Compositions Comprising Bacterial Strain Lactobacillus paracasei and Hyaluronic Acid and Their Use for the Treatment of Skin

Abstract

The present invention relates to a composition comprising a probiotic (a live, viable or inactivated bacterial strain) and hyaluronic acid or a salt thereof for use in the prevention, treatment (therapeutic or cosmetic treatment) or attenuation of at least one sign or symptom associated with or caused by skin aging, a weakening of the skin's immune defenses, or skin inflammation / infection, such as inflammation induced or caused by ultraviolet light.

Description

[Technical field]

[0001] The present invention relates to a composition comprising a probiotic (a live or inactivated bacterial strain) and hyaluronic acid or a salt thereof for use in the prevention, treatment (therapeutic or cosmetic remedy) or attenuation of at least one sign or symptom associated with or caused by skin aging, a weakening of the skin's immune defenses, or skin inflammation / infection, such as inflammation induced or caused by ultraviolet radiation. [Background technology]

[0002] The skin is the outermost lining of the human body and constitutes the body's first line of defense against external attacks, given that it acts as an anatomical barrier against potential pathogens and harmful substances. Skin changes can promote the development of skin diseases, especially those caused by pathogens. For example, as the skin ages, it becomes thinner and more fragile, this is because cell renewal slows down, from the usual 3-4 weeks to 4-6 weeks. Over time, the skin undergoes structural changes, caused by several factors of different origins, that determine the loss of skin hydration, the development of microwrinkles, loss of elasticity, hyperkeratosis, and the formation of hyperpigmented spots.

[0003] Moreover, the abundant microbiota colonizing human skin plays important and useful functions in combating the attachment and development of skin pathogens such as Staphylococcus aureus, Pseudomonas aeruginosa, and Propionibacterium acnes, and may face imbalances or dysbiosis due to various factors.

[0004] When dysbiosis occurs on the skin, probiotics can act as modulators and restore balance at the level of the skin microbiota. In the last decade, the use of new technologies has facilitated the taxonomic analysis of the skin microbiota, whose bacterial population is approximately 1010 species of microorganisms belonging to more than 25 phyla, among which the most representative are Actinobacteria, Firmicutes, and Proteobacteria. Various skin diseases are associated with alterations in the skin microbiota, for example, Propionibacterium acnes is considered a pathogen associated with skin acne. Therefore, maintaining the homeostatic situation of the skin microbiota or restoring said homeostasis after microbial dysbiosis is fundamental for preventing or treating skin diseases, in particular skin infections or inflammations, and even more specifically infections or inflammations caused by pathogens such as bacteria or viruses, as well as infections or inflammations caused by exposure of the skin to ultraviolet radiation or unfavorable conditions.

[0005] Classically, these problems are approached with the use of antimicrobial agents, i.e., antiseptics and topical antibiotics. On the one hand, antibiotics are undoubtedly effective, but in addition to eliminating beneficial bacteria, prolonged use, especially of broad-spectrum antibiotics, poses the risk of sensitization and potential adverse events.

[0006] Moreover, the conventional approach to prevent UV radiation damage and skin aging problems is to use creams or skin-related products that reflect or absorb UV rays, commonly called sunscreens. The active ingredients of the so-called "chemical" solar filters (salicylates, cinnamates, oxybenzone, octylcrylene, etc.) are able to absorb UV rays thanks to their structure. On the other hand, titanium dioxide and zinc oxide are inert mineral substances that have a strong covering power and physically reflect the sunlight, and therefore are included in the so-called physical screens. Summary of the Invention [Problem to be solved by the invention]

[0007] However, said solar filters can only prevent the interaction of UV rays with the skin, do not stimulate the maintenance of homeostasis of the skin microflora, and cannot restore said homeostasis in case of dysbiosis or infections or inflammations caused by said UV rays that may not be completely shielded by the solar filters. [Means for solving the problem]

[0008] Following intensive research and development activities, the Applicant has addressed and solved the aforementioned technical problem by providing an innovative composition (in short, the composition of the present invention) comprising a mixture (in short, the mixture of the present invention) comprising or consisting of a live and viable or inactivated bacterial strain belonging to the species Lactobacillus paracasei identified as Lactobacillus paracasei LPC-S01DSM26760 and hyaluronic acid or a salt thereof (for short, HA).

[0009] Summary of the invention A first aspect of the present invention relates to the use of a composition comprising probiotics and hyaluronic acid or a salt thereof to prevent, reduce or treat skin ageing, e.g. natural skin ageing or skin ageing caused by exposure to external factors such as UV radiation.

[0010] A second aspect of the invention relates to the use of a composition comprising a probiotic and hyaluronic acid or a salt thereof to prevent, alleviate or treat at least one sign or symptom associated with or caused by a weakened immune defense of the skin.

[0011] A third aspect of the present invention relates to the use of a composition comprising probiotics and hyaluronic acid or a salt thereof for preventing, alleviating or treating at least one sign or symptom associated with or caused by skin inflammation / infection.

[0012] Particularly useful probiotics for the purposes of the present invention are bacteria belonging to the genus Lactobacillus, preferably belonging to the species Lactobacillus paracasei, for example L. paracasei strain LPC-S01 DSM 26760.

[0013] The applicant has indeed discovered that a composition comprising a probiotic, preferably a bacterium belonging to the genus Lactobacillus, and hyaluronic acid, is able to enhance the immune defense by promoting the release of antimicrobial peptides and chemokines in the skin, enhance the normal processes of epidermal differentiation and cell replacement, and strengthen the structure of the dermis.

[0014] Furthermore, the applicant has discovered that the use of a composition comprising hyaluronic acid and a probiotic, preferably a bacterium belonging to the genus Lactobacillus, can perform an anti-inflammatory effect and prevent the activation of inflammation induced or caused by ultraviolet light.

[0015] In particular, the compositions and mixtures of the present invention comprise: - triggering skin defense and / or healing mechanisms, in particular immunomodulatory mechanisms; - Prevent and / or treat inflammatory or infectious skin diseases, especially those induced by UV radiation, both UV-A and UV-B; - Combats the growth of pathogenic bacteria on the skin; - Maintaining or restoring the homeostatic state of the skin and / or the balance of the skin microbiota; - favoring, facilitating, promoting and / or accelerating the wound healing process and / or the re-epithelialization and / or scarring process; - Combating and / or slowing down skin aging; It is possible to do the following.

[0016] Furthermore, the compositions of the present invention can induce and / or promote positive effects, both short-term and long-term.

[0017] Furthermore, the mixtures and compositions of the present invention have no significant adverse effects and they can be administered to all subjects, particularly pediatric subjects and pregnant or lactating women.

[0018] Finally, the mixtures and / or compositions of the present invention are easy and cost effective to prepare.

[0019] These and other objects that will become apparent from the following detailed description are achieved by the mixtures and compositions (including said mixtures) of the present invention thanks to the technical features set out in the appended claims.

[0020] The present invention is explained in detail below and illustrated with reference to the accompanying drawings, in which: [Brief description of the drawings]

[0021] [Figure 1] FIG. 1 shows 20× and 40× magnification images of histological tissue sections, marked with Masson's trichrome staining, treated respectively with saline (A) and with a composition containing the strain LPC-S01 (B). [Diagram 2] FIG. 2 shows 20× and 40× magnification images of histological tissue sections treated with a composition containing hyaluronic acid (A) and a composition containing LPC-S01+hyaluronic acid strain (B), respectively, marked with Masson's trichrome stain. [Diagram 3] FIG. 3 shows quantification of nuclear translocation of NFκB in tissues exposed to UV light and treated with a composition comprising LPC-S01 strain (P1), a composition comprising LPC-S01 strain + hyaluronic acid (P2), and a composition comprising hyaluronic acid (P3). [Figure 4] FIG. 4 shows 20x magnification images of histological tissue sections treated with saline (A), a composition containing the LPC-S01 strain (B), a composition containing hyaluronic acid (C), and a composition containing the LPC-S01 strain and hyaluronic acid (D), marked with hematoxylin-eosin staining, 4 hours after UV injury. [Diagram 5]FIG. 5 shows 20x magnification images of histological tissue sections treated with saline (A), a composition containing the LPC-S01 strain (B), a composition containing hyaluronic acid (C), and a composition containing the LPC-S01 strain and hyaluronic acid (D), marked with hematoxylin-eosin staining, 24 hours after UV injury. [Figure 6a-d] Figures 6a, 6b, 6c, and 6d are images obtained under a microscope of histomorphometric analysis by H&E staining in the homeostasis model at 24 hours (6a: NC at 24 hours, 6b: P3-i at 24 hours) and 48 hours (6c: NC at 48 hours, 6d: P3-i at 48 hours). [Figure 7] Figure 7 shows gene expression results (qRT-PCR) at 24 hours in the homeostasis model for P1-i, P2-i, and P3-i products (RQ calculated using NC at 24 hours = 1; RQ<0.5 deregulation, RQ>2 upregulation). [Figure 8] FIG. 8 is a pretreatment protocol for UV irradiation of "scratched" tissue with a composition of the invention containing an inactivated strain. [Figure 9] FIG. 9 is a post-treatment protocol for UV irradiation of "scratched" tissue with a composition of the invention containing inactivated strains. [Figure 10-11] Figures 10 and 11 show the reduction in viability of the pathogen C. acnes DMS1897 expressed in Log10 CFU on skin inserts in vitro under experimental conditions (exclusion model and competition model, respectively). DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0022] definition In the context of the present invention, the term "skin" is used to denote the first line of defense with respect to the external environment; in particular, the defense is initiated by the action of keratinocytes scattered in the outer skin layer (epidermis), which induce the secretion of cytokines and chemokines to convey warning messages to deeper layers of the skin and cause an inflammatory response.

[0023] In the context of the present invention, the expression "skin ageing" is used to denote an irreversible evolutionary process; it is represented by a series of physiological changes that determine the loss of hydration of the skin, the appearance of microwrinkles, the loss of elasticity, hyperkeratosis and the formation of hyperpigmented spots called "senile freckles".

[0024] In the context of the present invention, the term "probiotics" is used to indicate according to the definition given by FAO and WHO: "live microorganisms which, when administered in adequate amounts, confer a health benefit on the host." In other words, probiotics are microorganisms (bacterial strains) which, when ingested in adequate amounts, demonstrate the ability to exert a beneficial function on the organism.

[0025] In the context of the present invention, the expression "hyaluronic acid" is used to denote a glycosaminoglycan consisting of repeating units of glucosamine and glucuronic acid linked together or by glycosidic bonds β1→4 and β1→3, and by intramolecular hydrogen bonds that stabilize its conformation.

