Dose-Dependent Immunomodulation by Wheat-Grain Moxibustion at Guanyuan (CV4) and Zusanli (ST36) via JAK2/STAT3 Signaling in Cyclophosphamide-Induced Immunosuppressed Rats

Abstract Background Immunosuppression is a critical clinical challenge, and wheat-grain moxibustion (WGM) is a TCM therapy hypothesized to modulate immune function. However, the dose-dependent effects of WGM and its mechanistic link to the JAK2–STAT3 pathway remain understudied. Objectives To investigate the immunopotentiating effects of different dosages of WGM (3, 6, and 9 zhuang) at Guanyuan (CV4) and Zusanli (ST36) on the cyclophosphamide (CTX)-induced immunosuppressed rats, and elucidate its association with the JAK2–STAT3 signaling pathway. Methods Forty-five Sprague–Dawley (SD) rats were randomized into 5 groups: blank control (CON), MG (Model group), and WGM groups (LOW: 3 zhuang, MID: 6 zhuang, and HIGH: 9 zhuang). WGM was applied daily for 7 days. Immune function was assessed via peripheral blood counts (WBC and CD4+/CD8+), organ indices (spleen, thymus), histopathology (HE staining), and molecular markers (JAK2/STAT3 protein/mRNA, cytokines: IgG, IgM, TNF-α, IFN-γ, IL-6, and IL-10). Results Compared to MG, all WGM groups increased WBC counts ( p < 0.05), but the MID (6 zhuang) and HIGH (9 zhuang) groups showed a 1.8-fold and 2.1-fold higher WBC count ( p < 0.01), respectively. Flow cytometry revealed a 2.3-fold increase in CD4+/CD8+ ratio in the HIGH group ( p < 0.01) vs. MG. Histopathology showed restored spleen marginal zones and thymic corticomedullary structure in WGM groups, with the HIGH group exhibiting the least lymphocyte necrosis. Mechanistically, WGM upregulated JAK2/STAT3 phosphorylation (p-JAK2: p < 0.01 in HIGH vs. MG; p-STAT3: p < 0.05 in HIGH vs. MG; p < 0.01) and downstream cytokines (e.g., IFN-γ: in HIGH vs. MG; p < 0.01). Notably, IL-10 (anti-inflammatory) was downregulated in the HIGH group ( p < 0.01), suggesting a shift from immunosuppression to immune activation. Conclusions WGM at Guanyuan and Zusanli ameliorates MG-induced immunosuppression in a dose-dependent manner, with 9 zhuang (HIGH) being the most effective for restoring cellular (CD4+/CD8+) and molecular (JAK2–STAT3) immune function. These findings provide quantitative evidence for optimizing WGM dosage in clinical settings and reveal a novel mechanistic link between TCM therapy and modern immunology. Graphical abstract A graphical abstract that can encompass all the content of this article.

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Journal
Innovations in Acupuncture and Medicine
Published
2025-11-27
DOI
https://doi.org/10.1186/s44424-025-00031-1
Citations
1
Primary Topic
Herbal Medicine Research Studies
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article
Field-Weighted Citation Impact
2.38
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article

Dose-Dependent Immunomodulation by Wheat-Grain Moxibustion at Guanyuan (CV4) and Zusanli (ST36) via JAK2/STAT3 Signaling in Cyclophosphamide-Induced Immunosuppressed Rats

Jing Qin, Tiansheng Zhang, Xiangyue Zhang, Jianguo Li et al.
1 citations
Innovations in Acupuncture and Medicine
Herbal Medicine Research Studies
2.38
article

Dose-Dependent Immunomodulation by Wheat-Grain Moxibustion at Guanyuan (CV4) and Zusanli (ST36) via JAK2/STAT3 Signaling in Cyclophosphamide-Induced Immunosuppressed Rats

Jing Qin, Tiansheng Zhang, Xiangyue Zhang, Jianguo Li, Fang Wang, Tingting Liu, Xiuqing Zhang, Xianjun Meng, Huichao Xu, Muhammad Shahzad Aslam, Xiaoxu Wang
article en
1 citations

Abstract

Abstract Background Immunosuppression is a critical clinical challenge, and wheat-grain moxibustion (WGM) is a TCM therapy hypothesized to modulate immune function. However, the dose-dependent effects of WGM and its mechanistic link to the JAK2–STAT3 pathway remain understudied. Objectives To investigate the immunopotentiating effects of different dosages of WGM (3, 6, and 9 zhuang) at Guanyuan (CV4) and Zusanli (ST36) on the cyclophosphamide (CTX)-induced immunosuppressed rats, and elucidate its association with the JAK2–STAT3 signaling pathway. Methods Forty-five Sprague–Dawley (SD) rats were randomized into 5 groups: blank control (CON), MG (Model group), and WGM groups (LOW: 3 zhuang, MID: 6 zhuang, and HIGH: 9 zhuang). WGM was applied daily for 7 days. Immune function was assessed via peripheral blood counts (WBC and CD4+/CD8+), organ indices (spleen, thymus), histopathology (HE staining), and molecular markers (JAK2/STAT3 protein/mRNA, cytokines: IgG, IgM, TNF-α, IFN-γ, IL-6, and IL-10). Results Compared to MG, all WGM groups increased WBC counts ( p < 0.05), but the MID (6 zhuang) and HIGH (9 zhuang) groups showed a 1.8-fold and 2.1-fold higher WBC count ( p < 0.01), respectively. Flow cytometry revealed a 2.3-fold increase in CD4+/CD8+ ratio in the HIGH group ( p < 0.01) vs. MG. Histopathology showed restored spleen marginal zones and thymic corticomedullary structure in WGM groups, with the HIGH group exhibiting the least lymphocyte necrosis. Mechanistically, WGM upregulated JAK2/STAT3 phosphorylation (p-JAK2: p < 0.01 in HIGH vs. MG; p-STAT3: p < 0.05 in HIGH vs. MG; p < 0.01) and downstream cytokines (e.g., IFN-γ: in HIGH vs. MG; p < 0.01). Notably, IL-10 (anti-inflammatory) was downregulated in the HIGH group ( p < 0.01), suggesting a shift from immunosuppression to immune activation. Conclusions WGM at Guanyuan and Zusanli ameliorates MG-induced immunosuppression in a dose-dependent manner, with 9 zhuang (HIGH) being the most effective for restoring cellular (CD4+/CD8+) and molecular (JAK2–STAT3) immune function. These findings provide quantitative evidence for optimizing WGM dosage in clinical settings and reveal a novel mechanistic link between TCM therapy and modern immunology. Graphical abstract A graphical abstract that can encompass all the content of this article.

Innovations in Acupuncture and MedicineVol. 18(1)
Fujian University of Traditional Chinese Medicine (CN), Xiamen University (CN), First Affiliated Hospital of Xiamen University (CN), Jinzhong University (CN), Xiamen University Malaysia (MY), Shanxi University of Traditional Chinese Medicine (CN), China Association of Acupuncture-Moxibustion (CN)
Openalex Percentile: Top 8%
Herbal Medicine Research Studies
2.38
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