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Published on: November 1, 2024
Propionibacterium acnes promotes Th17 and Th17/Th1 responses in acne patients
Magdalena Kistowska1, Barbara Meier1, Tatiana Proust1
1Department of Dermatology, University Hospital, Zürich, Switzerland.
Abstract:
Propionibacterium acnes is a Gram-positive commensal bacterium thought to be involved in the pathogenesis of acne vulgaris. Although the ability of P. acnes in the initiation of pro-inflammatory responses is well documented, little is known about adaptive immune responses to this bacterium. The observation that infiltrating immune cells consist mainly of CD4(+) T cells in the perifollicular space of early acne lesions suggests that helper T cells may be involved in immune responses caused by the intra-follicular colonization of P. acnes. A recent report showing that P. acnes can induce IL-17 production by T cells suggests that acne might be a T helper type 17 (Th17)-mediated disease. In line with this, we show in this work that, in addition to IL-17A, both Th1 and Th17 effector cytokines, transcription factors, and chemokine receptors are strongly upregulated in acne lesions. Furthermore, we found that, in addition to Th17, P. acnes can promote mixed Th17/Th1 responses by inducing the concomitant secretion of IL-17A and IFN-γ from specific CD4(+) T cells in vitro. Finally, we show that both P. acnes-specific Th17 and Th17/Th1 cells can be found in the peripheral blood of patients suffering from acne and, at lower frequencies, in healthy individuals. We therefore identified P. acnes-responding Th17/Th1 cells as, to our knowledge, a previously unreported CD4(+) subpopulation involved in inflammatory acne.
Insights
Propionibacterium acnes triggers inflammatory responses in acne. Researchers identified a new CD4(+) T cell subpopulation, Th17/Th1, involved in inflammatory acne pathogenesis.
Area of Science:
- Immunology
- Dermatology
- Microbiology
Background:
- Propionibacterium acnes (P. acnes) is a bacterium linked to acne vulgaris pathogenesis.
- While P. acnes' role in initiating inflammation is known, adaptive immune responses are less understood.
- CD4(+) T cells in acne lesions suggest a role for helper T cells in P. acnes-induced inflammation.
Purpose of the Study:
- To investigate adaptive immune responses to P. acnes in acne vulgaris.
- To explore the role of T helper type 17 (Th17) cells in acne.
- To identify specific T cell subpopulations involved in P. acnes-driven inflammation.
Main Methods:
- Analysis of immune cell populations and cytokine profiles in acne lesions.
- In vitro studies of P. acnes-induced T cell responses.
- Detection of P. acnes-specific T cells in patient blood samples.
Main Results:
- Th1 and Th17 effector cytokines, transcription factors, and chemokine receptors are upregulated in acne lesions.
- P. acnes induces mixed Th17/Th1 responses, secreting both IL-17A and IFN-γ from CD4(+) T cells.
- P. acnes-specific Th17 and Th17/Th1 cells are present in acne patients' blood.
Conclusions:
- Acne may involve T helper type 17 (Th17) mediated responses.
- A novel CD4(+) T cell subpopulation, P. acnes-responding Th17/Th1 cells, is identified.
- These Th17/Th1 cells are implicated in the pathogenesis of inflammatory acne.
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