624 JOURNAL OF COSMETIC SCIENCE
functions. For studies on fibroblast, we concentrated on ECM components that play a more
structural role, particularly in scar remodelling and tissue integrity. pKTSKS increases
corneal layer thickness and hyaluronic acid synthesis helping to reinforce the skin barrier
and moisturizing functions. We observed that collagen-I, collagen -IV, and fibronectin
production in fibroblasts increased in cells treated with pKTSKS. We hypothesized that
pKTSKS contributes to the improvement of acne scars through dual mechanisms: its
structural role in the dermis, enhancing ECM organization and collagen synthesis, and its
barrier-strengthening role in the epidermis, which enhances hydration and improves tissue
resilience. By targeting both the dermal matrix and epidermal hydration, pKTSKS may act
synergistically to accelerate scar healing and restore skin health.
Associated with C. acnes growth limitation, these data could explain the reduction of redness
and inflammatory blemishes and reduction of roughness observed during clinical tests.
Peptides are known to act safely and efficiently on skin cells and are valuable technologies
for cosmetic industry.17–20,30,31 This pentapeptide modulates skin damage induced by C. acnes
through the control of its quorum to consequently reduce adhesion, biofilm formation and
unpleasant effects on skin (scars, blemishes). In vitro investigations have been confirmed via
two clinical studies that measured skin relief imperfections and facial skin microbiome.
REFERENCES
(1) Byrd AL, Belkaid Y, Segre JA. The human skin microbiome. Nat Rev Microbiol. 2018 16(3):143–155.
doi:10.1038/nrmicro.2017.157
(2) Grice EA, Segre JA. The skin microbiome. Nat Rev Microbiol. 2011 9(4):244–253. doi:10.1038/
nrmicro2537
(3) Kim S, Jazwinski SM. The gut microbiota and healthy aging: a Mini-Review. Gerontology. 2018 64(6):513–
520. doi:10.1159/000490615
(4) Stansbury J. Acne: 4000 consumers speak out. Glob Cosmet Ind Mag. 2020 51–53.
(5) Aubin GG, Portillo ME, Trampuz A, Corvec S. Propionibacterium acnes, an emerging pathogen: from acne
to implant-infections, from phylotype to resistance. Med Mal Infect. 2014 44(6):241–250. doi:10.1016/j.
medmal.2014.02.004
(6) Fitz-Gibbon S, Tomida S, Chiu B-H, et al. Propionibacterium acnes strain populations in the human skin
microbiome associated with acne. J Invest Dermatol. 2013 133(9):2152–2160. doi:10.1038/jid.2013.21
(7) Scholz CFP, Kilian M. The natural history of cutaneous propionibacteria, and reclassification of selected
species within the genus Propionibacterium to the proposed novel genera Acidipropionibacterium
gen nov, Cutibacterium gen nov and Pseudopropionibacterium gen nov. Int J Syst Evol Microbiol.
2016 66(11):4422–4432. doi:10.1099/ijsem.0.001367
(8) Borrel V, Gannesen AV, Barreau M, et al. Adaptation of acneic and non acneic strains of Cutibacterium
acnes to sebum-like environment. Microbiologyopen. 2019 8(9):e00841. doi:10.1002/mbo3.841.
(9) Corvec S. Clinical and biological features of Cutibacterium (formerly Propionibacterium) avidum, an
underrecognized microorganism. Clin Microbiol Rev. 2018 31:1–17.
(10) Huang R, Li M, Gregory RL. Bacterial interactions in dental biofilm. Virulence. 2011 2(5):435–444.
doi:10.4161/viru.2.5.16140
(11) Jahns AC, Lundskog B, Ganceviciene R, et al. An increased incidence of Propionibacterium
acnes biofilms in acne vulgaris: a case-control study. Br J Dermatol. 2012 167(1):50–58.