[0026] Detailed Description of the Invention The object of the present invention is a mixture M comprising or consisting of (I) a bacterial strain belonging to the species Lactobacillus paracasei identified and deposited as Lactobacillus paracasei LPC-S01 DSM 26760 (live and viable or inactivated or derivatives thereof) and hyaluronic acid or a salt thereof; and (II) a composition (in short, the composition or compositions of the present invention) comprising at least one acceptable pharmaceutical or cosmetic or food grade additive and / or excipient.

[0027] The object of the present invention is also a composition or mixture M of the invention comprising or consisting of a bacterial strain belonging to the species Lactobacillus paracasei identified and deposited as L. paracasei LPC-S01 DMS 26760 and hyaluronic acid or a salt thereof (according to any of the described embodiments), for use as a medicament.

[0028] A first aspect of the present invention relates to a composition (composition of the invention) comprising a probiotic (L. paracasei LPC-S01 DSM 26760, viable or inactivated or a derivative thereof), preferably a probiotic bacterium, and hyaluronic acid or a salt thereof, for use in the treatment (therapeutic or cosmetic), prevention or alleviation of at least one sign or symptom associated with or caused by skin ageing (intrinsic ageing or extrinsic ageing as defined below).

[0029] Said signs or symptoms of skin ageing are generally associated with a series of alterations leading to a thinning and / or yielding of the skin structure.

[0030] Preferably, said aging is intrinsic or chronological aging, which depends substantially on genetic (or intrinsic) factors.Intrinsic aging generally begins after the age of 25.Preferably, said signs or symptoms related to or caused by intrinsic skin aging are selected from wrinkles, skin laxity, loss or deterioration of skin integrity, loss of skin elasticity, loss of skin firmness, skin thinning, skin scaling and skin dehydration, formation of dark spots or hyperpigmentation of skin, also called "age spots".

[0031] An object of the present invention is therefore the cosmetic use of a bacterial strain belonging to the species Lactobacillus paracasei identified and deposited as L. paracasei LPC-S01 DMS 26760 and hyaluronic acid or a salt thereof, and a composition or mixture M according to the invention, optionally comprising or consisting of a first substance and / or a second substance (according to any of the described embodiments), for the maintenance of skin homeostasis and / or as an anti-aging agent for the skin, for example for the cosmetic treatment of skin wrinkles, loss of skin elasticity (solar elastosis), dry or dry skin, rough skin, photoaging, redness of the skin, the presence of dilated capillaries on the cheeks, nose and / or ears, sunburn, abnormal or uneven pigmentation or hyperpigmentation, or to make the skin brighter and more natural.

[0032] Alternatively, the skin aging is extrinsic, i.e., due to external environmental factors (external factors).Extrinsic aging is caused by environmental factors such as, for example, attack of external factors and / or UV radiation (cause of photoaging), tobacco smoking, alcohol abuse, pollution, continuous contact with irritants, cold, wind and combinations thereof.Photoaging is particularly interesting in that it is associated with many diseases and skin damage that can lead to serious diseases such as skin tumors.

[0033] Preferably, said signs or symptoms associated with or caused by extrinsic skin ageing are selected from among erythema, photopigmentation or tanning, keratosis, preferably hyperkeratosis, skin redness, sunburn, burns, photoaging, solar elastosis, cortical cataract, pterygium, reactivation of cold sores, skin lesions of any nature (ulcers, wounds or bruises), preferably lip and / or conjunctival lesions, cutaneous melanoma, squamous epidermoid carcinoma, basal cell carcinoma (basal cell tumor), squamous epidermoid carcinoma or conjunctival carcinoma.

[0034] Skin ageing is inevitably associated with changes in the structure of the skin leading to an increased susceptibility to inflammatory and / or infectious diseases.

[0035] In one embodiment, a composition (composition of the present invention) comprising probiotics (L. paracasei LPC-S01 DSM 26760, viable or inactivated or derivatives thereof), preferably probiotic bacteria, and hyaluronic acid or a salt thereof for is used to treat (therapeutic treatment method), prevent or alleviate at least one sign or symptom associated with or caused by a weakened immune system of the skin or an inflammatory disease and / or a skin infection. In other words, the composition is used to strengthen the immune defense of the skin.

[0036] The at least one sign or symptom associated with or caused by a weakening of the skin's immune defenses or caused by an inflammatory condition of the skin is preferably selected from among dermatitis with irritation or abrasion, acne, acute or chronic dermatoses (e.g. rosacea or couperosa), skin infections, skin inflammation, erythema, ulcers, psoriasis, atopic dermatitis, otitis, cracks, fistulas and hemorrhoids.

[0037] Skin affections or diseases can be associated with or caused by pathogens, which can be bacteria, fungi, yeasts, viruses, and combinations thereof.

[0038] In one embodiment, the composition or mixture M of the invention comprising a probiotic (L. paracasei LPC-S01 DSM 26760, viable or inactivated or a derivative thereof) and hyaluronic acid or a salt thereof is used for example to treat (therapeutic treatment method), prevent or alleviate at least one sign or symptom associated with or caused by a pathogen.

[0039] Preferably, the pathogen is a bacterium, preferably a bacterium of the genus Propionibacterium, preferably acnes (species Propionibacterium acnes or Cutibacterium acnes, abbreviated C. acnes); Staphylococcus, preferably Staphylococcus epidermidis, Staphylococcus aureus, Staphylococcus warneri, Staphylococcus pyogenes, Staphylococcus mitis; Corynebacterium subsp.; Pseudomonas, preferably Pseudomonas aeruginosa; Acinetobacter, preferably Acinetobacter johnsonii; Streptococcus, preferably Streptococcus pyogenes; Micrococcus subsp., Brevibacterium subsp.

[0040] Experimental data prepared by the Applicant show that the composition or mixture M of the invention comprising hyaluronic acid and a probiotic (L. paracasei LPC-S01 DSM 26760, live and viable or inactivated or its derivatives) is capable of exerting an anti-inflammatory and / or immunomodulatory effect at the level of the keratinocytes and thus the skin.

[0041] Without wishing to be bound by any theory, the use of the composition is due to the anti-inflammatory capabilities, immune modulation, epidermal cell regeneration, epidermal differentiation, and enhanced skin structure favored by probiotics, as well as the hyaluronic acid contained in the composition.

[0042] In particular, the applicant has shown that when the skin is exposed to a composition containing hyaluronic acid and probiotics, it is possible to increase the differentiation process of the epidermis, in particular the stratum corneum thickening, and the collagen fibers are observed to be denser and more compact.

[0043] Furthermore, as evidenced by the evaluation of the expression of chemokine and defensin coding genes, the inventive composition comprising a probiotic ((L. paracasei LPC-S01 DSM 26760, viable or inactivated or a derivative thereof) and hyaluronic acid or a salt thereof is able to exert an immunomodulatory (or immunostimulatory) effect on the skin's immune system. In particular, an increase in the expression of defensin β2 has been observed both with the probiotic and with the inventive composition comprising hyaluronic acid and a probiotic.

[0044] In an embodiment of the invention, the probiotic (present in the composition of the invention together with the hyaluronic acid or its salts) is preferably a bacterium, a fungus, a yeast and combinations thereof; preferably a bacterium, more preferably a bacterial strain belonging to the species Lactobacillus paracasei and identified as L. paracasei LPC-S01 DSM 26760 (live, inactivated or derivatives thereof):

[0045] According to a preferred embodiment of the invention, the bacterium belongs to at least one genus selected from among Lactobacillus, Bifidobacterium, Bacillus, Propionibacterium, Streptococcus, Lactococcus, Aerococcus and Enterococcus.

[0046] More preferably, the bacterium belongs to the genus Lactobacillus.

[0047] According to a further preferred embodiment of the present invention, the bacteria of the genus Lactobacillus are Lactobacillus paracasei, Lactobacillus acidophilus, Lactobacillus amylolyticus, Lactobacillus amylovorus, Lactobacillus alimentarius, Lactobacillus avialis, Lactobacillus brevis, Lactobacillus buchneri, Lactobacillus casei, Lactobacillus cellobiosus, Lactobacillus coliniformis, Lactobacillus crispatus, Lactobacillus culbatus, Lactobacillus delbrueckii, Lactobacillus farciminis, Lactobacillus fermentum, Lactobacillus gallinarum, Lactobacillus spp. and at least one of the species selected from Lactobacillus gasseri, Lactobacillus helveticus, Lactobacillus hilgardii, Lactobacillus johnsonii, Lactobacillus kefiranofaciens, Lactobacillus kefiri, Lactobacillus mucosa, Lactobacillus panis, Lactobacillus corinoides, Lactobacillus paraplantarum, Lactobacillus pentosus, Lactobacillus plantarum, Lactobacillus pontis, Lactobacillus reuteri, Lactobacillus rhamnosus, Lactobacillus sakei, Lactobacillus salivarius, Lactobacillus sanfrancisensis, and combinations thereof.

[0048] More preferably, the lactic acid bacteria are of the species Lactobacillus paracasei, preferably of the strain Lactobacillus paracasei DG® CNCM I-1572 and / or the strain Lactobacillus paracasei LPC-S01 DSM26760.

[0049] Both strains were isolated and deposited by SOFAR SpA; in particular, the bacterial strain L. casei DG® (a trademark registered by Sofar, Italy) was deposited by SOFAR SpA at the National Collection of Microbial Cultures of the Institut Pasteur in Paris on May 5, 1995, under the accession number CNCMI-1572. Initially, the name of this strain was Lactobacillus casei DG subsp. casei (it has since been reclassified as Lactobacillus paracasei DG® CNCM I-1572).

[0050] The bacterial strain Lactobacillus paracasei LPC-S01 was deposited at the German Collection of Microbial Cell Cultures by SOFAR SpA under the accession number DSM26760 on 15 May 2017 (date of application for modification of the deposit under the Budapest Treaty; original date of deposit 11 January 2013).

[0051] Lactobacillus paracasei strains have been reclassified as Lacticaceibacillus paracasei.

[0052] In a preferred embodiment of the invention, the composition comprises Lactobacillus paracasei LPC-S01 and hyaluronic acid or a salt thereof.

