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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
Main Authors: Luo, Yinli, Nan, Meilan, Dong, Richeng, Jin, Qingmei, Yuan, Jiachen, Zhi, Jiahui, Pi, Longquan, Jin, Zhehu, Jin, Chenglong
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container_end_page 1662
container_issue 5
container_start_page 1654
container_title Journal of cosmetic dermatology
container_volume 23
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
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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. 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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. 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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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