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      In vitro and in vivo efficacy of the Active Oligo Skin complex™, a new active ingredient processed from seawater, on multiple parameters of atopic skin

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          Abstract

          Background

          Different symptoms are associated with atopic skin, including dryness, pruritus and pain, and affect patients’ quality of life. The environment, microbiota, epidermis, immune and nerve cells are all implicated in the pathogenesis of atopic skin. Staphylococcus aureus is the focus of particular attention. Epidermis is implicated at multiple levels: inflammatory process, barrier, control of moisture and water loss. Sensory neurons that participate in cutaneous neurogenic inflammation and pruritus are seen as a potential new target. Specific management strategies and new treatments for adults and children are needed to help in more refractory cases. As a baseline of management, guidelines recommend a treatment to moisturize the skin and maintain the skin barrier function, such as an emollient.

          Objectives

          To evaluate a new product in vitro and in vivo in order to validate the potential of its use in people with atopic skin or dry skin.

          Methods

          A specific mineral composition, Active Oligo Skin complex™, from seawater was developed and included in a balm. The effects of a solution and balm containing the complex were evaluated in vitro on the growth and biofilm formation of Staphylococcus aureus and Staphylococcus epidermidis in different skin models, and in vivo in adult and young volunteers.

          Results

          In vitro, the complex modulated bacterial biofilm formation and growth, decreased cytokine [interleukin (IL)-1, IL-6, IL-4] and neuropeptide (substance P) release, and increased the expression of CL1 and CL4. On volunteers with dry skin, the complex had a moisturizing effect after 1 h of application. Dryness and roughness were also reduced in young participants with atopic skin. The balm decreased erythema and pruritus after 21 days of topical application on 60 young participants. On 22 adult participants, stinging score was decreased after ­application.

          Conclusions

          The Active Oligo Skin complex™ appears to display potent antipruritic and anti-inflammatory activities, both in vitro and in vivo.

          Abstract

          In our paper, the Active Oligo Skin complex™, processed from sea water and possessing specific mineral composition, was developed and included in a balm. The effects of solution and balm containing the complex were evaluated in vitro on bacteria growth and biofilm formation of S. aureus and S. epidermidis, on different skin models, and in vivo on adult and young volunteers. In summary, the Active Oligo Skin complex™ appears to display in vitro and in vivo potent antipruritic and anti-inflammatory activities.

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          Most cited references49

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          The human skin microbiome

          Functioning as the exterior interface of the human body with the environment, skin acts as a physical barrier to prevent the invasion of foreign pathogens while providing a home to the commensal microbiota. The harsh physical landscape of skin, particularly the desiccated, nutrient-poor, acidic environment, also contributes to the adversity that pathogens face when colonizing human skin. Despite this, the skin is colonized by a diverse microbiota. In this Review, we describe amplicon and shotgun metagenomic DNA sequencing studies that have been used to assess the taxonomic diversity of microorganisms that are associated with skin from the kingdom to the strain level. We discuss recent insights into skin microbial communities, including their composition in health and disease, the dynamics between species and interactions with the immune system, with a focus on Propionibacterium acnes, Staphylococcus epidermidis and Staphylococcus aureus.
            • Record: found
            • Abstract: found
            • Article: found
            Is Open Access

            Diversity of the Human Skin Microbiome Early in Life

            Within days after birth, rapid surface colonization of infant skin coincides with significant functional changes. Gradual maturation of skin function, structure, and composition continues throughout the first years of life. Recent reports have revealed topographical and temporal variations in the adult skin microbiome. Here we address the question of how the human skin microbiome develops early in life. We show that the composition of cutaneous microbial communities evolves over the first year of life, showing increasing diversity with age. Although early colonization is dominated by Staphylococci, their significant decline contributes to increased population evenness by the end of the first year. Similar to what has been shown in adults, the composition of infant skin microflora appears to be site specific. In contrast to adults, we find that Firmicutes predominate on infant skin. Timely and proper establishment of healthy skin microbiome during this early period might have a pivotal role in denying access to potentially infectious microbes and could affect microbiome composition and stability extending into adulthood. Bacterial communities contribute to the establishment of cutaneous homeostasis and modulate inflammatory responses. Early microbial colonization is therefore expected to critically affect the development of the skin immune function.
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              • Article: not found

              Functions of the skin microbiota in health and disease.

              The skin, the human body's largest organ, is home to a diverse and complex variety of innate and adaptive immune functions. Despite this potent immune system present at the cutaneous barrier, the skin encourages colonization by microorganisms. Characterization these microbial communities has enhanced our knowledge of the ecology of organisms present in normal skin; furthermore, studies have begun to bring to light the intimate relationships shared between host and resident microbes. In particular, it is apparent that just as host immunological factors and behaviors shape the composition of these communities, microbes present on the skin greatly impact the functions of human immunity. Thus, today the skin immune system should be considered a collective mixture of elements from the host and microbes acting in a mutualistic relationship. In this article we will review recent findings of the interactions of skin microbial communities with host immunity, and discuss the role that dysbiosis of these communities plays in diseases of the skin.

                Author and article information

                Contributors
                Journal
                Skin Health Dis
                Skin Health Dis
                skinhd
                Skin Health and Disease
                Oxford University Press (UK )
                2690-442X
                February 2025
                14 February 2025
                14 February 2025
                : 5
                : 1
                : 22-30
                Affiliations
                University of Brest, LIEN , Brest, France
                Unité de Recherche 4312 Communication Bactérienne et Stratégies Anti-infectieuses (UR CBSA), Université de Rouen Normandie , Evreux, France
                Unité de Recherche 4312 Communication Bactérienne et Stratégies Anti-infectieuses (UR CBSA), Université de Rouen Normandie , Evreux, France
                Centre d'Expertise Cosmetomics@URN, Université de Rouen Normandie , Evreux, France
                University of Brest, LIEN , Brest, France
                University of Brest, LIEN , Brest, France
                University of Brest, LIEN , Brest, France
                University of Brest, LIEN , Brest, France
                University of Brest, LIEN , Brest, France
                Laboratoires Gilbert , R&D Department, Hérouville St Clair, France
                Laboratoires Gilbert , R&D Department, Hérouville St Clair, France
                Laboratoires Gilbert , R&D Department, Hérouville St Clair, France
                Author notes
                Correspondence: Nicolas Lebonvallet. Email: nicolas.lebonvallet@ 123456univ-brest.fr

                Conflict of interest: N.L., C.C., M.G.F. and L.M. have a conflict of interest with Laboratoires Gilbert. E.S., S.C. and J.G. are employees of Laboratoires Gilbert.

                Article
                vzae029
                10.1093/skinhd/vzae029
                11924379
                90806f85-4f01-4857-86d0-cbb171c2e7b0
                © The Author(s) 2025. Published by Oxford University Press on behalf of British Association of Dermatologists.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                Page count
                Pages: 9
                Categories
                Original Article
                AcademicSubjects/MED00010
                AcademicSubjects/MED00160
                AcademicSubjects/MED00240

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