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Rosacea treatment with mussel adhesive protein delivered via microneedling: In vivo and clinical studies
Background Rosacea is a prevalent chronic dermatological condition marked by facial inflammation and erythema, significantly compromising the quality of life for affected individuals. Current treatment methods for rosacea are not considered ideal because of the complex etiology of the disease. Musse...
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Published in: | Journal of cosmetic dermatology 2024-05, Vol.23 (5), p.1654-1662 |
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creator | Luo, Yinli Nan, Meilan Dong, Richeng Jin, Qingmei Yuan, Jiachen Zhi, Jiahui Pi, Longquan Jin, Zhehu Jin, Chenglong |
description | Background
Rosacea is a prevalent chronic dermatological condition marked by facial inflammation and erythema, significantly compromising the quality of life for affected individuals. Current treatment methods for rosacea are not considered ideal because of the complex etiology of the disease. Mussel adhesive protein (MAP) is a glycoprotein derived from the foot gland of mussels. The protein exhibits anti‐inflammatory properties, relieves skin itching, and promotes wound healing.
Aims
We aimed to explore the feasibility of using MAP administered via microneedle delivery for treating rosacea and the potential molecular mechanism involved.
Materials and Methods
The therapeutic effect and mechanism of MAP microneedle delivery in an LL‐37‐induced rosacea‐like mouse model were observed using morphological and histological methods. Twenty‐seven patients with erythematotelangiectatic rosacea (ETR) underwent treatment once every 1 month, with three treatments constituting one treatment course. The therapeutic effect was evaluated by comparing the clinical images taken at baseline, after the first treatment course, and after the second treatment course. The red value, CEA, and GFSS score were also calculated.
Results
In response to the microneedle delivery of MAP, innate immunity, inflammatory infiltration, and abnormal neurovascular regulation improved significantly in rosacea‐like mice. In the clinical experiments, the microneedle delivery of MAP significantly improved the symptoms of erythema, flushing, and telangiectasia in patients with ETR, and no obvious adverse reactions were observed.
Conclusions
MAP delivered by microneedling is effective and safe for treating ETR. |
doi_str_mv | 10.1111/jocd.16190 |
format | article |
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Rosacea is a prevalent chronic dermatological condition marked by facial inflammation and erythema, significantly compromising the quality of life for affected individuals. Current treatment methods for rosacea are not considered ideal because of the complex etiology of the disease. Mussel adhesive protein (MAP) is a glycoprotein derived from the foot gland of mussels. The protein exhibits anti‐inflammatory properties, relieves skin itching, and promotes wound healing.
Aims
We aimed to explore the feasibility of using MAP administered via microneedle delivery for treating rosacea and the potential molecular mechanism involved.
Materials and Methods
The therapeutic effect and mechanism of MAP microneedle delivery in an LL‐37‐induced rosacea‐like mouse model were observed using morphological and histological methods. Twenty‐seven patients with erythematotelangiectatic rosacea (ETR) underwent treatment once every 1 month, with three treatments constituting one treatment course. The therapeutic effect was evaluated by comparing the clinical images taken at baseline, after the first treatment course, and after the second treatment course. The red value, CEA, and GFSS score were also calculated.
Results
In response to the microneedle delivery of MAP, innate immunity, inflammatory infiltration, and abnormal neurovascular regulation improved significantly in rosacea‐like mice. In the clinical experiments, the microneedle delivery of MAP significantly improved the symptoms of erythema, flushing, and telangiectasia in patients with ETR, and no obvious adverse reactions were observed.
