A four-herb topical formula attenuates psoriasis-like skin inflammation by suppressing IL-17-mediated inflammation and pathogenic γδT17 cell infiltration
11 affiliations
- 1Department of Chinese Medicine, Taichung Tzu Chi Hospital
- 2Graduate Institute of Integrated Medicine, College of Chinese Medicine, China Medical University
- 3School of Chinese Medicine, College of Chinese Medicine, China Medical University
- 4Research Center for Traditional Chinese Medicine, Department of Medical Research, China Medical University Hospital
- 5Chinese Medicine Research Center, China Medical University
- 6Department of Chinese Medicine, China Medical University Hospital
- 7Office of Research and Development, Asia University
- 8Department of Clinical Research Center of Integrated Medicine, Taichung Tzu Chi Hospital
- 9Department of Cosmeceutics, China Medical University
- 10Drug Development Research Unit, Research Center for Traditional Chinese Medicine, China Medical University Hospital
- 11Department of Chinese Pharmaceutical Sciences and Chinese Medicine Resources, College of Chinese Medicine, China Medical University
Abstract
Background: Psoriasis is a chronic immune-mediated inflammatory skin disease driven by dysregulation of IL-17-mediated immune responses. Current topical therapies, including corticosteroids, are limited by long-term side effects, creating demand for safer alternatives. DH-YH is a novel four-herb Traditional Chinese Medicine (TCM) formula derived from Duhuo Jisheng Tang, comprising Angelica pubescens , Gentiana macrophylla , Taxillus chinensis , and Paeonia lactiflora . Based on an initial clinical observation of improvement following topical DH-YH treatment in a patient with psoriasis, this study investigated its immunomodulatory effects in psoriasis-related models.
Methods: The anti-inflammatory effects of DH-YH were assessed in vitro using IL-17A-stimulated human keratinocytes (HaCaT cells) and LPS-activated bone marrow-derived dendritic cells (BMDCs) and RAW264.7 macrophages. The effects on T-cell polarization were evaluated in murine splenic CD4 ⁺ T cells differentiated toward Th1, Th2, and Th17 lineages. In vivo , an imiquimod (IMQ)-induced psoriasis-like mouse model (BALB/c, n = 5/group) was used to evaluate topical DH-YH ointment. Skin histopathology (H&E staining) and multi-organ flow cytometric analysis (skin, spleen, and lymph nodes) were performed to assess epidermal thickness, inflammatory infiltration, and immune cell subset frequencies.
Results: Topical DH-YH ointment markedly improved psoriatic lesions in a clinical case without hepatorenal toxicity. In vitro , DH-YH dose-dependently suppressed IL-8 secretion in IL-17A-stimulated HaCaT cells and inhibited TNF-α and IL-6 production in LPS-activated BMDCs. DH-YH also significantly reduced Th17 and Th2 cell differentiation without affecting cell viability. In the IMQ-induced mouse model, topical DH-YH significantly reduced epidermal thickness and dermal inflammatory cell infiltration. Flow cytometric analysis revealed that DH-YH specifically decreased the proportions of CD45 ⁺ , CD3 ⁺ , γδT, and γδT17 cells in lesional skin.
Conclusion: DH-YH attenuates psoriasis-related inflammatory responses across multiple cellular and immune components, including keratinocyte inflammatory responses, BMDC cytokine production, T helper cell differentiation, and γδT17 cell accumulation.
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BibTeX
@article{cheng2026fourherb,
title = {{A four-herb topical formula attenuates psoriasis-like skin inflammation by suppressing IL-17-mediated inflammation and pathogenic γδT17 cell infiltration}},
author = {Chun-Yao Cheng and Ping Chen and Dao-Syuan Wu and Hung-Rong Yen and Mei-Yun Chu and Shu-Cheng Tseng and Chia-Lin Lee and Chuan-Teng Liu and Ying-Chyi Song},
journal = {Frontiers in Pharmacology},
year = {2026},
month = oct,
doi = {10.3389/fphar.2026.1957818},
url = {https://www.frontiersin.org/articles/10.3389/fphar.2026.1957818/full},
note = {CC BY 4.0},
}
RIS
TY - JOUR
TI - A four-herb topical formula attenuates psoriasis-like skin inflammation by suppressing IL-17-mediated inflammation and pathogenic γδT17 cell infiltration
AU - Chun-Yao Cheng
AU - Ping Chen
AU - Dao-Syuan Wu
AU - Hung-Rong Yen
AU - Mei-Yun Chu
AU - Shu-Cheng Tseng
AU - Chia-Lin Lee
AU - Chuan-Teng Liu
AU - Ying-Chyi Song
PY - 2026
DA - 2026/10/28
JO - Frontiers in Pharmacology
DO - 10.3389/fphar.2026.1957818
UR - https://www.frontiersin.org/articles/10.3389/fphar.2026.1957818/full
AB - Background: Psoriasis is a chronic immune-mediated inflammatory skin disease driven by dysregulation of IL-17-mediated immune responses. Current topical therapies, including corticosteroids, are limited by long-term side effects, creating demand for safer alternatives. DH-YH is a novel four-herb Traditional Chinese Medicine (TCM) formula derived from Duhuo Jisheng Tang, comprising Angelica pubescens , Gentiana macrophylla , Taxillus chinensis , and Paeonia lactiflora . Based on an initial clinical observation of improvement following topical DH-YH treatment in a patient with psoriasis, this study investigated its immunomodulatory effects in psoriasis-related models. Methods: The anti-inflammatory effects of DH-YH were assessed in vitro using IL-17A-stimulated human keratinocytes (HaCaT cells) and LPS-activated bone marrow-derived dendritic cells (BMDCs) and RAW264.7 macrophages. The effects on T-cell polarization were evaluated in murine splenic CD4 ⁺ T cells differentiated toward Th1, Th2, and Th17 lineages. In vivo , an imiquimod (IMQ)-induced psoriasis-like mouse model (BALB/c, n = 5/group) was used to evaluate topical DH-YH ointment. Skin histopathology (H&E staining) and multi-organ flow cytometric analysis (skin, spleen, and lymph nodes) were performed to assess epidermal thickness, inflammatory infiltration, and immune cell subset frequencies. Results: Topical DH-YH ointment markedly improved psoriatic lesions in a clinical case without hepatorenal toxicity. In vitro , DH-YH dose-dependently suppressed IL-8 secretion in IL-17A-stimulated HaCaT cells and inhibited TNF-α and IL-6 production in LPS-activated BMDCs. DH-YH also significantly reduced Th17 and Th2 cell differentiation without affecting cell viability. In the IMQ-induced mouse model, topical DH-YH significantly reduced epidermal thickness and dermal inflammatory cell infiltration. Flow cytometric analysis revealed that DH-YH specifically decreased the proportions of CD45 ⁺ , CD3 ⁺ , γδT, and γδT17 cells in lesional skin. Conclusion: DH-YH attenuates psoriasis-related inflammatory responses across multiple cellular and immune components, including keratinocyte inflammatory responses, BMDC cytokine production, T helper cell differentiation, and γδT17 cell accumulation.
SN - 1663-9812
ER -