Baicalin attenuates PD-1/PD-L1 axis-induced immunosuppression in piglets challenged with Glaesserella parasuis by inhibiting the PI3K/Akt/mTOR and RAS/MEK/ERK signalling pathways

黄芩苷 左旋咪唑 免疫抑制 CD8型 CD3型 生物 PI3K/AKT/mTOR通路 免疫学 免疫系统 分子生物学 化学 信号转导 生物化学 高效液相色谱法 色谱法
作者
Shulin Fu,Jingyang Li,Jiarui You,Siyu Liu,Qiaoli Dong,Yunjian Fu,Ronghui Luo,Yamin Sun,Xinyue Tian,Wei Liu,Jingyi Zhang,Yu‐Qiang Ding,Yitian Zhang,W. Wang,Ling Guo,Yinsheng Qiu
出处
期刊:Veterinary Research [BioMed Central]
卷期号:55 (1) 被引量:2
标识
DOI:10.1186/s13567-024-01355-1
摘要

Abstract Infection of piglets with Glaesserella parasuis ( G. parasuis ) induces host immunosuppression. However, the mechanism underlying the immunosuppression of piglets remains unclear. Activation of the PD-1/PD-L1 axis has been shown to trigger host immunosuppression. Baicalin possesses anti-inflammatory and immunomodulatory functions. However, whether baicalin inhibits PD-1/PD-L1 activation and thus alleviates host immunosuppression has not been investigated. In this study, the effect of baicalin on the attenuation of piglet immunosuppression induced by G. parasuis was evaluated. Seventy piglets were randomly divided into the control group, infection group, levamisole group, BMS-1 group, 25 mg/kg baicalin group, 50 mg/kg baicalin group and 100 mg/kg baicalin group. Following pretreatment with levamisole, BMS-1 or baicalin, the piglets were challenged with 1 × 10 8 CFU of G. parasuis . Our results showed that baicalin, levamisole and BMS-1 modified routine blood indicators and biochemical parameters; downregulated IL-1β, IL-10, IL-18, TNF-α and IFN-γ mRNA expression; and upregulated IL-2 and IL-8 mRNA expression in blood. Baicalin, levamisole and BMS-1 increased the proportions of CD3 + T cells, CD3 + CD4 + T cells, CD3 + CD8 + T cells and CD3 – CD21 + B cells in the splenocyte population, increased the proportions of CD3 + T cells, CD3 + CD4 + T cells and CD3 + CD8 + T cells in the blood, and inhibited PD-1/PD-L1 and TIM-3 activation. Baicalin, levamisole and BMS-1 reduced p-PI3K, p-Akt, and p-mTOR expression, the p-MEK1/2/MEK1/2 and p-ERK1/2/ERK1/2 ratios and increased RAS expression. Baicalin, levamisole and BMS-1 provided substantial protection against G. parasuis challenge and relieved tissue histopathological damage. Our findings might provide new strategies for controlling G. parasuis infection and other immunosuppressive diseases.
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