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METHOD FOR THE PREPARATION OF CELLULAR CULTURAL INACTIVATED VACCINE AGAINST FOWL PEST

机译:一种针对原虫的细胞灭活疫苗的制备方法

摘要

The vaccine is inactivated by ethanol and is harmless. Theantigene for its preparation is produced after cultivation underroller conditions of the local cellular cultural strain DD/94 ofcells of the permanent line VIC21. The viral suspension producedwith infection titre 107.5 KID50 is adsorbed in 2% gel ofaliminium hydroxide and is settling for 48 h, after which thesupernatant is removed to 50% of the initial volume and isinactivated by ethanol. As an oleoadjuvant to the antigene mineraloil emulsified by montanide 888 is added in 3:2 ratio. Theimmunogeneity of the vaccine is tested on 18-20-week chicksimmunized with live vaccine in advance. On the 25th day after thevaccination a group of 10 chicks are infested by a virulent strainof the fowl pest virus. Simultaneoulsy a control group of 10unvaccined chicks is also infested. For 15 days 90% of thevaccined chicks remain in good health, and 90% of the controls diewith symptoms of fowl pest.2 claims.
机译:该疫苗被乙醇灭活,无害。在永久细胞系VIC21的局部细胞培养菌株DD / 94的滚动条件下培养后,产生用于制备其的抗原。将感染滴度为107.5 KID50的病毒悬浮液吸附在2%的氢氧化铵凝胶中,静置48小时,然后将上清液除去至初始体积的50%,并用乙醇灭活。作为蒙坦尼德888乳化的抗原矿物油的油佐剂,以3:2的比例加入。预先在已用活疫苗免疫的18-20周小鸡上测试疫苗的免疫原性。疫苗接种后第25天,有10只小鸡被家禽有害生物病毒的强毒株感染。同时感染了10只未接种疫苗的小鸡的对照组。在15天的时间里,90%的疫苗接种小鸡保持了良好的健康状态,而90%的对照者死于禽害。2

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