Publication: Therapeutic effect of adipose-derived mesenchymal stem cells (AD-MSCs) compared to pirfenidone on corticosteroid resistance in a mouse model of acute exacerbation of idiopathic pulmonary fibrosis
Authors
Fikry, Heba ; Saleh, Lobna A. ; Gawad, Sara Abdel
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Publisher
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DOI
https://doi.org/ 10.14670/HH-18-493
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info:eu-repo/semantics/article
Description
Abstract
Introduction. Acute exacerbation-idiopathic
pulmonary fibrosis (AE-IPF) is a life-threatening
condition. In the treatment of AE-IPF, corticosteroid
medication is commonly utilized. However, there is
insufficient evidence to justify its usage. Pirfenidone
(PFD) has recently been discovered to be effective in the
treatment of AE-IPF patients. However, regenerative
therapy, such as stem cell therapy or tissue engineering,
is necessary due to ineffective and limited therapies.
Combining MSC transplantation with pharmacological
therapy may also give additional benefits; nevertheless,
its use must be proven experimentally. As a result, the
goal of this study was to assess the therapeutic effects of
adipose-derived mesenchymal stem cells (AD-MSCs) on
corticosteroid resistance in an animal model of AE-IPF
caused by bleomycin compared to PFD.
Materials and methods. Seventy C57BL/6J male
mice were randomly divided into seven groups, control,
BLM, methylprednisolone (MP), PFD, AD-MSCs, PFD
+MP, and AD-MSCs +MP.
Results. In terms of survival, collagen deposition,
the acute lung injury score (ALI), and the Ashcroft
score, AD-MSCs exceeded PFD. AD-MSCs + MP
provided protection and preserved the lung's architecture
in BLM-induced AE. In addition, AD-MSCs
successfully decreased chemokine (CC motif) ligand-2
(CCL2) positive cells and lower pro-fibrotic and proinflammatory cytokines.
Conclusions. AD-MSCs enhanced histological
structure, Ashcroft and ALI scores, lung collagen
deposition, survival, and cytokines in an animal model
of AE-IPF. As a result, we believe that AD-MSCs may
be more therapeutically helpful for AE-IPF than
presently available therapies, either alone or in
conjunction with MP.
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Citation
Histology and Histopathology Vol. 37, nº11 (2022)
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