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本文引用的文献

1
Challenges and approaches for the development of safer immunomodulatory biologics.免疫调节生物制剂安全性开发面临的挑战与对策
Nat Rev Drug Discov. 2013 Apr;12(4):306-24. doi: 10.1038/nrd3974.
2
Monitoring drug safety with registries: useful components of postmarketing pharmacovigilance systems.利用登记处监测药物安全性:上市后药物警戒系统的有用组成部分。
J Clin Epidemiol. 2012 Feb;65(2):121-5. doi: 10.1016/j.jclinepi.2011.06.017. Epub 2011 Oct 8.

2012 年 AAPS 国家生物技术会议公开论坛:对当前免疫原性预测和风险管理现状的看法。

2012 AAPS National Biotech Conference Open Forum: a perspective on the current state of immunogenicity prediction and risk management.

机构信息

Bioanalytical Sciences, Regeneron Pharmaceuticals Inc, Tarrytown, New York, USA,

出版信息

AAPS J. 2013 Oct;15(4):1155-9. doi: 10.1208/s12248-013-9520-4. Epub 2013 Aug 30.

DOI:10.1208/s12248-013-9520-4
PMID:23990501
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3787208/
Abstract

The immunogenicity profile of a biotherapeutic is determined by multiple product-, process- or manufacturing-, patient- and treatment-related factors and the bioanalytical methodology used to monitor for immunogenicity. This creates a complex situation that limits direct correlation of individual factors to observed immunogenicity rates. Therefore, mechanistic understanding of how these factors individually or in concert could influence the overall incidence and clinical risk of immunogenicity is crucial to provide the best benefit/risk profile for a given biotherapeutic in a given indication and to inform risk mitigation strategies. Advances in the field of immunogenicity have included development of best practices for monitoring anti-drug antibody development, categorization of risk factors contributing to immunogenicity, development of predictive tools, and development of effective strategies for risk management and mitigation. Thus, the opportunity to ask "where we are now and where we would like to go from here?" was the main driver for organizing an Open Forum on Improving Immunogenicity Risk Prediction and Management, conducted at the 2012 American Association of Pharmaceutical Scientists' (AAPS) National Biotechnology Conference in San Diego. The main objectives of the Forum include the following: to understand the nature of immunogenicity risk factors, to identify analytical tools used and animal models and management strategies needed to improve their predictive value, and finally to identify collaboration opportunities to improve the reliability of risk prediction, mitigation, and management. This meeting report provides the Forum participant's and author's perspectives on the barriers to advancing this field and recommendations for overcoming these barriers through collaborative efforts.

摘要

生物治疗药物的免疫原性特征由多种产品、工艺或生产、患者和治疗相关因素以及用于监测免疫原性的生物分析方法决定。这造成了一种复杂的情况,限制了将个别因素与观察到的免疫原性发生率直接相关联。因此,深入了解这些因素如何单独或协同影响免疫原性的总体发生率和临床风险,对于在特定适应症下为特定生物治疗药物提供最佳的获益/风险比,并为风险缓解策略提供信息至关重要。免疫原性领域的进展包括开发监测抗药物抗体产生的最佳实践、对导致免疫原性的风险因素进行分类、开发预测工具以及开发有效的风险管理和缓解策略。因此,有机会提出“我们现在在哪里,我们希望从这里走向何方?”是在圣地亚哥举行的 2012 年美国药物科学家协会(AAPS)国家生物技术会议上组织关于改善免疫原性风险预测和管理的开放式论坛的主要驱动力。该论坛的主要目标包括:了解免疫原性风险因素的性质,确定用于提高其预测价值的分析工具、动物模型和管理策略,并最终确定合作机会以提高风险预测、缓解和管理的可靠性。本会议报告提供了论坛参与者和作者对推进该领域的障碍的看法,并提出了通过合作努力克服这些障碍的建议。