doi:10.1111/j.1365-2133.2012.10897.x
(12) Jahns AC, Alexeyev OA. Three dimensional distribution of Propionibacterium acnes biofilms in human
skin. Exp Dermatol. 2014 23(9):687–689. doi:10.1111/exd.12482
functions. For studies on fibroblast, we concentrated on ECM components that play a more
structural role, particularly in scar remodelling and tissue integrity. pKTSKS increases
corneal layer thickness and hyaluronic acid synthesis helping to reinforce the skin barrier
and moisturizing functions. We observed that collagen-I, collagen -IV, and fibronectin
production in fibroblasts increased in cells treated with pKTSKS. We hypothesized that
pKTSKS contributes to the improvement of acne scars through dual mechanisms: its
structural role in the dermis, enhancing ECM organization and collagen synthesis, and its
barrier-strengthening role in the epidermis, which enhances hydration and improves tissue
resilience. By targeting both the dermal matrix and epidermal hydration, pKTSKS may act
synergistically to accelerate scar healing and restore skin health.
Associated with C. acnes growth limitation, these data could explain the reduction of redness
and inflammatory blemishes and reduction of roughness observed during clinical tests.
Peptides are known to act safely and efficiently on skin cells and are valuable technologies
for cosmetic industry.17–20,30,31 This pentapeptide modulates skin damage induced by C. acnes
through the control of its quorum to consequently reduce adhesion, biofilm formation and
unpleasant effects on skin (scars, blemishes). In vitro investigations have been confirmed via
two clinical studies that measured skin relief imperfections and facial skin microbiome.
REFERENCES
(1) Byrd AL, Belkaid Y, Segre JA. The human skin microbiome. Nat Rev Microbiol. 2018 16(3):143–155.
doi:10.1038/nrmicro.2017.157
(2) Grice EA, Segre JA. The skin microbiome. Nat Rev Microbiol. 2011 9(4):244–253. doi:10.1038/
nrmicro2537
(3) Kim S, Jazwinski SM. The gut microbiota and healthy aging: a Mini-Review. Gerontology. 2018 64(6):513–
520. doi:10.1159/000490615
(4) Stansbury J. Acne: 4000 consumers speak out. Glob Cosmet Ind Mag. 2020 51–53.
(5) Aubin GG, Portillo ME, Trampuz A, Corvec S. Propionibacterium acnes, an emerging pathogen: from acne
to implant-infections, from phylotype to resistance. Med Mal Infect. 2014 44(6):241–250. doi:10.1016/j.
medmal.2014.02.004
(6) Fitz-Gibbon S, Tomida S, Chiu B-H, et al. Propionibacterium acnes strain populations in the human skin
microbiome associated with acne. J Invest Dermatol. 2013 133(9):2152–2160. doi:10.1038/jid.2013.21
(7) Scholz CFP, Kilian M. The natural history of cutaneous propionibacteria, and reclassification of selected
species within the genus Propionibacterium to the proposed novel genera Acidipropionibacterium
gen nov, Cutibacterium gen nov and Pseudopropionibacterium gen nov. Int J Syst Evol Microbiol.
2016 66(11):4422–4432. doi:10.1099/ijsem.0.001367
(8) Borrel V, Gannesen AV, Barreau M, et al. Adaptation of acneic and non acneic strains of Cutibacterium
acnes to sebum-like environment. Microbiologyopen. 2019 8(9):e00841. doi:10.1002/mbo3.841.
(9) Corvec S. Clinical and biological features of Cutibacterium (formerly Propionibacterium) avidum, an
underrecognized microorganism. Clin Microbiol Rev. 2018 31:1–17.
(10) Huang R, Li M, Gregory RL. Bacterial interactions in dental biofilm. Virulence. 2011 2(5):435–444.
doi:10.4161/viru.2.5.16140
(11) Jahns AC, Lundskog B, Ganceviciene R, et al. An increased incidence of Propionibacterium
acnes biofilms in acne vulgaris: a case-control study. Br J Dermatol. 2012 167(1):50–58.
doi:10.1111/j.1365-2133.2012.10897.x
(12) Jahns AC, Alexeyev OA. Three dimensional distribution of Propionibacterium acnes biofilms in human
skin. Exp Dermatol. 2014 23(9):687–689. doi:10.1111/exd.12482