Timothy M Pierpont, Jessica Elmore, Amie Redko, Orchi Anannya, Brian Imbiakha, Katelyn O'Hare, Alanis Villanueva, Sasha Anronikov, Narda Bondah, Sue Chang, Julie Sahler, Avery August
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In this study, we analyze immune cell numbers in mice following 28-d repeated oral exposure to potassium PFHxS at 12, 120, 1,200, and 12,000 ng/kg/d, with resulting serum levels ranging up to ∼1,600 ng/ml, approximating ranges found in the general population and at higher levels in PFAS workers. The immunosuppressant cyclophosphamide was analyzed as a positive control. B cells, T cells, and granulocytes from the bone marrow, liver, spleen, lymph nodes, and thymus were evaluated. We found that at these exposures, there was no effect of PFHxS on major T or B cell populations, macrophages, dendritic cells, basophils, mast cells, eosinophils, neutrophils, or circulating Ab isotypes. By contrast, mice exposed to cyclophosphamide exhibited depletion of several granulocyte and T and B cell populations in the thymus, bone marrow, and spleen, as well as reductions in IgG1, IgG2b, IgG2c, IgG3, IgE, and IgM. 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引用次数: 0
摘要
全氟己烷磺酸(PFHxS)是全氟烷基和多氟烷基(PFAS)超家族分子中的一员,其特点是碳链含氟,并广泛应用于工业领域。全氟己烷磺酸和全氟辛烷磺酸能够在环境和人体中积累,血清消除半衰期约为数年。最近,一些全氟辛烷磺酸化合物还被认为是潜在的免疫抑制剂。在这项研究中,我们分析了小鼠在重复口服 12、120、1,200 和 12,000 纳克/千克/天的全氟己烷磺酸钾 28 天后的免疫细胞数量,结果发现小鼠血清中的全氟己烷磺酸钾含量高达 1,600 纳克/毫升,接近普通人群中的含量范围,而全氟辛烷磺酸工人的含量则更高。免疫抑制剂环磷酰胺作为阳性对照进行了分析。对骨髓、肝脏、脾脏、淋巴结和胸腺中的 B 细胞、T 细胞和粒细胞进行了评估。我们发现,在这些暴露条件下,PFHxS 对主要 T 细胞或 B 细胞群、巨噬细胞、树突状细胞、嗜碱性粒细胞、肥大细胞、嗜酸性粒细胞、中性粒细胞或循环抗体异型均无影响。相比之下,暴露于环磷酰胺的小鼠胸腺、骨髓和脾脏中的几种粒细胞、T 细胞和 B 细胞群会出现衰竭,IgG1、IgG2b、IgG2c、IgG3、IgE 和 IgM 也会减少。这些数据表明,连续 28 天接触 12,000 纳克/千克 PFHxS 不会影响天真小鼠的免疫细胞数量,这为评估接触这种化合物的风险和对健康的影响提供了宝贵的信息。
Effects of Perfluorohexane Sulfonate Exposure on Immune Cell Populations in Naive Mice.
Perfluorohexane sulfonate (PFHxS) is a member of the per- and polyfluoroalkyls (PFAS) superfamily of molecules, characterized by their fluorinated carbon chains and use in a wide range of industrial applications. PFHxS and perfluorooctane sulfonate are able to accumulate in the environment and in humans with the approximated serum elimination half-life in the range of several years. More recently, some PFAS compounds have also been suggested as potential immunosuppressants. In this study, we analyze immune cell numbers in mice following 28-d repeated oral exposure to potassium PFHxS at 12, 120, 1,200, and 12,000 ng/kg/d, with resulting serum levels ranging up to ∼1,600 ng/ml, approximating ranges found in the general population and at higher levels in PFAS workers. The immunosuppressant cyclophosphamide was analyzed as a positive control. B cells, T cells, and granulocytes from the bone marrow, liver, spleen, lymph nodes, and thymus were evaluated. We found that at these exposures, there was no effect of PFHxS on major T or B cell populations, macrophages, dendritic cells, basophils, mast cells, eosinophils, neutrophils, or circulating Ab isotypes. By contrast, mice exposed to cyclophosphamide exhibited depletion of several granulocyte and T and B cell populations in the thymus, bone marrow, and spleen, as well as reductions in IgG1, IgG2b, IgG2c, IgG3, IgE, and IgM. These data indicate that exposures of up to 12,000 ng/kg of PFHxS for 28 d do not affect immune cell numbers in naive mice, which provides valuable information for assessing the risks and health influences of exposures to this compound.