[0053] According to a further preferred embodiment of the present invention, the bacterium of the genus Bifidobacterium is selected from the group consisting of B. animalis, B. bifidum, B. breve, B. infantis, B. longum, B. adolescentis, B. catenulatum, B. angulatum, B. asteroides, B. boum, B. coelinum, B. coryneforme, B. cuniculi, B. denticollens, B. dentium, B. gallicum, B. gallinarum, B. indicum, B. inopinatum, B. lactis, B. magnum, B. mericicum, B. minimum, B. pseudocatenulatum, B. pseudolongum, B. prolum, B. ruminantium, B. saeculare, B. subtilis, B. thermoacidophilum, B. thermophilum, B. more preferably, the bacterium belongs to at least one species selected from among Bacillus clausii, Bacillus subtilis, Bacillus coagulans, Bacillus megaterium, Bacillus halodurans, Bacillus thuringiensis, Bacillus insolitus, and Bacillus marinus.

[0054] According to a further preferred embodiment of the present invention, the bacterium of the genus Propionibacterium belongs to at least one species selected from among P. schermanii, P. acnes, P. australiens, P. avidum, P. cyclohexanicum, P. freudenreichii, P. granulosum, P. jensenii, P. microaerophyllum, P. propionicum and P. soenii.

[0055] According to a further preferred embodiment of the present invention, the bacterium of the genus Streptococcus is selected from the group consisting of Streptococcus thermophilus, Streptococcus salivarius, Streptococcus agalactiae, Streptococcus anginosus, Streptococcus bovis, Streptococcus canis, Streptococcus constellatus, Streptococcus downei, Streptococcus dysgalactiae, Streptococcus equinus, Streptococcus ferus, Streptococcus infantarius, Streptococcus iniae, Streptococcus intermedius, Streptococcus milleri, Streptococcus mitis, and Streptococcus spp. The strain belongs to at least one species selected from among Tococcus mutans, Streptococcus oralis, Streptococcus ollistii, Streptococcus parasanguinis, Streptococcus perolis, Streptococcus pneumoniae, Streptococcus pseudopneumoniae, Streptococcus pyogenes, Streptococcus lachi, Streptococcus tigrinus, Streptococcus sanguinis, Streptococcus sobrinus, Streptococcus suis, Streptococcus uberis, Streptococcus bestibularis, Streptococcus viridans and Streptococcus zooepidemicus.

[0056] According to a further preferred embodiment of the present invention, the bacterium of the genus Lactococcus belongs to at least one species selected from among L. chungangensis, L. formosensis, L. fujiensis, L. garvieae, L. lactis, L. pythium, L. plantarum, L. raffinolactis and L. taiwanensis.

[0057] According to a further preferred embodiment of the invention, the bacterium of the genus Aerococcus belongs to at least one species selected from among A. urinae, A. sanguinicola, A. christensenii, A. suis, A. urinaequi and A. urinaehominis.

[0058] According to a further preferred embodiment of the present invention, the bacteria of the genus Enterococcus belong to at least one species selected from among Enterococcus avium, Enterococcus durans, Enterococcus faecalis, Enterococcus faecium, Enterococcus gallinarum, Enterococcus hemoperoxidus, Enterococcus hirae, Enterococcus malodoratus, Enterococcus moraviensis, Enterococcus mundtii, Enterococcus pseudoavium, Enterococcus raffinosus and Enterococcus solitarius.

[0059] According to a further preferred embodiment of the invention, the yeast fungus belongs to the genus Saccharomyces, more preferably to the species Saccharomyces cerevisiae and / or Saccharomyces boulardii.

[0060] In the mixtures or compositions of the present invention, the probiotics, preferably the bacterial strain L. casei DG® CNCM I-1572 and / or the bacterial strain Lactobacillus paracasei LPC-S01 DSM 26760, are used alive (together with hyaluronic acid or a salt thereof), i.e. they are used as probiotics.

[0061] Alternatively, said probiotics, preferably the bacterial strain L. casei DG® CNCM I-1572 and / or the bacterial strain Lactobacillus paracasei LPC-S01 DSM 26760, are dead and / or inactivated and / or tyndallized.

[0062] For example, viable strains (probiotics) of the invention (e.g. L. paracasei LPC-S01 DSM 26760) can be inactivated by heating or tindalization or gamma irradiation or sonication. Said inactivation by heating or tindalization can be carried out at a temperature ranging from 50°C to 120°C, preferably from 65°C to 105°C, more preferably from 75°C to 95°C, e.g. at about 85°C, for a time period comprised in the range of 30 minutes to 120 minutes, preferably from 45 minutes to 85 minutes, e.g. for about 60 minutes; or by tindalization. The heating or tindalization or gamma irradiation or sonication process is carried out according to techniques, procedures and equipment known to the skilled person.

[0063] Bacteria subjected to the inactivation process by heating or tindalization have cell walls that remain intact but are dead (control by plate counts and / or cytofluorometry) with a percentage of bacteria ranging from 70% to 99.5%, preferably 80% to 95%, with respect to the total number of bacteria subjected to the heating or tindalization inactivation technique.

[0064] In a further embodiment, the probiotics, preferably the bacterial strain L. casei DG® CNCM I-1572 and / or the bacterial strain Lactobacillus paracasei LPC-S01 DSM 26760, are used in the form of a lysate and / or extract (together with hyaluronic acid or a salt thereof), i.e. they are used as paraprobiotics.

[0065] Alternatively, said probiotics, preferably the bacterial strain L. casei DG® CNCM I-1572 and / or the bacterial strain Actobacillus paracasei LPC-S01 DSM 26760, are used (together with hyaluronic acid or a salt thereof) in the form of bacterial products selected among the supernatant, metabolites, biological products, postbiotics, cell walls and their components, exopolysaccharides, ribosomes and glycoproteins, glucans and other polysaccharides, lipopolysaccharides and any components of the supernatant.

[0066] In short, in the context of the present invention, the expression "derivatives" of a bacterial strain or a viable bacterial strain (e.g. L. paracasei LPC-S01 DSM 26760) or a probiotic is any derivative and / or component (supernatant, metabolites, biological products, postbiotics, cell walls and their components, exopolysaccharides, ribosomes and glycoproteins, glucans and other polysaccharides, lipopolysaccharides and any component of the supernatant) of said paraprobiotic or bacterial strain, which, when administered in an appropriate amount (via oral or topical route), confers a benefit to the human or animal consumer.

[0067] In the context of the present invention, the term "probiotics" denotes and includes, unless otherwise specified, live and inactivated bacterial strains as defined above (e.g. L. paracasei LPC-S01 DSM 26760) and derivatives of said bacterial strains.

[0068] Generally, said probiotics are single microorganisms or combinations or consortia of microorganisms of any of the microbial species listed in the EFSA QPS list.

[0069] Preferably, said composition comprises a combination of the above reported strains with other microorganisms as above, preferably selected from among bacteria, fungi, yeasts and combinations thereof.

[0070] The probiotic, preferably the bacterial strain L. casei DG® CNCM I-1572 and / or the bacterial strain Lactobacillus paracasei LPC-S01 DSM 26760, is present in the composition (together with hyaluronic acid or a salt thereof) in a minimal amount sufficient to allow the temporary colonization of the skin, intestine and / or other areas of the organism. Preferably, for a daily intake (or single administration) of the composition of the invention, said amount is greater than or equal to 1x10 6 CFU~1x10 12 CFU range, preferably 10 8~10 12 Units of Microbiology, 10 8 ~10 12 units of microorganisms, more preferably 10 9 ~10 11 Units of microorganisms, for example, about 1x10 9 It varies at concentrations in the range of CFU (colony forming units) and above.

[0071] The probiotics of the present invention, preferably the bacterial strain L. casei DG® CNCM I-1572 and / or the bacterial strain Lactobacillus paracasei LPC-S01 DSM 26760, are preferably administered in a dose of 10 8 ~10 12 units of microorganisms, more preferably 10 9 ~10 11 It is administered in amounts that vary between units of microorganisms.

[0072] According to a preferred embodiment, probiotics and bacteria are preferably taken at least once or twice a day.

[0073] As mentioned above, the composition or mixture M of the present invention comprises hyaluronic acid or its salts, as well as combinations thereof. Said hyaluronic acid or its salts (abbreviated as HA) is comprised in the composition of the present invention together with the L. paracasei LPC-S01 DMS 26760 strain and optionally at least one further first or second substance (according to any of the described embodiments), and preferably has a molecular weight of about 10 kDa (kilodalton = 1,000.00 Daltons or 10 3The hyaluronate has an average molecular weight in the range of about 1,000 kDa to 2,000 kDa (Daltons), preferably about 800 kDa to 2,500 kDa, more preferably about 1,000 kDa to 2,000 kDa, for example, about 1,300 kDa, 1,400 kDa, 1,500 kDa, 1,600 kDa, 1,700 kDa, 1,800 kDa. In one embodiment, the hyaluronate (e.g., an alkali or alkaline earth metal hyaluronate) is selected from sodium hyaluronate, potassium hyaluronate, ammonium hyaluronate, calcium hyaluronate, magnesium hyaluronate, zinc hyaluronate, cobalt hyaluronate, and combinations thereof.

[0074] Furthermore, in the context of the present invention, the terms "hyaluronic acid or its salts" or "HA" or simply "hyaluronic acid" are used to denote hyaluronic acid per se, as well as hydrolyzed hyaluronic acid (obtained, for example, by fermentation), and the hyaluronate salts (hyaluronates) described above.

[0075] When said hyaluronic acid of the present invention is a biotechnologically hydrolyzed hyaluronic acid obtained by fermentation, it can have an average molecular weight of about 10 kDa.When said hyaluronic acid of the present invention is sodium hyaluronate (e.g., CAS number 9067-32-7, Mw-molecular weight 1,000-1,400 kDa or Mw1,000-1,700 kDa) or potassium hyaluronate, it can have an average molecular weight comprised in the range of about 1,000 kDa to 2,000 kDa.

[0076] In addition to L. paracasei LPC-01 DSM 26760 and HA, the compositions of the invention advantageously further comprise a pharma- ceutically acceptable excipient and / or further substance (e.g. a first substance or a second substance as described below) and / or a carrier.

[0077] In addition to L. paracasei LPC-01 DSM 26760 and HA, and optionally a second substance (defined below), the composition of the invention preferably further comprises a first substance selected from among plasma, PRP, a cicatrizing substance, a re-epithelializing substance, a humectant, a hydrating agent, an emollient, an adsorbent, an analgesic, a phlebotonic, an anti-inflammatory agent, a muscle relaxant, an antibiotic, an antibacterial agent, an antifungal agent, an antiviral agent, an insecticide, a peptide and / or protein substance and / or a protein such as collagen, a substance belonging to connective tissue such as glycosaminoglycans, preferably chondroitin sulfate, and / or a combination thereof.

