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Protective function of Bu Shen Huo Xue formula on the immunity of B6AF1 mice with experimental autoimmune premature ovarian failure

机译:补肾活血方对实验性自身免疫性卵巢早衰小鼠B6AF1免疫的保护作用。

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摘要

Autoimmune abnormality is one of the main causes of premature ovarian failure (POF). Bu Shen Huo Xue formula (BSHXF), a traditional Chinese medicine formula, has been clinically used for the treatment of patients with POF in China. Regulatory T cells (Tregs) are important in the pathogenesis of autoimmune POF. The aim of the present study was to evaluate the immunoprotective effects of BSHXF on POF and the underlying mechanisms. An experimental autoimmune POF model was induced in B6AF1 mice with zona pellucida 3 (ZP3) fragments. Following modeling, BSHXF (31.53 g/kg/day) was orally administered for 4 weeks. CD4+ T lymphocytes, Tregs, anti-zona pellucida (anti-ZP) antibodies and cytokines were detected using flow cytometry, enzyme-linked immunosorbent assays, reverse transcription-quantitative polymerase chain reaction and immunohistochemistry. The results revealed that BSHXF exhibited an immunoprotective function and reduced inflammatory cell infiltration and damage to the ovary. BSHXF upregulated the percentage of CD4+ CD25+ forkhead box P3+ T cells in the spleen, effectively inhibiting the activation of CD4+ T lymphocytes. The proliferation of Tregs was increased in serum obtained from mice in the BSHXF group in vitro. Anti-ZP antibodies and interleukin-10 and interferon-γ levels were decreased in the serum in the BSHXF-treated group. The present study demonstrated that BSHXF had an immunoprotective effect on POF model mice. Additionally, it indicated that the protective mechanisms of BSHXF may be associated with an increase in Treg cells.
机译:自身免疫异常是卵巢早衰(POF)的主要原因之一。补肾活血配方(BSHXF)是一种中药配方,已在中国临床用于治疗POF患者。调节性T细胞(Tregs)在自身免疫性POF的发病机理中很重要。本研究的目的是评估BSHXF对POF的免疫保护作用及其潜在机制。在具有透明带3(ZP3)片段的B6AF1小鼠中诱导了实验性自身免疫POF模型。建模后,口服给予BSHXF(31.53 g / kg /天),持续4周。使用流式细胞仪,酶联免疫吸附试验,逆转录定量聚合酶链反应和免疫组化检测CD4 + T淋巴细胞,Tregs,抗透明带(ZP)抗体和细胞因子。结果表明,BSHXF具有免疫保护功能,并能减少炎症细胞浸润和对卵巢的损害。 BSHXF上调脾脏CD4 + CD25 + 叉头盒P3 + T细胞的百分比,有效抑制CD4 +的激活 T淋巴细胞。在体外,从BSHXF组的小鼠获得的血清中Treg的增殖增加。 BSHXF治疗组的血清中抗ZP抗体以及白细胞介素10和干扰素-γ水平降低。本研究表明BSHXF对POF模型小鼠具有免疫保护作用。此外,它表明BSHXF的保护机制可能与Treg细胞的增加有关。

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