免疫安全化身概述:模拟免疫调节疗法对免疫系统的影响。

IF 2.4 4区 医学 Q3 TOXICOLOGY Journal of Immunotoxicology Pub Date : 2024-10-01 Epub Date: 2024-12-10 DOI:10.1080/1547691X.2024.2354213
Vanessa Neuhaus, Laure-Alix Clerbaux, Katherina Sewald
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引用次数: 0

摘要

像调节免疫系统的生物制剂这样的创新疗法正在兴起。然而,它们的免疫调节特性有时也会引发意想不到的免疫反应,从而导致不良反应的产生。由于这些治疗方法的复杂性和靶标特异性,如果测试系统是基于动物的,这些药物引起的不良事件可能在非临床开发期间仍未被发现,并且只有在人体试验时才出现在临床开发中,随后导致原本有希望的候选药物停产。为了在早期阶段识别对人体免疫系统的不良影响,需要新的方法、分析方法和技术。创新医学倡议(IMI)合作的免疫安全化身(imSAVAR)项目旨在开发一种工具,用于免疫调节新治疗药物和临床试验应用的综合非临床安全性评估。为了实现这一目标,imSAVAR依靠不良后果途径(AOP)框架以结构化的方法收集知识,并在需要时设计、选择或开发适当的测试系统,以预测免疫相关的不良后果。到目前为止,imSAVAR联盟已经确定了需要改进风险评估的某些类别药物的“作用模式”,包括嵌合抗原受体T细胞(CAR - T细胞)、免疫检查点抑制剂(ICIs)和重组蛋白(如白细胞介素[IL]-2),并将这些药物与免疫相关的不良后果联系起来,并制定了基于文献的免疫相关AOPs (irAOPs)。测量这些免疫特异性扰动的模型被选择、调整或新开发。《免疫毒理学杂志》特刊中描述的imSAVAR工作支持我们对免疫介导的不良反应的理解,以及在开发过程中的早期发现,以提高创新生物医药的安全性。
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An overview of immune safety avatar: mimicking the effects of immunomodulatory therapies on the immune system.

Innovative therapeutics like biologicals that modulate the immune system are on the rise. However, their immune-modulating characteristics can also lead sometimes to the induction of adverse effects, by triggering unintended immune reactions. Due to the complexity and target-specificity of such therapeutics, these drug-induced adverse events could remain undetected during non-clinical development, if the test systems are, for example, animal-based, and only emerge in clinical development when tested in humans and subsequently lead to discontinuance of otherwise promising drug candidates. To identify adverse effects on the human immune system at an early stage, new approaches, assays, and technologies are needed. The Innovative Medicine Initiative (IMI) cooperation Immune Safety Avatar (imSAVAR) project aims to develop a tool for integrated non-clinical safety assessment for immune-modulatory new therapeutic drugs and clinical trial applications. To achieve this goal, imSAVAR has relied on the Adverse Outcome Pathway (AOP) framework to gather knowledge in a structured approach and to design, select or develop, when needed, appropriate test systems for prediction of the immune-related adverse outcomes. So far, the imSAVAR consortium has identified the "mode of action" for certain classes of drugs that needed improved risk assessment, including chimeric antigen receptor T cells (CAR T cells), immune checkpoint inhibitors (ICIs), and recombinant proteins (e.g. interleukin [IL]-2), has linked those to their immune-related adverse outcomes and has formulated literature-based immune-related AOPs (irAOPs). Models to measure those immune-specific perturbations were selected, adjusted, or newly developed. The imSAVAR work described in this special issue of The Journal of Immunotoxicology supports our understanding of immune-mediated adverse effects and their early discovery during development to improve the safety of innovative biomedicals.

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来源期刊
Journal of Immunotoxicology
Journal of Immunotoxicology 医学-毒理学
CiteScore
6.70
自引率
3.00%
发文量
26
审稿时长
1 months
期刊介绍: The Journal of Immunotoxicology is an open access, peer-reviewed journal that provides a needed singular forum for the international community of immunotoxicologists, immunologists, and toxicologists working in academia, government, consulting, and industry to both publish their original research and be made aware of the research findings of their colleagues in a timely manner. Research from many subdisciplines are presented in the journal, including the areas of molecular, developmental, pulmonary, regulatory, nutritional, mechanistic, wildlife, and environmental immunotoxicology, immunology, and toxicology. Original research articles as well as timely comprehensive reviews are published.
期刊最新文献
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