[0078] In one embodiment of the invention, the composition is formulated for topical or dermatologic application (e.g., in solid, semi-solid or liquid form), preferably in the form of a cream, gel, oil, emulsion (or foam), solution, dispersion (solid-liquid or liquid-liquid), suspension, two-phase mixture, spray (spray liquid), gauze, plaster, bandage, lotion, mousse, mask (mask that can be applied to the skin), ointment or paste.

[0079] In one embodiment of the invention, the composition is formulated for oral administration, preferably as a tablet, capsule, bar, granule powder, operculum, buccal soluble granules, sachet or pill, suspension (e.g. drinkable vial) or solution (monophasic or biphasic).

[0080] Alternatively, the composition is prepared extemporaneously by mixing the composition with water.

[0081] Alternatively, for example, for the preparation of a mask to be applied to the skin or a suspension for oral use (drinkable vial), the composition is extemporaneously prepared by mixing together two components, probiotics (L. paracasei LPC-01 DSM 26760) and hyaluronic acid or a salt thereof. In particular, the device for extemporaneous preparation of the composition of the present invention may consist of a vial containing an aqueous solution of hyaluronic acid or a salt thereof and a part of one end of a bottle (e.g., a cap, for sealing the vial) containing the bacterial strain therein (L. paracasei LPC-01 DSM 26760, viable or inactivated or its derivatives) in solid form of powder, granules or tablets; the extemporaneous preparation of the composition of the present invention occurs by releasing (e.g., by pressure) the bacterial strain in solid form from the end of the vial into the solution of hyaluronic acid or a salt thereof contained in the vial.

[0082] According to a preferred embodiment, in addition to L. paracasei LPC-01 DSM 26760 and HA, and optionally said first substance, the composition of the invention comprises other substances (second substances) selected from among amino acids, supplements, vitamins, trace elements such as zinc and selenium, macro- and micronutrients, enzymes and / or prebiotic substances such as fructooligosaccharides (FOS), galactooligosaccharides (GOS), xylooligosaccharides (XOS), inulin, guar gum or combinations thereof.

[0083] The composition of the present invention, comprising L. paracasei LPC-01 DSM 26760, HA, and optionally a first or second substance, further comprises said (II) at least one pharmaceutical or food or cosmetic grade additive and / or excipient, which is a substance lacking therapeutic activity suitable for pharmaceuticals or foods. In the context of the present invention, additives and / or excipients acceptable for pharmaceutical or food or cosmetic use include all auxiliary substances known to those skilled in the art for preparing compositions in solid, semi-solid or liquid form, such as, for example, diluents, solvents (such as water, glycerin, ethyl alcohol), solubilizers, acidifiers, thickeners, sweeteners, flavor enhancers, colorants, lubricants, surfactants, preservatives, pH stabilizing buffers and mixtures thereof.

[0084] The composition of the present invention comprising L. paracasei strain LPC-S01 DMS 26760 and hyaluronic acid or a salt thereof, and optionally a first and / or second substance, may be a pharmaceutical composition (or live biotherapeutic product), a medical device composition, a dietary supplement, a food, a novel food, a probiotic product, a composition for foods for special medical purposes (FSMP), or a cosmetic composition.

[0085] An embodiment (FRn) of the present invention is outlined below: FR1. A composition comprising a probiotic and hyaluronic acid or a salt thereof for use in the treatment, prevention or alleviation of at least one sign or symptom associated with / caused by aging of the skin or in the treatment, prevention or alleviation of at least one sign or symptom associated with / caused by a weakened immune system of the skin. FR2. A composition for use according to FR1, wherein skin aging is selected from among intrinsic skin aging and extrinsic skin aging. FR3. The composition according to FR2, wherein at least one sign or symptom associated with / caused by intrinsic skin aging is selected from among wrinkles, sagging skin, loss or deterioration of skin integrity, lack of skin elasticity, lack of skin tone, thinning skin, peeling skin and dehydration of skin. FR4. A composition for use according to FR2, wherein at least one sign or symptom associated with / or caused by extrinsic skin aging is selected from among erythema, pigmentation, keratosis, preferably hyperkeratosis, skin redness, burns, cortical cataracts, pterygium, reactivation of cold sores, skin lesions of any nature, preferably lip and / or conjunctival lesions, cutaneous melanoma, cutaneous squamous epidermoid carcinoma, basal cell carcinoma (basal cell tumor), corneal or conjunctival squamous epidermoid carcinoma. FR5. A composition for use according to FR1, wherein the at least one sign or symptom associated with / or caused by a weakened immune system of the skin is selected from among dermatitis, preferably with irritation or abrasion, acne, infections, inflammation of the skin, erythema, ulcers, psoriasis, atopic dermatitis, otitis, cracks, fistulas and hemorrhoids. FR6. A composition for use according to any one of FR1 to 5, wherein said probiotic is preferably selected among bacteria, fungi, yeasts and combinations thereof, preferably a bacterium belonging to at least one genus selected among Lactobacillus, Bifidobacterium, Bacillus, Propionibacterium, Streptococcus, Lactococcus, Aerococcus and Enterococcus. FR7. Bacteria of the genus Lactobacillus include Lactobacillus paracasei, Lactobacillus acidophilus, Lactobacillus amylolyticus, Lactobacillus amylovorus, Lactobacillus alimentarius, Lactobacillus avialis, Lactobacillus brevis, Lactobacillus buchneri, Lactobacillus casei, Lactobacillus cellobiosus, Lactobacillus coliniformis, Lactobacillus crispatus, Lactobacillus carbatus, Lactobacillus delbrueckii, Lactobacillus farciminis, Lactobacillus fermentum, Lactobacillus gallinarum, Lactobacillus gasseri, Lactobacillus The composition for use according to FR6, wherein the Lactobacillus subtilis belongs to at least one species selected from among Lactobacillus helveticus, Lactobacillus hilgardii, Lactobacillus johnsonii, Lactobacillus kefiranofaciens, Lactobacillus kefiri, Lactobacillus mucosa, Lactobacillus panis, Lactobacillus corinoides, Lactobacillus paraplantarum, Lactobacillus pentosus, Lactobacillus plantarum, Lactobacillus pontis, Lactobacillus reuteri, Lactobacillus rhamnosus, Lactobacillus sakei, Lactobacillus salivarius, Lactobacillus sanfrancisensis and combinations thereof. FR8. A composition for use according to FR6 or FR7, wherein the bacteria is of the Lactobacillus paracasei species, preferably of the Lactobacillus paracasei DG® strain CNCM I-1572 and / or the Lactobacillus paracasei strain LPC-S01 DSM 26760. FR9. The composition for use according to any one of the preceding FRs, wherein the hyaluronate salt is selected from among sodium hyaluronate, potassium hyaluronate, ammonium hyaluronate, calcium hyaluronate, magnesium hyaluronate, zinc hyaluronate, cobalt hyaluronate, and combinations thereof. FR10. A composition for use according to any one of the preceding FRs, wherein said probiotic is live, and / or dead, and / or inactivated, and / or tindalized, and / or in the form of a lysate and / or extract, and / or in the form of a bacterial product selected from supernatant, metabolites, biological products, postbiotics, cell walls and their components, exopolysaccharides, ribosomes and glycoproteins, glucans and other polysaccharides, lipopolysaccharides and any component of the supernatant. FR11. The probiotic comprises: 8 ~10 12 units of microorganisms, preferably 10 9 ~10 11 A composition for use according to any one of the preceding FRs, wherein the microorganisms are present in variable amounts among the units. FR12. Compositions for use in accordance with any of the preceding FRs in the form of a cream, gel, oil, emulsion, spray, gauze, plaster, bandage, lotion, mousse, mask, ointment, paste, or liquid formulation for extemporaneous preparation.

[0086] The terms "treatment" or "therapeutic treatment" or "therapeutic method" in the context of the present invention are used to indicate an intervention in a subject in need thereof, including administration of a therapeutically effective amount of composition or mixture M, for the purpose of eliminating, alleviating / reducing or preventing a condition or disease and its symptoms or disorders.

[0087] The term "therapeutically effective amount" refers to that amount of active compound and / or bacterial strain that elicits a biological or medical response in a tissue, system, mammal, or human that is desired and defined by an individual, researcher, veterinarian, physician, or other clinician or health care professional.

[0088] In the context of the present invention, the expression "subject" is used to indicate a human subject or an animal subject (e.g. a pet such as a dog or cat or other mammal). Preferably, the compositions of the present invention are for use in a method of medical treatment or for cosmetic use in human subjects.

[0089] In the context of the present invention, the term "medical device" is used in the sense according to Legislative Decree No. 46 of 24 February 1997 or according to the new Medical Device Regulation (EU) 2017 / 745 (MDR).

[0090] In the context of the present invention, the term "novel food" is used in the sense according to Regulation EC258 of 1997.

[0091] Unless otherwise specified, an expression composition or mixture or other containing an amount of a component "ranging from x to y" is used to indicate that said component may be present in the composition or mixture or extract or other in any amount that is present in the end ranges of the included range, even if not specified. EXAMPLES

[0092] Example A A cream according to the invention comprising the L. paracasei LPC-S01 DMS 26760 strain and hyaluronic acid or a salt thereof: To prepare the cream, strain LPC-S01 DSM 26760 (viable or inactivated) - powder or powder capsules (approximately 8x10 9 The lyophilized cells in the form of colony-forming units (CFU) were dissolved in 13 ml of hyaluronic acid-based cream (abbreviated as HA cream).

[0093] Example of HA cream composition (w / w%): - Water (solvent) qs to 100%; - Functional substances: Octocrylene (UV-B filter) 2-8% (4.5%), BMDBM stabilized with Octocrylene (UV-B filter) 0.1-5% (2%) in capsules, Shea organic butter (butyrospermum parkii = shea) (CAS number 194043-92-0) 0.1-4% (1%), collagen complex and panthenol 0.1-4% (1%), butyl methoxydibenzoylmethane (UV-A filter) 0.1-4% (1%), vitamin E 0.01-1% (0.3%), gardenia stem 0.01-1% (0.1%), low molecular weight hyaluronic acid (for example, CAS number 9004-61-9) 0.005-1% (0.05%), medium / high molecular weight hyaluronic acid (for example, CAS number 9067-32-7) 0.005-1%(0.02%); - excipients and additives (2-10% w / w, depending on the technical requirements known to the skilled person): antioxidants (e.g. tocopheryl acetate), preservatives (e.g. phenoxyethanol, potassium sorbate), surfactant-emulsifiers (e.g. cetearyl glucoside, cetyl alcohol), emulsion stabilizers (e.g. carbomer), solvents (e.g. 1,2-hexanediol), abrasives (e.g. silica), binders (e.g. PVP), moisturizers (e.g. glycerin) and / or skin conditioning agents (e.g. dimethicone, xanthan gum, tropolone).

