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Immunomodulatory Effects of Yu-Ping-Feng Formula on Primary Sjögren's Syndrome: Interrogating the T Cell Response.
Yu, Sulan; Zhou, Xinyao; Liu, Ruihua; Xu, Xiaoyu; Ma, Danbao; Feng, Yun; Lin, Xiang.
Afiliação
  • Yu S; School of Chinese Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hon Kong SAR 999077, China.
  • Zhou X; 2Department of Rheumatology, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijng 100053, China.
  • Liu R; 2Department of Rheumatology, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijng 100053, China.
  • Xu X; School of Chinese Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hon Kong SAR 999077, China.
  • Ma D; School of Chinese Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hon Kong SAR 999077, China.
  • Feng Y; Department of Ophthalmology, Peking University Third Hospital, Beijing 100191, China.
  • Lin X; School of Chinese Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hon Kong SAR 999077, China.
J Leukoc Biol ; 2024 Jul 02.
Article em En | MEDLINE | ID: mdl-38953166
ABSTRACT
Ethnopharmacological treatments have shown beneficial effects in the clinical practice of autoimmune disorders. However, the underlying mechanism of immunomodulatory effects remains challenging, given the complicate composition of herbal medicines. Here, we developed an immunological approach to interrogate the T helper cell response. Through data mining we hypothesized that Chinese medicine formula, Yu-Ping-Feng (YPF) might be a promising candidate for treating primary Sjögren's syndrome (pSS), a common autoimmune disease manifested by exocrine gland dysfunction. We took advantage of a mouse model of experimental Sjögren's syndrome (ESS) that we previously established for YPF formula treatment. YPF therapy ameliorated the ESS pathology in mice with active disease, showing improved salivary function and decreased serum levels of autoantibodies. Phenotypic analysis suggested that both effector T and B cells were significantly suppressed. Using co-culture assay and adoptive transfer models, we demonstrated that YPF formula directly restrained effector/memory T cell expansion and differentiation into Th17 and T follicular helper (Tfh) cells, the key subsets in ESS pathogenesis. Importantly, we recruited 20 pSS patients and conducted a pilot study of 8-week therapy of YPF formula. YPF treatment effectively improved fatigue symptoms, exocrine gland functions and reduced serum IgG/IgA levels, while effector T and B cell subsets were significantly decreased. There was a trend of reduction on disease activity, but not statistically significant. Together, our findings suggested a novel approach to assess the immunomodulatory effects of YPF formula, which may be favorable for patients with autoimmune disorders.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Leukoc Biol Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Leukoc Biol Ano de publicação: 2024 Tipo de documento: Article