Department of Pharmacy, the First Affiliated Hospital of Nanchang University, 330006, Nanchang, Jiangxi, People's Republic of China.
Department of Otorhinolaryngology, Head & Neck Surgery, the First Affiliated Hospital of Nanchang University, 330006, Nanchang, Jiangxi, People's Republic of China.
BMC Endocr Disord. 2022 Jul 16;22(1):179. doi: 10.1186/s12902-022-01093-5.
While contributions of dyslipidemia to autoimmune diseases have been described, its impact on thyroid autoimmunity (TA) is less clear. Programmed cell death 1(PD-1)/PD-ligand 1 (PD-L1) immune checkpoint is crucial in preventing autoimmune attack while its blockade exacerbates TA. We thus unveiled the effect of high-fat diet (HFD) on TA, focusing on the contribution of PD-1/PD-L1.
Female Sprague Dawley (SD) rats were randomly fed with a regular diet or HFD (60% calories from fat) for 24 weeks. Then, thyroid ultrasonography was performed and samples were collected for lipid and thyroid-related parameter measure.
HFD rats exhibited hyperlipemia and abnormal biosynthesis of the unsaturated fatty acid in serum detected by lipidomics. These rats displayed a relatively lower echogenicity and increased inflammatory infiltration in thyroid accompanied by rising serum thyroid autoantibody levels and hypothyroidism, mimicking human Hashimoto's thyroiditis. These alterations were concurrent with decreased mRNA and immunostaining of intrathyroidal PD-1 and also serum PD-1 levels but not the PD-L1 expression, suggesting a role of a PD-1 pathway. Meanwhile, the infiltration of B and T cell, a key cellular event inhibited by the PD-1 signals, was enhanced in the thyroid of HFD rats, along with thyroid fibrosis and apoptosis.
Our data suggest that HFD triggers TA through a mechanism possibly involving downregulation of PD-1-related immunosuppression, providing a novel insight into the link between dyslipidemia and autoimmune toxicities.
虽然血脂异常对自身免疫性疾病的贡献已有描述,但它对甲状腺自身免疫(TA)的影响尚不清楚。程序性细胞死亡 1(PD-1)/PD-配体 1(PD-L1)免疫检查点在防止自身免疫攻击中至关重要,而其阻断则会加剧 TA。因此,我们揭示了高脂肪饮食(HFD)对 TA 的影响,重点关注 PD-1/PD-L1 的作用。
雌性 Sprague Dawley(SD)大鼠随机分为正常饮食组或 HFD 组(60%的热量来自脂肪)喂养 24 周。然后进行甲状腺超声检查,并采集样本以测量血脂和甲状腺相关参数。
HFD 大鼠表现出高脂血症和脂质组学检测到的血清中不饱和脂肪酸异常合成。这些大鼠的甲状腺回声相对较低,炎症浸润增加,同时伴有血清甲状腺自身抗体水平升高和甲状腺功能减退,模拟人类桥本甲状腺炎。这些改变与甲状腺内 PD-1 的 mRNA 和免疫染色减少以及血清 PD-1 水平降低有关,但 PD-L1 表达不变,提示 PD-1 途径的作用。同时,HFD 大鼠甲状腺中 B 和 T 细胞浸润增强,这是 PD-1 信号抑制的关键细胞事件,同时伴有甲状腺纤维化和凋亡。
我们的数据表明,HFD 通过可能涉及下调 PD-1 相关免疫抑制的机制引发 TA,为血脂异常与自身免疫毒性之间的联系提供了新的见解。