Suppr超能文献

在中国使用微载体技术生产和评价色谱纯化的狂犬病疫苗(PVRV)。

Production and evaluation of a chromatographically purified Vero cell rabies vaccine (PVRV) in China using microcarrier technology.

机构信息

State Key Laboratory for Infectious Disease Prevention and Control, Institute for Viral Disease Control and Prevention, Beijing, PR China.

出版信息

Hum Vaccin Immunother. 2012 Sep;8(9):1230-5. doi: 10.4161/hv.20985. Epub 2012 Aug 16.

Abstract

China is a high population country with millions of animal bite cases every year; thus, it is necessary to explore and develop more effective and productive rabies vaccines for human use. To establish a safe, effective, inexpensive and high-yield rabies vaccine, a non-adjuvant purified Vero cell rabies vaccine produced in the SPEEDA PVRV microcarrier bioreactor was developed by Liaoning Chengda Biology Co. Ltd. in China. This vaccine was produced using Vero cells that were cultured in a microcarrier bioreactor. A microcarrier bioreactor containing 25 g/L of Cytodex-1 was used for perfusion culture. The Vero cell culture density was up to 1.2-1.5 × 10(7) cells/ml, viruses could be constantly harvested for 18-22 days, and the resulting vaccine immunizing potency was ≥ 4.5 IU/ml. Vaccine safety and immunogenicity post-immunization were also assessed. A total of 602 volunteers were enrolled and divided into two groups that were vaccinated with either SPEEDA PVRV or VERORAB PVRV on days 0, 3, 7, 14 and 28. All subjects vaccinated with SPEEDA PVRV showed no serious local or systemic adverse effects. The positive conversion rate of serum neutralizing antibodies against the rabies virus reached 100% in both the test and control groups (inoculated with VERORAB PVRV) at 14 days and 45 days after vaccination, and no significant difference was found between the neutralizing antibody geometric mean titers (GMTs) of the two groups. SPEEDA PVRV is appropriate for mass production and shows satisfactory clinical safety and immunogenicity for human post-exposure prophylaxis of rabies.

摘要

中国是一个人口众多的国家,每年有数百万人被动物咬伤;因此,有必要探索和开发更有效、更有生产力的狂犬病疫苗供人类使用。为了建立一种安全、有效、廉价和高产量的狂犬病疫苗,中国辽宁成大生物股份有限公司利用 SPEEDA PVRV 微载体生物反应器开发了一种无佐剂纯化的 Vero 细胞狂犬病疫苗。该疫苗使用在微载体生物反应器中培养的 Vero 细胞生产。使用含有 25 g/L Cytodex-1 的微载体生物反应器进行灌注培养。Vero 细胞培养密度高达 1.2-1.5×10(7)细胞/ml,可连续收获病毒 18-22 天,得到的疫苗免疫效力≥4.5 IU/ml。还评估了疫苗接种后的安全性和免疫原性。共纳入 602 名志愿者,分为两组,分别于第 0、3、7、14 和 28 天接种 SPEEDA PVRV 或 VERORAB PVRV。所有接种 SPEEDA PVRV 的受试者均未出现严重的局部或全身不良反应。两组受试者在接种后 14 天和 45 天,血清中针对狂犬病病毒的中和抗体阳性转化率均达到 100%(接种 VERORAB PVRV),两组的中和抗体几何平均滴度(GMT)无显著差异。SPEEDA PVRV 适合大规模生产,对狂犬病暴露后人类预防具有良好的临床安全性和免疫原性。

相似文献

引用本文的文献

10
Advances in cell culture: anchorage dependence.细胞培养的进展:贴壁依赖性
Philos Trans R Soc Lond B Biol Sci. 2015 Feb 5;370(1661):20140040. doi: 10.1098/rstb.2014.0040.

本文引用的文献

1
[Epidemiological analysis of rabies in 2010, China].[2010年中国狂犬病流行病学分析]
Zhonghua Shi Yan He Lin Chuang Bing Du Xue Za Zhi. 2011 Dec;25(6):434-6.
4
WHO Expert Consultation on rabies.世界卫生组织狂犬病专家磋商会
World Health Organ Tech Rep Ser. 2005;931:1-88, back cover.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验