研讨会报告:评估拟作为常规食品成分的 Komagataella phaffii 中表达的重组人乳铁蛋白安全性的研究路线图--科学专家小组的建议。

IF 3.9 3区 医学 Q2 FOOD SCIENCE & TECHNOLOGY Food and Chemical Toxicology Pub Date : 2024-06-14 DOI:10.1016/j.fct.2024.114817
Carrie-Anne Malinczak , Leigh Ann Burns Naas , Anthony Clark , Dietrich Conze , Michael DiNovi , Norbert Kaminski , Claire Kruger , Bo Lönnerdal , Nicholas W. Lukacs , Robert Merker , Ross Peterson
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引用次数: 0

摘要

人乳乳铁蛋白(hmLF)是一种糖蛋白,对免疫功能的影响众所周知。Helaina 公司使用糖工程酵母 Komatagaella phaffii 生产重组人乳铁蛋白(Helaina rhLF,Effera™),其结构与 hmLF 相似,可用作食品配料。然而,由于安全性数据不足以及美国食品及药物管理局就口服 rhLF 的免疫原性/免疫毒性风险提出的安全性问题尚未得到解答,美国食品及药物管理局撤销了对 rhLF 的早期审查。Helaina 组织了一个由顶尖科学家组成的小组,以建立和审核一份安全性研究路线图,其中包含解决这些问题所需的研究和安全性终点。小组成员于 2023 年 6 月参加了为期一天的虚拟研讨会,并在 2023 年 7 月进行了讨论。研讨会的相关主题包括 LF 的理化特性、牛 LF 和 rhLF 作为 FDA 一般公认安全 (GRAS) 计划中的食品成分的监管历史,以及有关 rhLF 的免疫原性/alloimmunization、免疫毒理学、铁稳态以及吸收、分布、代谢和排泄的公开研究概要。专家小组成员得出结论认为,安全研究路线图解决了尚未解答的安全性问题,并实现了 rhLF 作为食品配料的预期安全使用,他们还同意将路线图广泛应用于评估其他具有免疫调节功能的重组乳蛋白的安全性并支持其 GRAS。
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Workshop report: A study roadmap to evaluate the safety of recombinant human lactoferrin expressed in Komagataella phaffii intended as an ingredient in conventional foods – Recommendations of a scientific expert panel

Human milk lactoferrin (hmLF) is a glycoprotein with well-known effects on immune function. Helaina Inc. has used a glycoengineered yeast, Komatagaella phaffii, to produce recombinant human lactoferrin (Helaina rhLF, Effera™) that is structurally similar to hmLF with intended uses as a food ingredient. However, earlier FDA reviews of rhLF were withdrawn due to insufficient safety data and unanswered safety questions the experts and FDA raised about the immunogenicity/immunotoxicity risks of orally ingested rhLF. Helaina organized a panel of leading scientists to build and vet a safety study roadmap containing the studies and safety endpoints needed to address these questions. Panelists participated in a one-day virtual workshop in June 2023 and ensuing discussions through July 2023. Relevant workshop topics included physicochemical properties of LF, regulatory history of bovine LF and rhLF as food ingredients in the FDA's generally recognized as safe (GRAS) program, and synopses of publicly available studies on the immunogenicity/alloimmunization, immunotoxicology, iron homeostasis, and absorption, distribution, metabolism, and excretion of rhLF. Panelists concluded that the safety study roadmap addresses the unanswered safety questions and the intended safe use of rhLF as a food ingredient for adults and agreed on broad applications of the roadmap to assess the safety and support GRAS of other recombinant milk proteins with immunomodulatory functions.

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来源期刊
Food and Chemical Toxicology
Food and Chemical Toxicology 工程技术-毒理学
CiteScore
10.90
自引率
4.70%
发文量
651
审稿时长
31 days
期刊介绍: Food and Chemical Toxicology (FCT), an internationally renowned journal, that publishes original research articles and reviews on toxic effects, in animals and humans, of natural or synthetic chemicals occurring in the human environment with particular emphasis on food, drugs, and chemicals, including agricultural and industrial safety, and consumer product safety. Areas such as safety evaluation of novel foods and ingredients, biotechnologically-derived products, and nanomaterials are included in the scope of the journal. FCT also encourages submission of papers on inter-relationships between nutrition and toxicology and on in vitro techniques, particularly those fostering the 3 Rs. The principal aim of the journal is to publish high impact, scholarly work and to serve as a multidisciplinary forum for research in toxicology. Papers submitted will be judged on the basis of scientific originality and contribution to the field, quality and subject matter. Studies should address at least one of the following: -Adverse physiological/biochemical, or pathological changes induced by specific defined substances -New techniques for assessing potential toxicity, including molecular biology -Mechanisms underlying toxic phenomena -Toxicological examinations of specific chemicals or consumer products, both those showing adverse effects and those demonstrating safety, that meet current standards of scientific acceptability. Authors must clearly and briefly identify what novel toxic effect (s) or toxic mechanism (s) of the chemical are being reported and what their significance is in the abstract. Furthermore, sufficient doses should be included in order to provide information on NOAEL/LOAEL values.
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