Acne is the most common inflammatory dermatosis, affecting up to 85% of the 11-30 years old world population. [1] This disease is subdivided according to severity graduation, from minor to severe acne, and affects different body localizations from face to back. [2] The mechanisms leading to severe acne, representing up to 20% of acne patients, are still poorly understood, although Cutibacterium acnes (C. acnes) appears as a key player of acne physiopathology.Recently, an increasing interest was observed related to skin microbiota's impact on innate immunity, and subsequently, on inflammatory dermatoses physiopathology. [3,4] Two major studies previously decrypted skin microbiota in acne context; however, this topic remains poorly documented-especially on the back-and the sampling methodologies used were quite controversial. [5][6][7] Indeed, Barnard et al and Fitz-Gibbon et al both described skin microbiome in acne and healthy context, using strip from nose of patients. [8,9] These studies both showed that no clear difference was observed in C. acnes abundance between healthy and acne individuals, whereas recent evidences highlighted a loss of C. acnes subgroups diversity in severe acne context. [10] On the other hand, studying skin bacterial populations using either 16S metataxonomic method or shotgun, to reveal the skin microbial composition, have never been described before in severe back acne context. The present study aims to investigate skin microbiota in patients with severe acne of the back vs healthy controls, sampling two major localizations of acne lesions: the back and the face.
| MATERIAL AND ME THODS
| Recruitment of healthy volunteers and patientsIn the present clinical study, 24 patients with severe acne of the back and 12 healthy volunteers were enrolled. Regarding the skin type, all Abstract Acne is the most common inflammatory skin disease, affecting up to 85% of the 11-30 years old world population. Skin microbiota appears as a key player involved in several skin dermatoses physiopathology. Here, we show that inflammatory skin is associated with changes in the skin microbiota composition on the back of severe acne patients but also on the face of patients where acne was scored as mild to moderate, comparing with healthy controls. Changes were observed particularly on skin commensals Propionibacteriaceae, Staphylococcaceae and Enterococcaceae families, suggesting the importance of the balance between skin commensals to maintain skin homeostasis and control skin inflammatory process.
K E Y W O R D Sacne, inflammatory skin diseases, innate immunity, microbiology, microbiome