Evaluating the conduct and reporting of the T-cell dependent antibody response in the Extended One-Generation Reproductive Toxicity study provided under the EU REACH regulation.

IF 5.7 2区 医学 Q1 TOXICOLOGY Critical Reviews in Toxicology Pub Date : 2024-08-01 Epub Date: 2024-07-23 DOI:10.1080/10408444.2024.2377203
Rob J Vandebriel, Betty Hakkert, Jeroen L A Pennings, Laura H Rossi, Ingo Bichlmaier, Wieneke Bil
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Abstract

The European Union (EU) Chemicals Strategy for Sustainability regards chemicals that affect the immune system among the most harmful ones. The Extended One-Generation Reproductive Toxicity study (EOGRTS; Organisation for Economic Co-Operation and Development (OECD) Test Guideline (TG) 443), addresses, among others, potential effects of chemicals on development. In specific cases, the EOGRTS is performed with addition of a so-called cohort 3, that addresses potential effects on the developing immune system, by means of a central assay measuring the T-cell dependent antibody response (TDAR). This assay is based on an interplay of antigen presentation, T-cell help and antibody production by B-cells, and together comprises a functional immune response. In the context of the EOGRTS review project of the European Chemicals Agency (ECHA), we evaluated 15 available TDARs for compliance with conduct and reporting requirements. Collectively, the majority of the TDAR studies were considered to be adequately conducted. We however observed: (i) the protocols differed by the antigen used (sheep red blood cells (SRBC) or KLH), the route of administration (intravenous, intraperitoneal, or subcutaneous), prime or prime/boost immunizations, and whether IgG was measured. (ii) There was major variation in the effects of the positive control for immunosuppression, cyclophosphamide. (iii) Proficiency was not always shown. (iv) Statistical analysis was not always done or reported. (v) Results of effects on lymphocyte populations or other immunotoxicity observations obtained in cohort 1 (or 2) of the EOGRTS were not always discussed together with results of the TDAR. Taken together, next to an improved quality of reporting, this may suggest a need to better define the conduct of the TDAR in OECD TG 443 and OECD Guidance Document (GD) 151, at least for certain aspects.

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评估欧盟 REACH 法规规定的扩展一代生殖毒性研究中 T 细胞依赖性抗体反应的实施和报告情况。
欧洲联盟(欧盟)化学品可持续发展战略将影响免疫系统的化学品视为最有害的化学品。扩展的一代生殖毒性研究(EOGRTS;经济合作与发展组织(OECD)测试指南(TG)443)主要针对化学品对发育的潜在影响。在特定情况下,在进行 EOGRTS 试验时,会增加所谓的队列 3,通过测量 T 细胞依赖性抗体反应 (TDAR) 的中心检测法来解决对发育中的免疫系统的潜在影响。该检测基于抗原呈递、T 细胞帮助和 B 细胞产生抗体的相互作用,共同构成了功能性免疫反应。在欧洲化学品管理局 (ECHA) 的 EOGRTS 审查项目中,我们对 15 种可用的 TDAR 进行了评估,以确定其是否符合行为和报告要求。总体而言,大多数 TDAR 研究都被认为是充分进行的。不过,我们注意到(i) 使用的抗原(绵羊红细胞 (SRBC) 或 KLH)、给药途径(静脉注射、腹腔注射或皮下注射)、初次免疫或初次/加强免疫,以及是否测量 IgG,这些方案各不相同。(ii) 免疫抑制阳性对照环磷酰胺的效果差异很大。(iii) 并非总能显示出熟练程度。(iv) 并非总是进行或报告统计分析。(v) 在 EOGRTS 第 1 组(或第 2 组)中获得的对淋巴细胞群的影响结果或其他 免疫毒性观察结果并不总是与 TDAR 的结果一起讨论。总之,除了提高报告质量之外,这可能表明需要在 OECD TG 443 和 OECD 指导文件 (GD) 151 中更好地界定 TDAR 的进行,至少在某些方面。
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来源期刊
CiteScore
9.50
自引率
1.70%
发文量
29
期刊介绍: Critical Reviews in Toxicology provides up-to-date, objective analyses of topics related to the mechanisms of action, responses, and assessment of health risks due to toxicant exposure. The journal publishes critical, comprehensive reviews of research findings in toxicology and the application of toxicological information in assessing human health hazards and risks. Toxicants of concern include commodity and specialty chemicals such as formaldehyde, acrylonitrile, and pesticides; pharmaceutical agents of all types; consumer products such as macronutrients and food additives; environmental agents such as ambient ozone; and occupational exposures such as asbestos and benzene.
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