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The inflammatory lung microenvironment; a key mediator in msc licensing

Dunbar, Hazel ; Weiss, Daniel J. ; Enes, Sara Rolandsson LU orcid ; Laffey, John G. and English, Karen (2021) In Cells 10(11).
Abstract

Recent clinical trials of mesenchymal stromal cell (MSC) therapy for various inflammatory conditions have highlighted the significant benefit to patients who respond to MSC administration. Thus, there is strong interest in investigating MSC therapy in acute inflammatory lung conditions, such as acute respiratory distress syndrome (ARDS). Unfortunately, not all patients respond, and evidence now suggests that the differential disease microenvironment present across patients and sub-phenotypes of disease or across disease severities influences MSC licensing, function and therapeutic efficacy. Here, we discuss the importance of licensing MSCs and the need to better under-stand how the disease microenvironment influences MSC activation and... (More)

Recent clinical trials of mesenchymal stromal cell (MSC) therapy for various inflammatory conditions have highlighted the significant benefit to patients who respond to MSC administration. Thus, there is strong interest in investigating MSC therapy in acute inflammatory lung conditions, such as acute respiratory distress syndrome (ARDS). Unfortunately, not all patients respond, and evidence now suggests that the differential disease microenvironment present across patients and sub-phenotypes of disease or across disease severities influences MSC licensing, function and therapeutic efficacy. Here, we discuss the importance of licensing MSCs and the need to better under-stand how the disease microenvironment influences MSC activation and therapeutic actions, in addition to the need for a patient-stratification approach.

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Please use this url to cite or link to this publication:
author
; ; ; and
organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
Cytokines, Immunomodulatory, Inflammatory, Licensing, Lung, Microenvironment, MSC
in
Cells
volume
10
issue
11
article number
2982
publisher
MDPI AG
external identifiers
  • scopus:85118272707
  • pmid:34831203
ISSN
2073-4409
DOI
10.3390/cells10112982
language
English
LU publication?
yes
additional info
Publisher Copyright: © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
id
9236a25d-f104-40b5-9136-b15a5d802275
date added to LUP
2021-11-22 13:07:51
date last changed
2024-06-15 21:10:40
@article{9236a25d-f104-40b5-9136-b15a5d802275,
  abstract     = {{<p>Recent clinical trials of mesenchymal stromal cell (MSC) therapy for various inflammatory conditions have highlighted the significant benefit to patients who respond to MSC administration. Thus, there is strong interest in investigating MSC therapy in acute inflammatory lung conditions, such as acute respiratory distress syndrome (ARDS). Unfortunately, not all patients respond, and evidence now suggests that the differential disease microenvironment present across patients and sub-phenotypes of disease or across disease severities influences MSC licensing, function and therapeutic efficacy. Here, we discuss the importance of licensing MSCs and the need to better under-stand how the disease microenvironment influences MSC activation and therapeutic actions, in addition to the need for a patient-stratification approach.</p>}},
  author       = {{Dunbar, Hazel and Weiss, Daniel J. and Enes, Sara Rolandsson and Laffey, John G. and English, Karen}},
  issn         = {{2073-4409}},
  keywords     = {{Cytokines; Immunomodulatory; Inflammatory; Licensing; Lung; Microenvironment; MSC}},
  language     = {{eng}},
  number       = {{11}},
  publisher    = {{MDPI AG}},
  series       = {{Cells}},
  title        = {{The inflammatory lung microenvironment; a key mediator in msc licensing}},
  url          = {{http://dx.doi.org/10.3390/cells10112982}},
  doi          = {{10.3390/cells10112982}},
  volume       = {{10}},
  year         = {{2021}},
}