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<ArticleSet>
<Article>
<Journal>
				<PublisherName>AmitisGen TECH Dev Group</PublisherName>
				<JournalTitle>Personalized and Precision Medicine Journal</JournalTitle>
				<Issn>3115-7874</Issn>
				<Volume>8</Volume>
				<Issue>30</Issue>
				<PubDate PubStatus="epublish">
					<Year>2023</Year>
					<Month>09</Month>
					<Day>28</Day>
				</PubDate>
			</Journal>
<ArticleTitle>Adjustment of a Fibrosis Marker, Pro-Inflammatory Cytokines, and IgE in Asthmatic Animals</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>32</FirstPage>
			<LastPage>40</LastPage>
			<ELocationID EIdType="pii">707859</ELocationID>
			
<ELocationID EIdType="doi">10.22034/pmj.2023.2009908.1010</ELocationID>
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Fereshteh</FirstName>
					<LastName>Dalouchi</LastName>
<Affiliation>Physiology Research Center, Iran University of Medical Sciences, Tehran, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Zeynab</FirstName>
					<LastName>Sharifi Aghdam</LastName>
<Affiliation>Physiology Research Center, Iran University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Raza</FirstName>
					<LastName>Falak</LastName>
<Affiliation>Department of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Morteza</FirstName>
					<LastName>Bakhshesh</LastName>
<Affiliation>Khomein University of Medical Sciences, Khomein, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Maryam</FirstName>
					<LastName>Hajidazeh</LastName>
<Affiliation>Department of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Maryam</FirstName>
					<LastName>Naseroleslami</LastName>
<Affiliation>Department of Cellular and Molecular Biology, Faculty of Advanced Science and Technology, &amp;lrm;Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Mahdieh</FirstName>
					<LastName>Mehrab Mohseni</LastName>
<Affiliation>Department of Cellular and Molecular Biology, Faculty of Advanced Science and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran</Affiliation>

</Author>
<Author>
					<FirstName>Yaser</FirstName>
					<LastName>Azizi</LastName>
<Affiliation>Physiology Research Center, Iran University of Medical Sciences, Tehran, Iran.</Affiliation>

</Author>
<Author>
					<FirstName>Nahid</FirstName>
					<LastName>Aboutaleb</LastName>
<Affiliation>Physiology Research Center, Iran University of Medical Sciences, Tehran, Iran.</Affiliation>
<Identifier Source="ORCID">0000-0002-7514-5939</Identifier>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2023</Year>
					<Month>05</Month>
					<Day>07</Day>
				</PubDate>
			</History>
		<Abstract>&lt;strong&gt;Background&lt;/strong&gt;: A lot of patients are suffering from asthma. For decreasing the asthma symptoms, we studied the effects of conditioned medium (CM) of human amniotic membrane mesenchymal stem cells (hAM-MSCs) as a source of anti-inflammatory cytokines on splenocyte and lung tissue of asthmatic Balb/c mice.&lt;br&gt;&lt;strong&gt;Methods:&lt;/strong&gt; Forty mice were categorized into four groups; ovalbumin (OVA)-induced asthma, CM-treated asthma, DMEM (Dulbecco&#039;s Modified Eagle Medium)-treated asthma, and saline control. Each group received related treatment. The lung alpha-smooth muscle actin (α-SMA)  and splenocyte inflammatory cytokines and IgE were examined through Western blot analysis.&lt;br&gt;&lt;strong&gt;Results:&lt;/strong&gt; Western blot showed α-SMA overexpression in the OVA and DMEM groups compared with the saline group. CM therapy could significantly reverse it compared with OVA and OVA+DMEM categories by elevating IL-10 and IFN-γ and reducing IL-4, IgE, and TGF-β .&lt;br&gt;&lt;strong&gt;Conclusion:&lt;/strong&gt; CM treatment could improve asthma symptoms by adjusting α-SMA in lung tissue and pro-inflammatory cytokines and IgE in splenocytes.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Asthma</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Alpha-smooth muscle actin</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">Mesenchymal stem cell</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://www.pmjournal.ir/article_707859_dd482b494ff0641c71e1e709449f29e7.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
