欧洲食物安全局利用 NAMs 探讨全氟辛烷磺酸免疫毒性的项目

Emanuela Corsini, Martina Iulini, Valentina Galbiati, Ambra Maddalon, Francesco Pappalardo, Giulia Russo, Ron L.A.P. Hoogenboom, Karsten Beekmann, Aafke W.F. Janssen, Jochem Louisse, Styliani Fragki, Alicia Paini
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引用次数: 0

摘要

全氟辛烷磺酸(PFAS)是一类广泛应用于工业领域的合成化学品,人类和生态系统都会接触到它。流行病学研究表明,全氟辛烷磺酸可导致免疫抑制、感染风险增加和疫苗接种反应下降,但其潜在的作用机制仍然难以捉摸。本项目旨在利用新方法(NAMs)填补 2020 年欧洲食品安全局意见书中确定的一些数据缺口。特别是,我们旨在获得在流行病学研究中观察到的免疫抑制效应(即降低疫苗接种效果和可能增加对传染病的易感性)的作用模式方面的信息,并解决除全氟辛烷磺酸和全氟己酸(PFNA 和 PFHxS)以外的全氟辛烷磺酸的免疫毒性问题,包括评估可能的共同作用模式,并深入了解受测全氟辛烷磺酸的相对效力。为了实现这些目标,我们制定了一项综合测试策略 (ITS),其中包括体外和硅学方法。全氟辛烷磺酸的影响是通过基于目标免疫人体细胞的体外模型进行研究的,该模型适用于评估流行病学研究中观察到的相关免疫毒性参数(即抗体生成减少)。研究结果完全支持人类流行病学研究的证据。此外,还利用数学转归和分布模型来确定体外细胞系统中全氟辛烷磺酸的标称浓度,并利用生理学动力学(PBK)模型进行从体外到体内的定量推断。使用 "通用免疫系统模拟器 "完成 ITS,并调查易感人群对疫苗接种反应的降低情况。通过提供机理信息,使用这些选定的 NAM 可以为监管风险评估提供支持,并研究其他全氟辛烷磺酸的免疫毒性潜力。免疫毒理学家、分子生物学家、风险评估员和计算专家参与了该联盟,再加上欧洲食品安全局的参与,确保了该项目的成功实施,并交付了基于 NAMs 的战略,从而能够生成有关全氟辛烷磺酸免疫毒性的机理信息并支持风险评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EFSA Project on the use of NAMs to explore the immunotoxicity of PFAS

Perfluorinated substances (PFAS) are a class of synthetic chemicals widely used in industry, to which people and ecosystems are exposed. Epidemiological studies have shown that PFAS can cause immunosuppression, increased risk of infections and decreased response to vaccination, with the underlying mechanism(s) of action still remaining elusive. The aim of this project was to fill some of the data gaps identified in the 2020 EFSA Opinion, using new approach methodologies (NAMs). In particular, we aimed to get information on the mode of action for the immunosuppression effects observed in epidemiological studies (i.e., reduction in the vaccination efficacy and possible increase in the susceptibility to infectious disease), and to address the immunotoxicity of PFAS other than PFOS and PFOA (PFNA and PFHxS), including the assessment of a possible common mode of action and to provide insight into the relative potencies of the tested PFAS. To reach these goals, an integrated testing strategy (ITS) consisting of in vitro and in silico methods was developed. The effects of PFAS were investigated using target immune human cell-based in vitro models, suitable to assess the relevant immunotoxic parameters observed in epidemiological studies (i.e. decreased antibody production). Results obtained fully support the evidence from human epidemiological studies. Furthermore, mathematical fate and distribution models were used to identify nominal concentration of PFAS in the in vitro cell system and physiologically based kinetic (PBK) models were used to perform quantitative in vitro to in vivo extrapolation. The ‘Universal Immune System Simulator’ was used to complete the ITS and investigate the reduced response to vaccination also on vulnerable populations. The use of these selected NAMs may provide a tool to support, by providing mechanistic information, regulatory risk assessment and to study the immunotoxic potential of other PFAS. The participation of immunotoxicologists, molecular biologists, risk assessors, and computational experts within the Consortium, together with EFSA's engagement, ensured the successful performance of this project and delivery of a NAMs-based strategy that allows generating mechanistic information on PFAS immunotoxicity and support risk assessment.

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