[0094] Example B A pack according to the invention comprising the L. paracasei LPC-S01 DMS 26760 strain and hyaluronic acid or a salt thereof: To prepare the pack, strain LPC-S01 DSM 26760 (viable or inactivated, preferably viable)-powder or powder capsules (approximately 8x10 9 Aqueous solutions of hyaluronic acid or its salts, for example solutions having the components set out in Table A, are prepared by lyophilization in the form of a hyaluronic acid solution containing hyaluronic acid or its salts, for example solutions having the components set out in Table A. wherein 0.01-2% (0.1%) of low molecular weight hyaluronic acid (e.g., CAS number 9004-61-9) and 0.005-1% (0.05%) of medium / high molecular weight hyaluronic acid (e.g., CAS number 9067-32-7) are present in a weight / weight percentage (based on the total weight of the aqueous hyaluronic acid solution). Table A [Table 1]

[0095] - Heat inactivated L. paracasei strain LPC-S01 DMS 26760:

[0096] Experimental Part-(1) Episkin T-Skin TM Model (3D skin model) Episkin T-Skin TM (abbreviated as T-Skin or "full thickness skin" or 3D skin) is an in vitro reconstructed 3D skin model that includes the dermis and epidermis (full thickness skin model). Episkin T-Skin TM is an in vitro reconstructed skin consisting of a human fibroblast-equivalent dermis overlaid on a well-differentiated stratified epidermis derived from normal human keratinocytes cultured on an inert polycarbonate filter. In vitro reconstructed human skin models are close to in vivo human tissue in terms of morphology (multilayered epidermis), biochemical and physiological properties and are currently the most promising alternative to animals, ex vivo explants and submerged cell monolayers for the evaluation of the efficacy and safety of topical application of products (Gordon et al. 2015, Zuang V. 2016).

[0097] The biological relevance and predictability of these models derives from the presence of tissues organized with different layers of living cells, which allows to evaluate topically applied products at realistic clinical doses and exposure conditions. Treatment of human skin with topically applied products, such as cosmetics, results in a genomic response with dynamic pathways, which represent, at the transcriptional level, the first cellular signal involved in a series of events. 3D human tissues are relevant test systems to study mechanisms of action and evaluate the efficacy of products, taking into account both the direct genomic response and the consequences of cellular and crosstalk communication via the expression of soluble mediators and specific biomarkers.

[0098] I. Episkin T-Skin TM Homeostasis model (non-inflammatory) Episkin T-Skin TM In the present in vitro study of a homeostasis model, the effectiveness of a composition according to the invention comprising hyaluronic acid (HA) and viable or inactivated bacterial strain LPC-S01 DSM 26760 in terms of benefits on skin homeostasis was evaluated to investigate its potential applications and effectiveness for skin care.

[0099] The objective of the study was to study the skin tolerance profile of compositions according to the invention after exposure to high concentrations and to evaluate their effectiveness in: - Strengthening the skin's self-defense by inducing antibacterial peptides, Stimulation of innate immune responses of keratinocytes, epidermal regeneration and differentiation Induction of positive renewal of the epidermal and dermal compartments, acting as an anti-aging agent.

[0100] I.1. Viable strains - homeostasis model I.1.1. Products and Controls Under Analysis - Negative control (NC): 0.9% NaCl saline; - P1: viable strain LPC-S01 DSM 26760 resuspended in saline; - P2: hyaluronic acid based aqueous solution (as in Example B (pack) above); - P3: viable strain LPC-S01 DSM 26760 resuspended in hyaluronic acid-based aqueous solution;

[0101] To prepare P3, freeze-dried powder capsules of viable strain LPC-S01 DSM 26760 (approximately 8 × 10 9 The contents of each of the 1000 cells / ml of hyaluronic acid-based aqueous solution were dissolved in 13 ml of the solution. To prepare P1 (strain only), freeze-dried powder capsules of viable strain LPC-S01 DSM 26760 (approximately 8 × 10 9 The contents of the culture (CFU) were resuspended in 13 ml of saline.

[0102] I.1.2. Methodological evaluation of self-defense and increased cell regeneration capacity In a complete 3D skin model reconstructed in vitro ("full thickness skin" model), which reproduces the dermal and epidermal compartments and thus allows studying the modification of the extracellular matrix of the dermis and the differentiation of the viable skin layers, we evaluated the increased self-defense and cell regeneration capacity of the probiotic strain LPC-S01 (viable) plus hyaluronic acid (P3) and the probiotic strain LPC-S01 (Lactobacillus paracasei LPC-S01 DSM 26760, viable; P1) in hyaluronic acid (P2).

[0103] This study focused on evaluating the effect of a composition containing the strain LPC-S01 DSM 26760, hyaluronic acid, and the LPC-S01 strain + hyaluronic acid on the activation of immune response, cell differentiation of the epidermis, and cell regeneration of the dermis. The composition containing the strain LPC-S01 DSM 26760, hyaluronic acid, and the LPC-S01 probiotic strain + hyaluronic acid was applied (30 μl) directly to the surface of the 3D skin model and incubated for 8 hours, after which it was rinsed using saline to eliminate excess product. The tissue was cultured for an additional 16 hours before analysis, mimicking a realistic exposure of the face pack at 24 hours. Saline was used as a negative control (NC).

[0104] The following parameters were analyzed with respect to the negative control (according to methods known to those skilled in the art): Histological analysis by Masson's trichrome staining; · Gene expression (qRT-PCR) of main biomarkers of skin defense (HBD2 and CCL27), innate immune response (TLR2), epidermal differentiation (KRT14, LOR and IVL), epidermal regeneration (HAS-2, CD44, collagen III, IV and XIII, KGF and EGF); · Cell damage by quantifying the release of adenylate kinase (AK for short) (Toxilight assay). Experiments were performed in biological triplicates.

[0105] I.1.2.1. Histomorphometric analysis by Masson's trichrome staining At the end of the treatment, tissues were washed with saline and fixed in 10% formalin. Histological sections were marked using a Masson's Trichrome Kit (Abcam 150686) according to the manufacturer's instructions. For each sample, three microscopic acquisitions were performed on three different parts of the section. Histological samples were analyzed under a light microscope (magnifications 20x and 40x) to evaluate morphological changes in the tissue.

[0106] I.1.2.2. Real-time PCR Analysis At the end of the treatment, tissues were harvested in lysis buffer for RNA extraction and cDNA reverse transcription. RNA integrity was assessed by loading the extracted RNA on a 1% agarose gel: 18S and 28S ribosomal bands were detected. GAPDH was used as an endogenous control gene to normalize the input amount. Analysis of the obtained data was performed using methods known to those skilled in the art.

[0107] I.1.3. Consequences of Activating Self-Defense and Cellular Regeneration Abilities I.1.3.1. Results of histomorphometric analysis using Masson's trichrome staining After incubation with saline, the negative control (Figure 1A) showed no morphological and / or structural changes in both the epidermis and dermis: the distribution of collagen fibers was oriented and contained fibroblasts.

[0108] Treatment with strain LPC-S01 DSM 26760 (viable) did not induce any significant changes in the structure of the epidermis and dermis. Collagen fibers and their distribution showed a decreased fiber thickness and density compared to the negative control (Figure 1B).

[0109] Treatment with hyaluronic acid did not induce any significant changes in the structure of the epidermis and dermis: collagen fibers showed a decreased density compared to the negative control (Figure 2A).

[0110] Treatment with the probiotic strain LPC-S01 DSM 26760 (viable) + hyaluronic acid was able to change the morphology of the epidermis, especially that of the thinner stratum corneum, and increased the differentiation process (Figure 2B).

[0111] I.1.3.2. Real-time PCR results (qRT-PCR) Table 1 shows the relative quantification (RQ) with respect to the negative control of the values ​​obtained by real-time PCR for tissues treated with LPC-S01 DSM 26760 (viable), hyaluronic acid and LPC-S01 DSM 26760 (viable) + hyaluronic acid.

[0112] Table 1 [Table 2]

[0113] Treatment with the probiotic LPC-S01 DSM 26760 induces an increase in human defensin beta2 (HBD2) and TLR2. These data are consistent with the immunomodulatory properties of the probiotic and demonstrate its ability to trigger skin defense and enhance the innate immune response in the skin.

[0114] Treatment with hyaluronic acid fails to induce modulation of the expression of the gene targets evaluated.

[0115] Treatment with hyaluronic acid + LPC-S01 DSM 26760 causes an increase in HBD2 expression compared to treatment with hyaluronic acid. A decrease in collagen III and HAS-2 levels was observed (as already observed with probiotic treatment alone), while a decrease in KGF was also observed.

[0116] Generally speaking, the results obtained show that the probiotic LPC-S01 DSM 26760, when applied alone, exerts a positive effect on the skin by enhancing innate immunity (based on TLR2 and HBD-2).

[0117] Hyaluronic acid applied alone does not exert any positive effect on the skin; on the contrary, LPC-S01 introduced in the same formulation as hyaluronic acid is able to maintain its main activity of enhancing the skin's natural defenses.

[0118] I.1.3.4. Adenylate kinase release results (Toxilight assay) The levels of adenylate kinase released by tissues treated with the products under study indicate good biocompatibility of the products after 8 and 16 hours of incubation.

[0119] I.1.4. Conclusion The results obtained show that treatment with hyaluronic acid + LPC-S01 DSM 26760 (viable and viable) is the most promising, showing a positive effect on improving the differentiation process of the skin, in skin regeneration and, usually, in strengthening the structure of the dermal compartment by increasing the collagen network. Thus, the combined administration of hyaluronic acid and the probiotic LPC-S01 DSM 26760 (P3) shows a synergistic effect in strengthening the dermal structure, intervening in a key factor of cell differentiation and regeneration. This synergistic effect was not predictable, since the separate administration of hyaluronic acid and the probiotic LPC-S01 DSM 26760 did not show any significant effect on skin differentiation.

[0120] I.2. Inactivated Bacterial Strains - Homeostasis Model I.2.1. Products and controls under analysis - Negative control (NC): 0.9% NaCl saline; - P1-i.: inactivated strain LPC-S01 DMS 26760 (10 9 cells / tissue), using a concentration of 2 g LPC-S01 / ml; - P2-i.: hyaluronic acid based cream (as in Example A (cream) above); - P3-i.: inactivated strain LPC-S01 DSM 26760 resuspended in hyaluronic acid based cream, using a concentration of 2 g cells / ml.

