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药品中的β-葡聚糖污染:我们应该接受多少?

Beta-glucan contamination of pharmaceutical products: How much should we accept?

作者信息

Barton Claire, Vigor Kim, Scott Robert, Jones Paul, Lentfer Heike, Bax Heather J, Josephs Debra H, Karagiannis Sophia N, Spicer James F

机构信息

Cancer Research UK Centre for Drug Development, Cancer Research UK, Angel Building, 407 St John Street, London, EC1V 4AD, UK.

Biotherapeutics Development Unit, Cancer Research UK, South Mimms, Hertfordshire, EN6 3LD, UK.

出版信息

Cancer Immunol Immunother. 2016 Nov;65(11):1289-1301. doi: 10.1007/s00262-016-1875-9. Epub 2016 Jul 29.

Abstract

Beta-glucans are large polysaccharides produced by a range of prokaryotic and eukaryotic organisms. They have potential immunostimulatory properties and have been used with therapeutic intent as anti-microbial and anti-tumour agents. A range of other potentially beneficial effects have been described, and oral forms of beta-glucans are widely available over-the-counter and online. Parenteral formulations are popular in parts of Asia and are the subject of ongoing trials, worldwide. Beta-glucans are also potential contaminants of pharmaceutical products, and high levels have been described in some blood products. However, little is known about the clinical effects of such contamination, considerable uncertainty exists over the level at which immunostimulation may occur, and there are no guidelines available on acceptable levels. We encountered beta-glucan contamination of one of our products, and we suspect that others may encounter similar issues since the origin of beta-glucan contamination includes commonly used filters and solutions applied in the manufacture of biotherapeutic agents. It is likely that regulators will increasingly enquire about beta-glucan levels in pharmaceutical products, especially those with an immunomodulatory mechanism of action. Here, we review the literature on beta-glucans in pharmaceutical products and propose an acceptable level for therapeutic agents for parenteral use.

摘要

β-葡聚糖是由一系列原核生物和真核生物产生的大型多糖。它们具有潜在的免疫刺激特性,并已被用作抗菌和抗肿瘤药物用于治疗目的。还描述了一系列其他潜在的有益作用,并且口服形式的β-葡聚糖在非处方和在线渠道广泛可得。肠胃外制剂在亚洲部分地区很受欢迎,并且在全球范围内正在进行试验。β-葡聚糖也是药品的潜在污染物,在一些血液制品中已检测到高含量。然而,对于这种污染的临床影响知之甚少,关于免疫刺激可能发生的水平存在相当大的不确定性,并且没有关于可接受水平的指南。我们遇到了我们一种产品的β-葡聚糖污染,并且我们怀疑其他产品可能也会遇到类似问题,因为β-葡聚糖污染的来源包括生物治疗剂生产中常用的过滤器和溶液。监管机构很可能会越来越多地询问药品中的β-葡聚糖水平,尤其是那些具有免疫调节作用机制的药品。在此,我们综述了关于药品中β-葡聚糖的文献,并提出了肠胃外使用治疗剂的可接受水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f04d/11028623/1ef728c55cc2/262_2016_1875_Fig1_HTML.jpg

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