Collaborative study for the establishment of a candidate equine influenza subtype 2 American-like strain A/EQ/South Africa/4/03 - horse antiserum biological reference preparation.

Pharmeuropa bio Pub Date : 2007-12-01
Janet Daly, A Daas, M-E Behr-Gross
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Abstract

In 2004, the Office International des Epizooties (OIE) Expert Surveillance Panel on equine influenza recommended that the American lineage component (H3N8) of equine influenza vaccines (A/eq/Newmarket/1/93-like) be updated to an A/eq/South Africa/4/03-like virus. As a consequence the common European Pharmacopoeia (Ph. Eur.) - OIE reference for equine influenza subtype 2 American-like antiserum had to be complemented by an antiserum raised in horses against an A/eq/South Africa/4/03 strain. An international collaborative study run by the European Directorate for the Quality of Medicines (EDQM) in the frame of its Biological Standardisation Programme (BSP) under the aegis of the Ph. Eur. and the OIE was organised. The study was aimed at evaluating a candidate reference horse anti-serum using the single radial haemolysis (SRH) and haemagglutination inhibition (HI) tests. The standard was to be established for use in immunogenicity and batch potency assay of equine influenza vaccines as a Ph. Eur. BRP and for use in clinical diagnostic tests as an OIE-approved International Standard. The evaluation performed in the collaborative study enabled the suitability of the candidate to be demonstrated and an SRH value to be 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 June and September 2006, respectively.

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合作研究建立候选马流感2亚型美国样菌株a/ EQ/南非/4/03 -马抗血清生物参比制剂。
2004年,国际兽疫局(OIE)马流感专家监测小组建议将马流感疫苗(A/eq/Newmarket/1/93-like)的美国谱系成分(H3N8)更新为A/eq/South Africa/4/03-like病毒。因此,欧洲药典(Ph. Eur.) -世界动物卫生组织(OIE)对马流感2亚型美国样抗血清的参考资料必须由在马体内培养的抗a/ eq/南非/4/03菌株的抗血清补充。由欧洲药品质量理事会(EDQM)在其生物标准化计划(BSP)框架内开展的一项国际合作研究。世界动物卫生组织成立了。该研究旨在通过单放射状溶血(SRH)和血凝抑制(HI)试验评估候选参考马抗血清。本标准用于马流感疫苗的免疫原性和批量效价测定。BRP和作为世界动物卫生组织批准的国际标准用于临床诊断试验。在合作研究中进行的评估能够证明候选人的适用性,并分配SRH值。该候选人已被欧盟理事会通过为BRP。并分别于2006年6月和9月获世界动物卫生组织生物标准委员会批准为国际标准血清。
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