[0121] To prepare P3-i., freeze-dried powder capsules of inactivated strain LPC-S01 DSM 26760 (approximately 8 × 10 9 The contents of each CFU were dissolved in 13 ml of hyaluronic acid-based cream. To prepare P1-i. (strain only), freeze-dried powder capsules of inactivated strain LPC-S01 DSM 26760 (approximately 8 × 10 9 The contents of the cells (CFU) were resuspended in saline.

[0122] I.2.2. Inactivation of bacterial strains during analysis Starting material: 2×10 11 Viable cells of strain LPC-S01 DSM 26760 in lyophilized form with a viable cell count of cells / g powder. The day before treatment, 2 g of powder was weighed out and resuspended in 4 mL of saline. 11 A suspension of bacterial cells / mL of saline was obtained, and 30 μL of this suspension was used to confirm the effective bacterial load by counting on MRS agar.

[0123] On the day of treatment, a suspension of the strain prepared in saline was heat inactivated by incubating at 85°C for 1 h. After this period, the bacteria were transferred to four Eppendorf tubes (1 ml each, 10 11 The pellet was then resuspended in: - Obtain 1 ml of saline, P1-i. - Obtain 1ml of hyaluronic acid cream, P3-i.

[0124] I.2.3. Methodology The products under analysis and the negative control (P1-i., P2-i., P3-i., NC: 15 μl) were applied directly to the surface of the T-Skin model tissue for 24 and 48 h under homeostatic conditions. 9 bacteria / tissue was applied.

[0125] The following parameters were analyzed with respect to the untreated control (negative control, NC): · Histomorphological analysis by H&E (hematoxylin & eosin) staining; Gene expression of key biomarkers of skin defense (human defensin beta2 (DEFB4)), innate immune response (TLR2, TNFα), differentiation and epidermal regeneration (TGMS-1, CCND1, TGF-β1) by RT-qPCR. Experiments were performed in biological triplicates.

[0126] I.2.4. Results I.2.4.1. Results of H&E histomorphometric analysis at 24 and 48 hours Three sections (consisting of three replicates) of vertical tissue were prepared on each histological slide; five microscopic acquisitions were performed on selected sections. For each biological replicate, the most representative acquisition of the selected vertical sections is reported. The average thickness was calculated in the five microscopic acquisitions.

[0127] The results are reported below: CN at 24 hours (Figure 6a): - Epidermis: fully viable and with normal SC (stratum corneum) lamellar structure; - Dermal-epidermal junction: structural integrity is observed; - Distribution of fibres and collagen: oriented, contains many fibroblasts. P1-i. at 24 hours (not shown): - Epidermis: differences were observed in the same replicates, probably related to the uneven distribution; it is evident that many cells show metabolic activation and proliferation; there are few pyknotic nuclei; the SC lamellar structure does not appear to be significantly altered; P3-i at 24 h (Figure 6b): - Epidermis: differences were observed in the same replicates, probably related to the uneven distribution; it is evident that many cells show metabolic activation and proliferation; there are few pyknotic nuclei; the SC lamellar structure Significantly altered Looks like; - Dermal-epidermal junction: structural integrity is observed; - Distribution of fibres and collagen: dense, tightly packed and oriented, containing many fibroblasts.

[0128] NCs at 48 h (Figure 6c): - Epidermis: fully viable and with normal SC (stratum corneum) lamellar structure; - dermal-epidermal junction: delamination and loss of integrity (inherent fragility of tissues) were observed; - Distribution of fibres and collagen: oriented, contains many fibroblasts. P1-i. at 48 hours (not shown): - Epidermis: A fully differentiated epidermis is observed; the tissue shows altered SCs in terms of structure and thickness due to greater proliferation and differentiation. P3-i at 48 hours (Figure 6d): - Epidermis: differences were observed in the same replicates, probably related to an uneven distribution; many cells show metabolic activation and proliferation; few pyknotic nuclei; the SC (stratum corneum) lamellar structure appears altered due to greater proliferation; - Dermal-epidermal junction: structural integrity is observed; - Fiber and collagen distribution: oriented, contains many fibroblasts; denser and more tightly packed relative to the negative control.

[0129] The above data show that after application to P3-i tissues in 24 hours the lamellar structure of the SC (stratum corneum) appears to be altered, whereas, taking into account that after application of P1-i it is necessary to wait 48 hours before observing any changes in the SC lamellar structure, composition P3-i. (inactivated strains + HA) acts in a shorter time and with greater potency than composition P1-i (inactivated strains only).

[0130] I.2.4.2. Real-time PCR Results I.2.4.2.1. Real-time PCR results at 24 hours Figure 7 shows the results of gene expression (qRT-PCR) at 24 h (RQ calculated using NC at 24 h = 1; RQ < 0.5 deregulation, RQ > 2 upregulation).

[0131] The relative quantification (RQ) gene expression (qRT-PCR) results obtained in tissues treated for 24 hours with the compositions under analysis (P1-i., P2-i., P3-i.) are summarized below in Figure 7. The results are expressed with respect to the negative control (RQ=1 calculated using NC at 24 hours; RQ<0.5 deregulation, RQ>2 upregulation).

[0132] As a general consideration, the non-completely homogeneous application of the compositions under analysis resulted in high biological variability between the triplicates.

[0133] 24 hour post-treatment: The inactivated probiotic strains under analysis, alone (P1-i) or in compositions with HA (P3-i), induced an upregulation of human defensin β2 (DEFB4). These data are in line with the immunomodulatory properties of the viable strain LPC-S01 DMS 26760 observed in section I.1.3.1, showing its ability to induce skin defense even in a nonviable state. This immunomodulatory activity may therefore correlate with externally exposed elements within the bacterial cell wall. The composition containing only HA (P2-i.) did not modulate human defensin β2 (DEFB4): this result confirms that the upregulation of DEFB4 in P3-i. (strains + HA) is only related to the presence of bacteria. Composition P3-i. (strain + HA) induced an upregulation of human defensin beta 2 (DEFB4) in a higher (although not significant) manner at 24 hours compared to P1-i. (strain only). A significant modulation of TNFα was quantified, indicating an induction of an inflammatory response, possibly due to immune recognition of the bacteria by the skin surface. This result may be related to the high dose of LPC-S01 DMS 26760 strain contained in composition P3-i., since this effect is not observed in tissues treated with P2-i. (HA only).

[0134] I.2.4.2.2. Real-time PCR results at 48 hours The induction of human defensin β2 (DEFB4) by the inactivated bacterial strains under analysis (both P1-i. and P3-i.) was confirmed at values ​​higher than those at the 24 h time point (section I.2.4.2.1), indicating a stable biological response and an enhanced skin defense resulting in an effective protective mechanism.

[0135] I.2.5. Conclusion In a homeostatic (non-inflammatory) model, the composition according to the invention P3-i. (inactivated strain + HA), comprising a combination of inactivated LPC-S01 DMS 26760 strain and hyaluronic acid, was well tolerated in the 3D skin model and was able to stimulate the body's defense and cell differentiation processes compared to the individual components and / or the negative control.

[0136] In particular, the efficacy level of the composition of the invention P3-i. (inactivated strain+HA) is reached in a shorter time compared to the bacterial strain not combined with hyaluronic acid (P1-i.).

[0137] II.EpiskinT-Skin TM Inflammation models in models The ability of a composition according to the invention, comprising the bacterial strain LPC-S01 DMS 26760 (viable or inactivated) and hyaluronic acid, to reduce the damage caused by UV radiation was demonstrated in a fully 3D in vitro reconstructed skin model (T-Skin), which reproduces the dermal and epidermal compartments and allows to study the changes in the extracellular matrix of the dermis and the differentiation of the viable layer (full thickness skin model). TM The model was used to evaluate the effect of

[0138] The above evaluations were performed according to two models, inflammation model A (pretreatment on uninjured tissue) and inflammation model B (pre- and post-treatment on injured tissue), and are reported below.

[0139] II.A. Inflammation Model A for Viable or Inactivated Bacterial Strains II.A.1. Products and Controls Under Analysis - P1: viable LPC-S01 DMS 26760 resuspended in saline, - P2: hyaluronic acid based solution (see I.1.1. Pack); - P3: viable LPC-S01 DMS 26760 resuspended in a hyaluronic acid-based solution, - P1-i.: inactivated LPC-S01 DMS 26760 resuspended in saline, - P2-i.: hyaluronic acid based solutions (see I.1.1. Packs), - P3-i.: inactivated LPC-S01 DMS 26760 resuspended in hyaluronic acid based solution, - Positive Control (PC): tissue treated with 0.9% NaCl saline, scraped and exposed to UV radiation; - Negative control (NC): tissue treated with 0.9% NaCl saline without exposure to UV radiation.

[0140] P1 (viable strains only) and P3 (viable strains + HA) were cultured using lyophilized bacterial strains (CFU 8x10 9 The contents of each capsule were resuspended in 13 ml of saline containing hyaluronic acid.

[0141] P1-i. (inactivated strain only) and P3-i. (inactivated strain + HA) were cultured in lyophilized strain capsules (CFU 8x10 9 ) were resuspended in saline and incubated for 1 h at 85° C. After this period, the bacteria were centrifuged and the pellets were each suspended in 13 ml of hyaluronic acid-based saline (or cream).

[0142] II.A. Methods for Assessing Reduction of UV Damage The reduction of UV damage of the probiotic strain LPC-S01 DSM 26760 (live and viable or inactivated) was evaluated in a "full thickness skin" model as described above. In this study, the effect of the LPC-S01 strain, hyaluronic acid, and a composition containing the LPC-S01 DSM 26760 strain + hyaluronic acid on the morphology of the tissue marked with hematoxylin-eosin and on the activation of inflammasomes in response to UV irradiation was investigated. The strain LPC-S01 DSM 26760, hyaluronic acid, and a composition containing the probiotic strain LPC-S01 DSM 26760 + hyaluronic acid were applied directly to the surface of the 3D skin model and incubated overnight, followed by rinsing using saline to remove excess product (pretreatment step). The tissue was lightly abraded and then exposed to 1 MED (minimal erythema dose) of UV to mimic normal sun exposure. Inflammatory activation was examined 4 and 24 hours after UV exposure. Saline-treated UV-exposed tissues served as positive controls. Saline-treated non-UV-exposed tissues served as negative controls.