Conclusions
MAP delivered by microneedling is effective and safe for treating ETR.</description><identifier>ISSN: 1473-2130</identifier><identifier>EISSN: 1473-2165</identifier><identifier>DOI: 10.1111/jocd.16190</identifier><identifier>PMID: 38284129</identifier><language>eng</language><publisher>England</publisher><subject>LL‐37 ; microneedle ; mussel adhesive protein ; rosacea</subject><ispartof>Journal of cosmetic dermatology, 2024-05, Vol.23 (5), p.1654-1662</ispartof><rights>2024 The Authors. published by Wiley Periodicals LLC.</rights><rights>2024 The Authors. Journal of Cosmetic Dermatology published by Wiley Periodicals LLC.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3240-9b3bb5b11326a1902d27a082d188ac4ea2508afd52c2a6be2a852b428acf72a23</cites><orcidid>0000-0002-1431-8744 ; 0000-0003-3753-1297 ; 0000-0002-2128-4618 ; 0000-0003-1049-1416</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjocd.16190$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjocd.16190$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,11562,27924,27925,37013,46052,46476</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38284129$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Luo, Yinli</creatorcontrib><creatorcontrib>Nan, Meilan</creatorcontrib><creatorcontrib>Dong, Richeng</creatorcontrib><creatorcontrib>Jin, Qingmei</creatorcontrib><creatorcontrib>Yuan, Jiachen</creatorcontrib><creatorcontrib>Zhi, Jiahui</creatorcontrib><creatorcontrib>Pi, Longquan</creatorcontrib><creatorcontrib>Jin, Zhehu</creatorcontrib><creatorcontrib>Jin, Chenglong</creatorcontrib><title>Rosacea treatment with mussel adhesive protein delivered via microneedling: In vivo and clinical studies</title><title>Journal of cosmetic dermatology</title><addtitle>J Cosmet Dermatol</addtitle><description>Background
Rosacea is a prevalent chronic dermatological condition marked by facial inflammation and erythema, significantly compromising the quality of life for affected individuals. Current treatment methods for rosacea are not considered ideal because of the complex etiology of the disease. Mussel adhesive protein (MAP) is a glycoprotein derived from the foot gland of mussels. The protein exhibits anti‐inflammatory properties, relieves skin itching, and promotes wound healing.
Aims
We aimed to explore the feasibility of using MAP administered via microneedle delivery for treating rosacea and the potential molecular mechanism involved.
Materials and Methods
The therapeutic effect and mechanism of MAP microneedle delivery in an LL‐37‐induced rosacea‐like mouse model were observed using morphological and histological methods. Twenty‐seven patients with erythematotelangiectatic rosacea (ETR) underwent treatment once every 1 month, with three treatments constituting one treatment course. The therapeutic effect was evaluated by comparing the clinical images taken at baseline, after the first treatment course, and after the second treatment course. The red value, CEA, and GFSS score were also calculated.
Results
In response to the microneedle delivery of MAP, innate immunity, inflammatory infiltration, and abnormal neurovascular regulation improved significantly in rosacea‐like mice. In the clinical experiments, the microneedle delivery of MAP significantly improved the symptoms of erythema, flushing, and telangiectasia in patients with ETR, and no obvious adverse reactions were observed.
Conclusions
MAP delivered by microneedling is effective and safe for treating ETR.</description><subject>LL‐37</subject><subject>microneedle</subject><subject>mussel adhesive protein</subject><subject>rosacea</subject><issn>1473-2130</issn><issn>1473-2165</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNp9kEtOwzAQhi0EoqWw4QDIS4TUYk-SJmGHyquoUiUE62hiT6irPEqctOptOAsnwyXQJd6M7fn0aeZn7FyKkXTnelkpPZJjGYsD1pd-6A1BjoPD_d0TPXZi7VIIGcYyOGY9L4LIlxD3mXmpLCpC3tSETUFlwzemWfCitZZyjnpB1qyJr-qqIVNyTbl71qT52iAvjKqrkkjnpny_4dPy63Nt1hXHUnPl_ozCnNum1YbsKTvKMLd09lsH7O3h_nXyNJzNH6eT29lQeeCLYZx6aRqkUnowRrcSaAhRRKBlFKHyCSEQEWY6AAU4TgkwCiD1wTWzEBC8AbvsvG7kj5ZskxTGKspzLKlqbQKxjEPfdxqHXnWo28LamrJkVZsC620iRbKLNtlFm_xE6-CLX2-bFqT36F-WDpAdsDE5bf9RJc_zyV0n_Qba14Xo</recordid><startdate>202405</startdate><enddate>202405</enddate><creator>Luo, Yinli</creator><creator>Nan, Meilan</creator><creator>Dong, Richeng</creator><creator>Jin, Qingmei</creator><creator>Yuan, Jiachen</creator><creator>Zhi, Jiahui</creator><creator>Pi, Longquan</creator><creator>Jin, Zhehu</creator><creator>Jin, Chenglong</creator><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1431-8744</orcidid><orcidid>https://orcid.org/0000-0003-3753-1297</orcidid><orcidid>https://orcid.org/0000-0002-2128-4618</orcidid><orcidid>https://orcid.org/0000-0003-1049-1416</orcidid></search><sort><creationdate>202405</creationdate><title>Rosacea