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Molecular effects of polystyrene nanoplastics on human neural stem cells.聚苯乙烯纳米塑料对人神经干细胞的分子影响。
PLoS One. 2024 Jan 3;19(1):e0295816. doi: 10.1371/journal.pone.0295816. eCollection 2024.
2
Design of an Ara h 2 hypoallergen from conformational epitopes.设计一种 Ara h 2 变应原,基于构象表位。
Clin Exp Allergy. 2024 Jan;54(1):46-55. doi: 10.1111/cea.14433. Epub 2024 Jan 2.
3
Widespread monoclonal IgE antibody convergence to an immunodominant, proanaphylactic Ara h 2 epitope in peanut allergy.花生过敏中广泛存在的单克隆 IgE 抗体向免疫显性、致过敏的 Ara h 2 表位趋同。
J Allergy Clin Immunol. 2024 Jan;153(1):182-192.e7. doi: 10.1016/j.jaci.2023.08.035. Epub 2023 Sep 23.
4
Innovative tools and methods for toxicity testing within PARC work package 5 on hazard assessment.PARC工作包5中关于危害评估的毒性测试创新工具和方法。
Front Toxicol. 2023 Jul 19;5:1216369. doi: 10.3389/ftox.2023.1216369. eCollection 2023.
5
Suspended hydrogel culture as a method to scale up intestinal organoids.悬浮水凝胶培养作为一种规模化肠道类器官的方法。
Sci Rep. 2023 Jun 27;13(1):10412. doi: 10.1038/s41598-023-35657-9.
6
Dietary exposure to endocrine disruptors in gut microbiota: A systematic review.饮食中内源性干扰物对肠道微生物群的影响:系统综述。
Sci Total Environ. 2023 Aug 15;886:163991. doi: 10.1016/j.scitotenv.2023.163991. Epub 2023 May 9.
7
FDA-approved drug screening in patient-derived organoids demonstrates potential of drug repurposing for rare cystic fibrosis genotypes.在患者衍生类器官中进行 FDA 批准药物筛选,为罕见囊性纤维化基因型的药物再利用提供了潜力。
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Shiga Toxin (Stx) Type 1a and Stx2a Translocate through a Three-Layer Intestinal Model.志贺毒素(Stx)1a 型和 Stx2a 通过三层肠模型转运。
Toxins (Basel). 2023 Mar 9;15(3):207. doi: 10.3390/toxins15030207.
9
Animal Models for the Study of Food Allergies.食物过敏研究的动物模型。
Curr Protoc. 2023 Mar;3(3):e685. doi: 10.1002/cpz1.685.
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Poor Translatability of Biomedical Research Using Animals - A Narrative Review.使用动物进行生物医学研究的翻译难度大——一篇叙述性综述
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相信你的直觉:建立对胃肠道模型的信心——科学现状和应用背景概述。

Trust your gut: Establishing confidence in gastrointestinal models - An overview of the state of the science and contexts of use.

机构信息

SJD Consulting LLC, Ijamsville, MD, USA.

Inotiv, Inc., RTP, NC, USA.

出版信息

ALTEX. 2024;41(3):402-424. doi: 10.14573/altex.2403261. Epub 2024 May 15.

DOI:10.14573/altex.2403261
PMID:38898799
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11413798/
Abstract

The webinar series and workshop titled “Trust Your Gut: Establishing Confidence in Gastrointestinal Models – An Overview of the State of the Science and Contexts of Use” was co-organized by NICEATM, NIEHS, FDA, EPA, CPSC, DoD, and the Johns Hopkins Center for Alternatives to Animal Testing (CAAT) and hosted at the National Institutes of Health in Bethesda, MD, USA on October 11-12, 2023. New approach methods (NAMs) for assessing issues of gastrointestinal tract (GIT)- related toxicity offer promise in addressing some of the limitations associated with animal-based assessments. GIT NAMs vary in complexity, from two-dimensional monolayer cell line-based systems to sophisticated 3-dimensional organoid systems derived from human primary cells. Despite advances in GIT NAMs, challenges remain in fully replicating the complex interactions and pro­cesses occurring within the human GIT. Presentations and discussions addressed regulatory needs, challenges, and innovations in incorporating NAMs into risk assessment frameworks; explored the state of the science in using NAMs for evaluating systemic toxicity, understanding absorption and pharmacokinetics, evaluating GIT toxicity, and assessing potential allergenicity; and discussed strengths, limitations, and data gaps of GIT NAMs as well as steps needed to establish confidence in these models for use in the regulatory setting.

摘要

本次网络研讨会系列和研讨会的标题为“相信你的直觉:在胃肠道模型中建立信心——科学现状和使用背景概述”,由 NICEATM、NIEHS、FDA、EPA、CPSC、DoD 和约翰霍普金斯替代动物测试中心(CAAT)共同组织,并于 2023 年 10 月 11 日至 12 日在美国马里兰州贝塞斯达的美国国立卫生研究院举行。用于评估胃肠道(GIT)相关毒性问题的新方法(NAMs)在解决与基于动物的评估相关的一些限制方面具有很大的应用前景。GIT NAMs 的复杂性各不相同,从二维单层细胞系系统到源自人类原代细胞的复杂 3 维类器官系统。尽管 GIT NAMs 取得了进展,但在完全复制人类 GIT 内发生的复杂相互作用和过程方面仍存在挑战。演讲和讨论涉及将 NAMs 纳入风险评估框架的监管需求、挑战和创新;探讨了使用 NAMs 评估系统毒性、了解吸收和药代动力学、评估 GIT 毒性以及评估潜在致敏性的科学现状;并讨论了 GIT NAMs 的优势、局限性和数据差距,以及在监管环境中使用这些模型建立信心所需的步骤。