Gao Fang, Lockyer Kay, Logan Alastair, Davis Sarah, Bolgiano Barbara, Rijpkema Sjoerd, Singh Gopal, Prasad Sai D, Dondapati Samuel Pradeep, Sounkhla Gurbaksh Singh
National Institute for Biological Standards and Control (NIBSC), South Mimms EN6 3QG, UK.
Bharat Biotech International Limited (BBIL), Hyderabad 500078, India.
Microorganisms. 2021 Aug 11;9(8):1707. doi: 10.3390/microorganisms9081707.
Typhoid conjugate vaccines (TCV) are effective in preventing enteric fever caused by serovar Typhi in Southeast Asia and Africa. To facilitate vaccination with the Vi capsular polysaccharide-tetanus toxoid conjugate vaccine, Typbar TCV, and allow it to be transported and stored outside a cold chain just prior to administration, an extended controlled-temperature conditions (ECTC) study was performed to confirm the quality of the vaccine at 40 °C for 3 days at the end of its shelf-life (36 months at 2-8 °C). Studies performed in parallel by the vaccine manufacturer, Bharat Biotech International Limited, and an independent national control laboratory (NIBSC) monitored its stability-indicating parameters: -acetylation of the Vi polysaccharide, integrity of the polysaccharide-protein conjugate, and its molecular size and pH. ECTC samples stored at 40 °C and 45 °C in comparison with control samples stored at 4 °C and 55 or 56 °C, were shown to have stable -acetylation and pH; only very slight increases in the percentage of free saccharide and corresponding decreases in molecular size were observed. The deoxycholate method for precipitating conjugated polysaccharide was very sensitive to small incremental increases in percentage of free saccharide, in line with storage temperature and duration. This extended ECTC study demonstrated minimal structural changes to the Vi polysaccharide and conjugate vaccine and a stable formulation following extended exposure to elevated temperatures for the desired durations. This outcome supports the manufacturer's ECTC claim for the vaccine to be allowed to be taken outside the cold chain before its administration.
伤寒结合疫苗(TCV)在预防东南亚和非洲由伤寒杆菌血清型引起的伤寒热方面有效。为了便于使用Vi荚膜多糖-破伤风类毒素结合疫苗Typbar TCV进行接种,并使其在接种前能在冷链外运输和储存,进行了一项扩展控温条件(ECTC)研究,以确认疫苗在保质期结束时(2-8℃下36个月)在40℃下放置3天的质量。疫苗生产商巴拉特生物技术国际有限公司和一个独立的国家对照实验室(NIBSC)并行开展的研究监测了其稳定性指示参数:Vi多糖的乙酰化、多糖-蛋白质结合物的完整性及其分子大小和pH值。与储存在4℃和55或56℃的对照样品相比,储存在40℃和45℃的ECTC样品显示出稳定的乙酰化和pH值;仅观察到游离糖百分比有非常轻微的增加以及分子大小相应减小。沉淀结合多糖的脱氧胆酸盐方法对游离糖百分比的微小增量增加非常敏感,这与储存温度和持续时间一致。这项扩展的ECTC研究表明,Vi多糖和结合疫苗的结构变化极小,在高温下延长暴露所需时间后制剂稳定。这一结果支持了生产商关于该疫苗在接种前可在冷链外使用的ECTC声明。