treatment with mussel adhesive protein delivered via microneedling: In vivo and clinical studies</title><author>Luo, Yinli ; Nan, Meilan ; Dong, Richeng ; Jin, Qingmei ; Yuan, Jiachen ; Zhi, Jiahui ; Pi, Longquan ; Jin, Zhehu ; Jin, Chenglong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3240-9b3bb5b11326a1902d27a082d188ac4ea2508afd52c2a6be2a852b428acf72a23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>LL‐37</topic><topic>microneedle</topic><topic>mussel adhesive protein</topic><topic>rosacea</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Luo, Yinli</creatorcontrib><creatorcontrib>Nan, Meilan</creatorcontrib><creatorcontrib>Dong, Richeng</creatorcontrib><creatorcontrib>Jin, Qingmei</creatorcontrib><creatorcontrib>Yuan, Jiachen</creatorcontrib><creatorcontrib>Zhi, Jiahui</creatorcontrib><creatorcontrib>Pi, Longquan</creatorcontrib><creatorcontrib>Jin, Zhehu</creatorcontrib><creatorcontrib>Jin, Chenglong</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Free Archive</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cosmetic dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Luo, Yinli</au><au>Nan, Meilan</au><au>Dong, Richeng</au><au>Jin, Qingmei</au><au>Yuan, Jiachen</au><au>Zhi, Jiahui</au><au>Pi, Longquan</au><au>Jin, Zhehu</au><au>Jin, Chenglong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rosacea treatment with mussel adhesive protein delivered via microneedling: In vivo and clinical studies</atitle><jtitle>Journal of cosmetic dermatology</jtitle><addtitle>J Cosmet Dermatol</addtitle><date>2024-05</date><risdate>2024</risdate><volume>23</volume><issue>5</issue><spage>1654</spage><epage>1662</epage><pages>1654-1662</pages><issn>1473-2130</issn><eissn>1473-2165</eissn><abstract>Background
Rosacea is a prevalent chronic dermatological condition marked by facial inflammation and erythema, significantly compromising the quality of life for affected individuals. Current treatment methods for rosacea are not considered ideal because of the complex etiology of the disease. Mussel adhesive protein (MAP) is a glycoprotein derived from the foot gland of mussels. The protein exhibits anti‐inflammatory properties, relieves skin itching, and promotes wound healing.
Aims
We aimed to explore the feasibility of using MAP administered via microneedle delivery for treating rosacea and the potential molecular mechanism involved.
Materials and Methods
The therapeutic effect and mechanism of MAP microneedle delivery in an LL‐37‐induced rosacea‐like mouse model were observed using morphological and histological methods. Twenty‐seven patients with erythematotelangiectatic rosacea (ETR) underwent treatment once every 1 month, with three treatments constituting one treatment course. The therapeutic effect was evaluated by comparing the clinical images taken at baseline, after the first treatment course, and after the second treatment course. The red value, CEA, and GFSS score were also calculated.
Results
In response to the microneedle delivery of MAP, innate immunity, inflammatory infiltration, and abnormal neurovascular regulation improved significantly in rosacea‐like mice. In the clinical experiments, the microneedle delivery of MAP significantly improved the symptoms of erythema, flushing, and telangiectasia in patients with ETR, and no obvious adverse reactions were observed.
Conclusions
MAP delivered by microneedling is effective and safe for treating ETR.</abstract><cop>England</cop><pmid>38284129</pmid><doi>10.1111/jocd.16190</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-1431-8744</orcidid><orcidid>https://orcid.org/0000-0003-3753-1297</orcidid><orcidid>https://orcid.org/0000-0002-2128-4618</orcidid><orcidid>https://orcid.org/0000-0003-1049-1416</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | LL‐37 microneedle mussel adhesive protein rosacea |
title | Rosacea treatment with mussel adhesive protein delivered via microneedling: In vivo and clinical studies |
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