[0143] According to methods known to those skilled in the art, the effectiveness of the compositions under analysis in reducing damage caused by ultraviolet light was evaluated using the following: - NFkB immunostaining; - Histomorphological analysis by hematoxylin / eosin (H&E) staining; and - IL-1β quantification method (viable strains only).

[0144] II.A.3. Results of UV Damage Reduction (Inflammation Model A) II.A.3.1.NFkB immunostaining results FIG. 3 summarizes the results of the quantification of NFkB translocation after 4 hours of exposure to UV light (the composition under analysis includes viable strains). Four hours after irradiation, the positive control (PC) showed numerous NFkB translocations, especially in the suprabasal layers of the epidermis. Treatment with LPC-S01 DSM 26760 (P1), strain LPC-S01 DSM 26760 plus hyaluronic acid (P2), and hyaluronic acid (P3) significantly inhibits nuclear translocation of NFkB relative to the positive control. Thus, treatment with probiotics LPC-S01 DSM 26760, LPC-S01 DSM 26760 + hyaluronic acid, and hyaluronic acid demonstrate the ability to prevent inflammatory activation by inhibiting the translocation of NFkB in the nucleus of UV-damaged cells.

[0145] Furthermore, Table 2 shows semi-quantitative data of NFkB nuclear translocation determined for a pretreatment time of 16 hours (long-term) using the compositions under analysis, including viable strains (P3) or inactivated strains (P3-i), as well as parameter evaluation 4 hours after UV irradiation, which is useful for assessing the effect of long-term treatment.

[0146] The biological relevance and reproducibility of the above inflammasome model (UV exposure at 1 MED, minimal erythema dose) was confirmed by increased NFkB translocation in cell nuclei of irradiated samples (positive control) compared to non-irradiated samples (negative control).

[0147] The relative increase (percentage difference) of NFkB translocation in the study with composition P3-i containing inactivated strains (+70.7%, w=0.01) is comparable to that quantified in the study with composition P3 containing viable strains (+83.7, w=0.01).

[0148] Table 2 [Table 3]

[0149] Furthermore, after 24 h, P3 showed a decrease in the cytoplasmic content of NFkB compared to the positive control (data not determined for P3-i).

[0150] II.A.3.2. Histomorphological results by H&E staining Figures 4 and 5 show tissues treated with saline (positive control) (A), probiotic LPC-S01 DSM 26760 (B), hyaluronic acid (C), and LPC-S01 DSM 26760 (viable) + hyaluronic acid (D), respectively, 4 and 24 hours after UV injury (histomorphology by H&E staining).

[0151] As can be seen in both figures, treatment with hyaluronic acid and treatment with the probiotic LPC-S01 DSM 26760 are unable to reduce the UV-induced damage. In particular, signs of UV-induced sunburn can be seen in the basal and spinous layers of the epidermis. Furthermore, the junction of the dermis and epidermis is damaged by UV rays and the epidermis is not fully attached to the dermis, which is a sign of altered skin structure (Figures 4A, 4B, 5A and 5B).

[0152] Treatment with hyaluronic acid + probiotic LPC-S01 DSM 26760 is able to reduce UV-induced damage 4 and 24 hours after the induction of damage. Notably, the structures of both the dermis and epidermis are more compact compared to treatment with hyaluronic acid and probiotic LPC-S01 DSM 26760 individually. Moreover, the structure of the dermis-epidermis junction is better maintained, promoting better attachment of the epidermis to the dermis (Figures 4D and 5D).

[0153] This synergistic effect of the combined administration of hyaluronic acid and the probiotic LPC-S01 DSM 26760 was unexpected, since neither hyaluronic acid nor the probiotic administered alone was able to reduce the "shedding" of the epidermis from the dermis and thus maintain the physiological structure of the skin.

[0154] II.A.3.3. Results of Il-1β quantification IL-1β was quantified at 4 hours for the composition according to the invention P3 with viable strains and hyaluronic acid, against the negative and positive controls (Table 3). Considering that the signal is below the detection limit of the kit (3.91 Pg / mL limit), the results are not considered quantitative data. The results are presented to show the overall trend. Table 3 [Table 4]

[0155] II.A.4. Conclusion T-skin based inflammatory pathways induced by UVA+UVB (1 MED dose) TM An experimental model (full thickness skin) was used to evaluate the efficacy of compositions according to the invention P3 and P3-i comprising the bacterial strain LPC-S01 DMS 26760 (viable or inactivated, respectively) and hyaluronic acid when applied prior to the induction of inflammasome stress (pretreatment).

[0156] Compositions according to the invention P3 (viable strain+HA) and P3-i (inactivated strain+HA) showed good efficacy in reducing NFkB translocation in long-term pretreatment (16 hours).

[0157] Furthermore, composition P3 according to the invention (viable strain+HA) showed a good ability to protect the structure of the dermal-epidermal junction from UV rays in histomorphological studies by H&E staining.

[0158] II.B. Inflammation Model B for Inactivated Bacterial Strains T-skin based inflammatory pathways induced by UVA+UVB (1 MED dose) TM An experimental model (full thickness skin) was used to evaluate the efficacy of the composition P3-i. according to the invention, comprising the inactivated strain LPC-S01 DMS 26760 and hyaluronic acid, applied to damaged tissue before or after the induction of inflammasome stress (pre- or post-treatment with respect to UV irradiation).

[0159] The composition under analysis (see II.B.1) was prepared by two protocols, with the aim of investigating its potential use and efficacy in the T-Skin inflammasome model, by incubating a high concentration of the inactivated bacterial strain under analysis (10 7 or 10 9 cells / tissue) were used to assess:

[0160] BI pretreatment protocol: T skins were abraded by mechanical stress on the epidermal surface and pretreated with the composition under test for 45 minutes or 4 hours, and then subjected to UVA and UVB irradiation (1 MED). After 4 hours of irradiation (post-incubation), tissues were collected and analyzed.

[0161] B.II. Post-treatment protocol: T skins are abraded by mechanical stress at the epidermal surface, subjected to UVA and UVB irradiation (1 MED), treated with the composition under test for 45 minutes or 4 hours, and immediately collected for analysis.

[0162] The aim of the study was to investigate the efficacy of high doses (alone or mixed with HA) of the inactivated assay bacterial strain in modulating the activation and translocation of NFkB in the nucleus.

[0163] II.B.1. Compositions Under Analysis and Controls - P3-i.-10 9 :Inactivated LPC-S0 1DMS 26760(10 9 cells / tissue) were resuspended in a hyaluronic acid-based cream (see I.2.1) representing 30% of the final composition; - P3-i.-107 :Inactivated LPC-S0 1DMS 26760(10 7 cells / tissue) were resuspended in a hyaluronic acid-based cream (see I.2.1) corresponding to 0.03% of the final composition; - Positive control (PC): tissue treated with 0.9% NaCl saline, scraped and exposed to UV light; - Negative control (NC): tissue treated with 0.9% NaCl saline without exposure to UV light.

[0164] P3-i. (inactivated strain + HA) was prepared by resuspending the contents of a freeze-dried bacterial strain capsule (CFU 109) in saline and incubating for 1 h at 85° C. After this period, the bacteria were centrifuged and the pellet was suspended in 13 ml of hyaluronic acid-based cream.

[0165] II.B.2. Research Plan II.B.2.1. Preparation of the composition under analysis The number of cells is 2 × 10 11 The inactivated strains under analysis in lyophilized form at 100 cells / g powder were weighed and resuspended in a suitable solvent as follows: - 2 g in 4 ml of HA-based cream (see I.2.1.), P3-10 9 Get 10 9 bacteria / tissue were applied by applying 15 μL of the suspension. - 0.02 g in 4 ml of HA-based cream (see I.2.1.), P3-10 7 Get 10 7 bacteria / tissue were applied by applying 15 μL of the suspension.

[0166] II.B.2.2. Induction and treatment of inflammasome T-skin II.B.2.2.1. Pretreatment Protocol The experimental design is summarized in Figure 8. On the day of the experiment, tissues were damaged by slight mechanical stress (Algerbrush n strokes = 2) and then treated with T-Skin. TMThe tissue was treated with 15 μL of the assay composition (P3-i.) applied evenly directly to the tissue and incubated for 45 min or 4 h.

[0167] Next, in PBS, a xenon arc lamp and irradiance WG320 [mW / cm 2 ] Oriel 1KW solar simulator equipped with an erythema filter (0.035 mW / cm 2 , according to calibration certificate number 16121 issued by Opto.Cal GmbH) at 1 MED (0.025 J / cm 2 Tissues were irradiated at 1000 x g (equivalent to 1000 x g). After inflammasome induction, tissues were post-incubated under homeostatic conditions for 4 h, fixed in formalin, and then embedded in paraffin (FFPE) for NFκB immunostaining. Tissues were also collected for further RT-qPCR analysis. Carriers were collected and stored at -20°C.

[0168] II.B.2.2.2. Post-treatment protocol The experimental design is summarized in Figure 9: On the day of the experiment, tissues were injured by slight mechanical stress (Algerbrush n strokes = 2) and then irradiated with 1 MED (0.025 J / cm) in PBS. 2 After induction of inflammasomes, the tissues were treated with 15 μL of the composition under analysis and incubated for 45 minutes or 4 hours. Immediately after treatment, the tissues were collected and fixed in formalin for NFκB immunostaining. The tissues were also collected for further RT-qPCR analysis.

[0169] II.B.3.NFkB immunostaining results Table 4 below shows the results of NFkB translocation (expressed as the total number of nuclei detected in three biological replicates) in the negative controls versus the positive controls for each protocol. As reported in Table 4, induction of the inflammasome model was confirmed by an increase in NFkB translocation in cell nuclei of irradiated samples compared to the negative controls.

[0170] However, in this T-skin batch, although translocation was observed at each time point, earlier NFkB activation was observed after irradiation, with the highest induction of NFkB observed at 45 min after irradiation.

