Establishment of a candidate equine influenza Florida Clade 2 strain A/eq/Richmond/1/07 horse antiserum as Ph. Eur. Biological Reference Preparation/OIE International Reference Reagent.

Q4 Medicine
Pharmeuropa bio & scientific notes Pub Date : 2020-01-01
R Paillot, E Regourd, M-E Behr-Gross
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引用次数: 0

Abstract

Equine influenza (EI) is an important respiratory disease of horses, with welfare and economic consequences. Vaccination remains one of the most efficient prevention methods available. Equine influenza virus (EIV) is constantly evolving and consequently EI vaccines need to be updated on a regular basis. In 2010, the World Organisation for Animal Health (OIE) Expert Surveillance Panel (ESP) on EI provided a new recommendation for EI vaccine strain composition, including the incorporation of representative EIV strains of both Florida Clade 1 and Clade 2 sub-lineages (FC1 and FC2, respectively). In this context, the European Pharmacopoeia (Ph. Eur.) - OIE reference panel for EI had to be complemented by an antiserum raised in horses against the FC2 representative EIV strain A/eq/Richmond/1/07. An international collaborative study was organised and managed by the European Directorate for the Quality of Medicines and HealthCare (EDQM) within the framework of its Biological Standardisation Programme (BSP). The study aimed at evaluating a new candidate reference for use as a common OIE International Standard/Ph. Eur. Biological Reference Preparation (BRP) horse antiserum to FC2 EIV A/equine/Richmond/1/07. The standard was to be established using the SRH and HI tests for subsequent use in immunogenicity, efficacy and batch potency assay of EI vaccines as a Ph. Eur. BRP (Ph. Eur. monograph 0249) and for use in clinical diagnostic tests as an OIE-approved International Standard Reagent (OIE chapter 3.5.7). The collaborative study confirmed the suitability of the candidate and an SRH titre was assigned. The candidate was adopted as a BRP by the Ph. Eur. Commission and approved by the OIE Biological Standards Commission as an International Standard Serum in November 2017 and February 2018, respectively.

马流感候选菌株a /eq/Richmond/1/07抗血清的建立。生物标准制剂/OIE国际标准试剂。
马流感(EI)是一种重要的马呼吸道疾病,具有严重的福利和经济后果。疫苗接种仍然是最有效的预防方法之一。马流感病毒(EIV)不断演变,因此需要定期更新EI疫苗。2010年,世界动物卫生组织(OIE) EI专家监测小组(ESP)对EI疫苗毒株组成提出了新的建议,包括纳入佛罗里达进化枝1和进化枝2亚谱系(分别为FC1和FC2)的代表性EIV毒株。在这种情况下,欧洲药典(Ph. Eur.) -世界动物卫生组织EI参考小组必须通过在马中培养抗FC2代表性EIV菌株A/eq/Richmond/1/07的抗血清来补充。欧洲药品和保健质量理事会(EDQM)在其生物标准化计划(BSP)框架内组织和管理了一项国际合作研究。本研究旨在评估一种新的候选参考标准,作为世界动物卫生组织国际标准/Ph。欧元。生物参比制剂(BRP)马抗血清FC2 EIV A/马/Richmond/1/07。该标准将使用SRH和HI试验建立,用于随后作为Ph. Eur的EI疫苗的免疫原性、有效性和批量效力测定。Ph. Eur;专著0249),并作为世界动物卫生组织批准的国际标准试剂用于临床诊断试验(世界动物卫生组织第3.5.7章)。合作研究证实了候选人的适宜性,并分配了一个SRH滴度。该候选人已被欧盟理事会通过为BRP。分别于2017年11月和2018年2月被世界动物卫生组织生物标准委员会批准为国际标准血清。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Pharmeuropa bio & scientific notes
Pharmeuropa bio & scientific notes Medicine-Medicine (all)
CiteScore
0.70
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