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Different cutaneous innate immunity profiles in acne patients with and without atrophic scars.

AbstractBACKGROUND:
Acne is a chronic inflammatory disease associated with scar development in many patients.
OBJECTIVES:
To check whether early inflammatory events in the epidermis via keratinocytes influence the development of scars in acne patients.
METHODS:
We investigated several immunological markers involved in epidermal innate immunity in both clinically normal skin and inflammatory early papules in acne patients prone to scars or not.
RESULTS:
In normal skin of acne patients prone to scars vs not prone to scars, TLR-4, IL-2, IL-10, TIMP-2 and JUN were significantly overexpressed and the MMP-9 protein level was decreased. Similar results were obtained in early inflammatory papules (no more than three days), except for TLR-4.
CONCLUSION:
These results suggest for the first time a link between the early events of inflammation with levels of activation of innate immunity in normal epidermis of acne patients and the development of scars. These markers could be a target for drugs in the field of scar prevention.
AuthorsMélanie Saint-Jean, Amir Khammari, Fiona Jasson, Jean-Michel Nguyen, Brigitte Dréno
JournalEuropean journal of dermatology : EJD (Eur J Dermatol) 2016 Jan-Feb Vol. 26 Issue 1 Pg. 68-74 ISSN: 1952-4013 [Electronic] France
PMID27018005 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Biomarkers
  • Cytokines
  • Toll-Like Receptor 2
Topics
  • Acne Vulgaris (immunology, metabolism, pathology)
  • Adolescent
  • Adult
  • Biomarkers (metabolism)
  • Cicatrix (immunology, metabolism, pathology)
  • Cytokines (metabolism)
  • Epidermis (immunology, metabolism)
  • Female
  • Humans
  • Immunity, Innate
  • Keratinocytes (immunology, metabolism)
  • Male
  • Skin (immunology, metabolism, pathology)
  • Toll-Like Receptor 2 (metabolism)
  • Young Adult

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