[0171] The protocol adopted is based on readings after UV irradiation in a post-treatment model and readings after incubation in a pre-treatment model, when aiming to evaluate the effectiveness of the product on the recovery from acute inflammatory processes. Table 4 [Table 5]

[0172] A) 45 minutes of pretreatment Table 5 shows the semi-quantitative analysis of NFκB nuclear translocation (expressed as the total number of nuclei detected in all biological replicates) for 45 min pretreatment + 4 h post-UV irradiation incubation. Table 5 [Table 6] Composition of the present invention

[0173] B) 4-hour pretreatment Table 6 shows semi-quantitative analysis of NFκB nuclear translocation (expressed as the total number of nuclei detected in all biological replicates) for 4 hours pretreatment + 4 hours post-UV irradiation incubation. Table 6 [Table 7] Composition of the present invention

[0174] Analysis of the results in Tables 5 and 6: - When applied as a pretreatment, composition P3-i., containing inactivated strain LPC-S01 DMS 26760 and hyaluronic acid, is able to reduce NFkB translocation in the nucleus, exhibiting a preventive effect protecting the skin against inflammatory stress induced by UV rays. - Strain concentration is 10 9 In the case of the 45 min pretreatment model, composition P3-i. (inactivated strain + HA) was able to significantly reduce NFkB translocation in the nucleus, indicating a synergistic and / or highly effective effect between the inactivated LPC-S01 DMS 26760 strain and hyaluronic acid. - Composition P3-i. (10 9 ) and P3-i.(10 7 ) pretreatment suggests a dose-response mechanism: fewer NFkB positive nuclei were detected at increasing concentrations of the strain in the composition.

[0175] C) 45 minutes of post-treatment In Table 7, semiquantitative analysis of NFκB nuclear translocation (expressed as the total number of nuclei detected in all biological replicates) is shown for 45 min post-treatment after UV irradiation. Table 7 [Table 8] Composition of the present invention

[0176] D) 4-hour post-treatment In Table 8, semiquantitative analysis of NFκB nuclear translocation (expressed as the total number of nuclei detected in all biological replicates) is shown for 4 h post-treatment after UV irradiation. Table 8 [Table 9] Composition of the present invention

[0177] - Composition P3 (inactivated strain + HA) showed a rapid and effective restoration of basal levels of NFKB, especially in the short term (when the inflammatory response is at its maximum level), suggesting a synergistic / improved effect of the combination of inactivated strain LPC-S01 DMS 26760 + hyaluronic acid in restoring homeostasis in inflamed tissues.

[0178] II.B.4. Conclusion These results confirm that composition P3-i, comprising the combination of inactivated LPC-S01 DMS 26760 + hyaluronic acid, is effective both in homeostatic conditions (see section I.2) and in inflammatory conditions of the skin (e.g. caused by UV irradiation), especially during the acute phase of inflammation, considering that it is particularly effective in the short term of the onset of inflammation.

[0179] Experimental Part (2) Evaluation of the adhesion of Cutibacterium acnes DSM 1897 to a 3D "full thickness skin" model in the presence of a composition according to the invention (strain Lactobacillus paracasei LPC-S01 DSM 26760 and hyaluronic acid) 1. Research Objective The aim of this study was to evaluate the ability of the probiotic strain L. paracasei LPC-S01 DSM 26760, alone and / or in combination with hyaluronic acid (HA), to counteract in vitro adhesion of C. acnes to a “full thickness skin” model.

[0180] Cutibacterium acnes (abbreviated C. acnes, also known as Propionibacterium acnes or P. acnes (Douglas et Gunter, 1946)) is a slow-growing, Gram-positive anaerobic bacterium associated with certain skin diseases such as acne; it can also cause blepharitis and endophthalmitis.

[0181] To evaluate the different possible infection situations, a competition and exclusion model was implemented based on an adaptation of the method described by Coman et al. in 2015.

[0182] 2. Experimental Design The strain C. acnes DSM 1897 was used to simulate infection in a 3D "full thickness skin" model purchased from Phenion (Henkel) with a total of 30 inserts. .

[0183] The study was carried out considering different treatment conditions, which are listed below: 1) evaluate the effective attachment capacity of C. acnes DSM 1897 in no treatment, two exclusion and competition models; 2) prophylactic or concomitant treatment with L. paracasei LPC-S01 DSM 26760 for 24 hours; 3) preventive or concomitant treatment with 0.5% hyaluronic acid (Sigma-Aldrich 41897) for 24 hours; 4) preventive or combined treatment with a homogenous mixture of hyaluronic acid and L. paracasei LPC-S01 DSM 26760 for 24 hours; 5) 24-hour prophylactic or concomitant treatment with benzoyl peroxide (Benzac 10%, positive control).

[0184] A suspension of the strain L. paracasei LPC-S01 DSM 26760 was prepared and 50 μl of the suspension was applied to the surface of the insert.

[0185] A 0.5% hyaluronic acid suspension was prepared and 50 μl of the suspension was contacted with the surface of the insert.

[0186] Additionally, 50 μl of strain L. paracasei LPC-S01 DSM 26760 was mixed with 0.25 mg of hyaluronic acid to obtain a combined probiotic + hyaluronic acid formulation with the same concentration of hyaluronic acid (0.5%) and the same initial loading as those used for testing the individual substances.

[0187] As a positive control, 50 μl of Benzac gel 10% (benzoyl peroxide) was placed in contact with the insert. All five conditions above were tested in duplicate, with 10 inserts in each CO 2 The mixture was incubated at 37°C for 24 hours in the presence of

[0188] 2.a. Performing an Exclusion Test Pretreatment of the inserts with probiotic strains (or hyaluronic acid or a mixture of the two), subsequent infection with the pathogens and exclusion tests provided for the subsequent verification of a possible reduction in the % adhesion of the pathogens to the inserts with regard to ideal conditions for infection (in vitro model of preventive probiotic treatment).

[0189] 2.b. Running competitive tests The simultaneous treatment of the inserts with probiotic strains (or hyaluronic acid or a mixture of the two) and the pathogens and the exclusion test provided for the subsequent verification of a possible reduction in the % adhesion of the pathogens to the inserts with regard to ideal conditions of infection (in vitro model of probiotic treatment during the course of infection).

[0190] 3.Results 3.1 Exclusion Testing FIG. 10 shows the loss of viability of the pathogen C. acnes DMS 1897 expressed in Log10 CFU, while table 9 shows the same situation as the loss of pathogen viability (%) under the various test conditions. Table 9 [Table 10]

[0191] As is evident from the reported results, treatment with Benzac 10%, LPC-S01 DSM 26760, and a combination of LPC-S01 DSM 26760 in the presence of 0.5% hyaluronic acid reduced the viability of C. acnes DSM 1897 by about 1.0-1.4 Log10, which corresponds to a reduction in the viability of the pathogen by about 20%. Treatment with 0.5% hyaluronic acid alone does not appear to reduce the viability of the pathogen at all.

[0192] 3.2. Competitive Exams FIG. 11 and Table 10 show a chart of the survival numbers, expressed as log CFU of the logarithmic reduction of C. acnes DSM 1897 on the inserts, of the percentage reduction obtained in the competition test, of the mean values ​​obtained for the replicates of each test condition. Table 10 [Table 11]

[0193] Based on the presented data, it was confirmed that treatments performed with Benzac 10%, LPC-S01 DSM 26760, and the combination of LPC-S01 DSM 26760 in the presence of 0.5% hyaluronic acid reduce the viability of C. acnes DSM 1897 by 1.0-1.3 Log10 CFU. Similar to the exclusion test, treatment with 0.5% hyaluronic acid alone does not seem to be able to reduce the viability of the pathogen.

[0194] 4. Conclusion All in vitro tests performed demonstrated the effectiveness of Benzac 10% positive control in suppressing infection with C. acnes, reducing the viability of the pathogen population by 15% to 23%.

[0195] Exclusion and competition tests showed that treatment carried out with a combination of LPC-S01 + 0.5% hyaluronic acid (composition according to the invention) reduced infection with C. acnes DSM 1897 by approximately 18-19%.

Claims

1. (I) A bacterial strain belonging to the species Lactobacillus paracasei identified as Lactobacillus paracasei LPC-S01 and deposited at Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (DSMZ) under the accession number DSM 26760; and (II) hyaluronic acid or a salt thereof; A pharmaceutical composition comprising a mixture comprising or consisting of:

2. 10. The pharmaceutical composition of claim 1, further comprising at least one acceptable pharmaceutical or cosmetic or food grade additive and / or excipient.

3. 3. The pharmaceutical composition according to claim 1 or 2, wherein the bacterial strain Lactobacillus paracasei LPC-S01 DSM 26760 is a viable bacterial strain.

4. 3. The pharmaceutical composition according to claim 1 or 2, wherein the bacterial strain Lactobacillus paracasei LPC-S01 DSM 26760 is an inactivated bacterial strain.

5. The pharmaceutical composition according to any one of claims 1 to 4, wherein the pharmaceutical composition is formulated into a cream or pack for topical skin use.

6. The pharmaceutical composition according to any one of claims 1 to 4, wherein the pharmaceutical composition is formulated into a preparation for the formation of a suspension or an extemporaneous suspension for oral use.

7. A pharmaceutical composition according to any one of claims 1 to 6 for use as a medicament.

8. A pharmaceutical composition according to any one of claims 1 to 6 for the preventive and / or curative treatment of inflammations and / or infections of the skin.

9. 9. The pharmaceutical composition of claim 8, wherein the skin inflammation and / or infection is induced by ultraviolet light.

10. 9. The pharmaceutical composition of claim 8, wherein the skin inflammation and / or infection is induced by Cutibacterium acnes or Propionibacterium acnes.

11. UV radiation; and / or Inclement weather conditions for the skin selected from the group consisting of sun, cold and wind; and / or Living conditions harmful to the skin selected from the group consisting of pollution, smoking and drinking alcohol; A pharmaceutical composition according to any one of claims 1 to 6 for the preventive and / or curative treatment of damage caused or induced by.

12. 12. The pharmaceutical composition according to any one of claims 8 to 11, wherein the skin inflammation and / or infection or skin induced damage or associated disease or condition comprises or is selected from the group consisting of acute or chronic skin inflammation or infection, bacterial, viral or fungal infection of the skin, abscess, aposteme, sinusitis, cellulitis, whitlow, furuncle, carbuncle, hidradenitis suppurativa, erysipelas, psoriasis, atopic dermatitis, acne, acute or chronic dermatoses, rosacea, couperosa, erythema, skin redness, burns, sunburn, reactivation of oral herpes, bedsores, ulcers, fissures, fistulas, sores, wounds, bruises, abrasions, ecchymoses, hematomas, excoriations, keratosis, hyperkeratosis, keloids.

13. A pharmaceutical composition according to any one of claims 1 to 5 for maintaining skin homeostasis and / or for use as an anti-aging agent, The pharmaceutical composition, wherein said pharmaceutical composition is used for topical cosmetic skin applications.

14. 14. A pharmaceutical composition according to claim 13 for the treatment of wrinkles, loss of skin elasticity or solar elastosis, dry skin, rough skin, photoaging, redness of the skin, presence of dilated capillaries on the cheeks, nose and / or ears, age spots, abnormal or uneven pigmentation or hyperpigmentation of the skin.

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