Studies of the human skin microbiome suggest that Propionibacterium acnes strains may contribute differently to skin health and disease. However, the immune phenotype and functions of T helper type 17 (Th17) cells induced by healthy (P) versus acne (P) skin-associated P. acnes strains are currently unknown. We stimulated peripheral blood mononuclear cells from healthy donors and observed that Pstrains induce higher IL-17 levels than Pstrains. We next generated Pand Pstrain-specific Th17 clones and show that P. acnes strains induce Th17 cells of varied phenotype and function that are stable in the presence of IL-2 and IL-23. Although P- and P-specific clones expressed similar levels of LL-37 and DEFB4, only P-specific clones secreted molecules sufficient to kill P. acnes. Furthermore, electron microscopic studies showed that supernatants derived from activated Pand not P-specific clones exhibited robust bactericidal activity against P. acnes, and complete breaches in the bacterial cell envelope were observed. This antimicrobial activity was independent of IL-26, because both natural IL-26 released by Th17 clones and rhIL-26 lacked antimicrobial potency against P. acnes. Overall, our data suggest that P. acnes strains may differentially modulate the CD4T-cell responses, leading to the generation of Th17 cells that may contribute to either homeostasis or acne pathogenesis.
Authors
Agak, George W; Kao, Stephanie; Ouyang, Kelsey; Qin, Min; Moon, David; Butt, Ahsan; Kim, Jenny