model.

[0084]METHODS: Exosomes (MEx) isolated from human bone marrow MCS were injected into adult C57BL / 6 mice 0 or 7 days after intratracheal bleomycin instillation. Lung and bone marrow-derived mononuclear cells (BMDMo) were collected on days 7 and 14 for...

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Abstract

Provided herein are methods of modulating monocyte phenotypes using isolated mesenchymal stem cell (MSC) exosomes. Monocytes treated with MSC exosomes can be used to treat fibrotic disease and autoimmune diseases.

Description

[0001] related application [0002] This application claims the benefit under 35 U.S.C. §119(e) of U.S. Provisional Application No. 62 / 669,324, filed May 9, 2018, entitled "MESENCHYMALSTROMAL CELL EXOSOME-TREATED MONOCYTES AND USES THEREOF," the entire contents of which are incorporated by reference Incorporated into this article. Background technique [0003] Idiopathic pulmonary fibrosis (IPF) is a chronic progressive respiratory disease with a prevalence of 0.5 to 27.9 per 100,000 person-years. Lack of a complete understanding of the mechanisms underlying this disease can lead to a lack of successful treatment. Despite two newly approved drugs, IPF remains fatal, with a five-year survival rate of less than 10%. Contents of the invention [0004] Here we show that a single intravenous (IV) dose of mesenchymal stem cell (MSC) exosomes reverses bleomycin-induced lung fibrosis at least in part by modulating the monocyte phenotype and reducing Alveolar epithelial cells (AEC...

Claims

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Application Information

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IPC IPC(8): A61K35/15C12N5/0786
CPCA61K35/28A61K35/51C12N5/0645C12N2502/1358A61P11/00A61P29/00A61K31/496A61K31/4418A61K39/4622A61K2239/31A61K39/4614A61K2239/38A61K39/464A61P37/02A61K35/15A61K45/06
Inventor 斯特兰·库雷姆巴纳斯S·亚历山大·米特西利斯
Owner CHILDRENS MEDICAL CENT CORP
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