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<journal-id journal-id-type="publisher-id">Front. Bioeng. Biotechnol.</journal-id>
<journal-title>Frontiers in Bioengineering and Biotechnology</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Bioeng. Biotechnol.</abbrev-journal-title>
<issn pub-type="epub">2296-4185</issn>
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<publisher-name>Frontiers Media S.A.</publisher-name>
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<article-id pub-id-type="publisher-id">1642526</article-id>
<article-id pub-id-type="doi">10.3389/fbioe.2025.1642526</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Bioengineering and Biotechnology</subject>
<subj-group>
<subject>Correction</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>Correction: An engineered adipose formulation decreases hepatic inflammation and fibrosis in a rodent model of metabolic dysfunction-associated steatotic liver disease</article-title>
<alt-title alt-title-type="left-running-head">Choi et al.</alt-title>
<alt-title alt-title-type="right-running-head">
<ext-link ext-link-type="uri" xlink:href="https://doi.org/10.3389/fbioe.2025.1642526">10.3389/fbioe.2025.1642526</ext-link>
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<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Choi</surname>
<given-names>Youngshim</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
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<contrib contrib-type="author">
<name>
<surname>Ma</surname>
<given-names>Yinyan</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
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<contrib contrib-type="author">
<name>
<surname>Tom</surname>
<given-names>Samson</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
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<contrib contrib-type="author" corresp="yes" equal-contrib="yes">
<name>
<surname>Danilkovitch</surname>
<given-names>Alla</given-names>
</name>
<xref ref-type="aff" rid="aff2">
<sup>2</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>&#x2020;</sup>
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<contrib contrib-type="author" corresp="yes" equal-contrib="yes">
<name>
<surname>Yu</surname>
<given-names>Liqing</given-names>
</name>
<xref ref-type="aff" rid="aff1">
<sup>1</sup>
</xref>
<xref ref-type="corresp" rid="c001">&#x2a;</xref>
<xref ref-type="author-notes" rid="fn001">
<sup>&#x2020;</sup>
</xref>
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<aff id="aff1">
<sup>1</sup>
<institution>Division of Endocrinology</institution>, <institution>Diabetes and Nutrition, Department of Medicine</institution>, <institution>University of Maryland School of Medicine</institution>, <addr-line>Baltimore</addr-line>, <addr-line>MD</addr-line>, <country>United States</country>
</aff>
<aff id="aff2">
<sup>2</sup>
<institution>Britecyte, Inc.</institution>, <addr-line>Fredrick</addr-line>, <addr-line>MD</addr-line>, <country>United States</country>
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<author-notes>
<fn fn-type="edited-by">
<p>
<bold>Edited and reviewed by:</bold> <ext-link ext-link-type="uri" xlink:href="https://loop.frontiersin.org/people/601394/overview">Luca Urbani</ext-link>, Foundation for Liver Research, United Kingdom</p>
</fn>
<corresp id="c001">&#x2a;Correspondence: Alla Danilkovitch, <email>adanilkovitch@britecyte.com</email>; Liqing Yu, <email>lyu@som.umaryland.edu</email>
</corresp>
<fn fn-type="equal" id="fn001">
<label>
<sup>&#x2020;</sup>
</label>
<p>These authors have contributed equally to this work</p>
</fn>
</author-notes>
<pub-date pub-type="epub">
<day>26</day>
<month>06</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="collection">
<year>2025</year>
</pub-date>
<volume>13</volume>
<elocation-id>1642526</elocation-id>
<history>
<date date-type="received">
<day>06</day>
<month>06</month>
<year>2025</year>
</date>
<date date-type="accepted">
<day>18</day>
<month>06</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#xa9; 2025 Choi, Ma, Tom, Danilkovitch and Yu.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Choi, Ma, Tom, Danilkovitch and Yu</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<related-article id="RA1" related-article-type="corrected-article" journal-id="Front. Bioeng. Biotechnol." journal-id-type="nlm-ta" xlink:href="10.3389/fbioe.2025.1579062" ext-link-type="doi">A Correction on <article-title>An engineered adipose formulation decreases hepatic inflammation and fibrosis in a rodent model of metabolic dysfunction-associated steatotic liver disease</article-title> by Choi Y, Ma Y, Tom S, Danilkovitch A and Yu L (2025). Front. Bioeng. Biotechnol. 13:1579062. doi: <object-id>10.3389/fbioe.2025.1579062</object-id>
</related-article>
<kwd-group>
<kwd>adipose tissue</kwd>
<kwd>adipose stem cells</kwd>
<kwd>tissue engineering</kwd>
<kwd>MASLD</kwd>
<kwd>fibrosis</kwd>
<kwd>inflammation</kwd>
</kwd-group>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Cell and Gene Therapy</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<p>In the published article, there was an error in <xref ref-type="fig" rid="F7">Figure 7B</xref> as published. The graph in <xref ref-type="fig" rid="F7">Figure 7B</xref> was identical to <xref ref-type="fig" rid="F7">Figure 7A</xref>, and has been replaced with the correct version. The corrected <xref ref-type="fig" rid="F7">Figure 7B</xref> and its caption &#x201c;FIGURE 7: In vivo immunogenicity of xenogeneic hAF and allogeneic rAF in rats. Detection of (A) anti-hAF or (B) anti-rAF antibodies by ELISA coated with hAF or rAF extracts, respectively. Control: serum from rats treated with PBS. Background: no serum. Data are presented as mean &#xb1; SD by OD at 450 nm for each serum concentration (n &#x3d; 6/group).&#x201d; appear below.</p>
<fig id="F7" position="float">
<label>FIGURE 7</label>
<caption>
<p>
<italic>In vivo</italic> immunogenicity of xenogeneic hAF and allogeneic rAF in rats. Detection of <bold>(A)</bold> anti-hAF or <bold>(B)</bold> anti-rAF antibodies by ELISA coated with hAF or rAF extracts, respectively. Control: serum from rats treated with PBS. Background: no serum. Data are presented as mean &#xb1; SD by OD at 450&#xa0;nm for each serum concentration (n &#x3d; 6/group).</p>
</caption>
<graphic xlink:href="fbioe-13-1642526-g007.tif">
<alt-text content-type="machine-generated">Two graphs showing antibody detection in rats. Panel A: Human formulation (xenogen) shows decreasing anti-hAF antibodies with lower serum titration. Panel B: Rat formulation (allogen) shows stable anti-rAF antibodies across titrations. Both graphs include lines for PBS, hAF/rAF, and background, with OD450 on the y-axis and serum titration (%) on the x-axis.</alt-text>
</graphic>
</fig>
<p>The original version of this article has been updated.</p>
</body>
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<title>Publisher&#x2019;s note</title>
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