Giannelli C, Cappelletti E, Di Benedetto R, Pippi F, Arcuri M, Di Cioccio V, Martin L B, Saul A, Micoli F
GSK Vaccines Institute for Global Health S.r.l. (former Novartis Vaccines Institute for Global Health NVGH), Via Fiorentina 1, 53100 Siena, Italy.
GSK Vaccines Institute for Global Health S.r.l. (former Novartis Vaccines Institute for Global Health NVGH), Via Fiorentina 1, 53100 Siena, Italy.
J Pharm Biomed Anal. 2017 May 30;139:143-147. doi: 10.1016/j.jpba.2017.02.042. Epub 2017 Feb 24.
Glycoconjugate vaccines based on the Vi capsular polysaccharide directed against Salmonella enterica serovar Typhi are licensed or in development against typhoid fever, an important cause of morbidity and mortality in developing countries. Quantification of free polysaccharide in conjugate vaccines is an important quality control for release, to monitor vaccine stability and to ensure appropriate immune response. However, we found that existing separation methods based on size are not appropriate as free Vi non-specifically binds to unconjugated and conjugated protein. We developed a method based on free Vi separation by Capto Adhere resin and quantification by HPAEC-PAD. The method has been tested for conjugates of Vi derived from Citrobacter freundii with different carrier proteins such as CRM, Tetanus Toxoid and Diphtheria Toxoid.
基于伤寒杆菌Vi荚膜多糖的糖缀合物疫苗已获许可或正在研发,用于预防伤寒热,伤寒热是发展中国家发病和死亡的一个重要原因。定量测定结合疫苗中的游离多糖是疫苗放行的一项重要质量控制指标,用于监测疫苗稳定性并确保产生适当的免疫反应。然而,我们发现现有的基于大小的分离方法并不适用,因为游离Vi会非特异性地结合未结合和已结合的蛋白质。我们开发了一种基于用Capto Adhere树脂分离游离Vi并通过高效阴离子交换色谱-脉冲安培检测法进行定量的方法。该方法已针对来源于弗氏柠檬酸杆菌的Vi与不同载体蛋白(如CRM、破伤风类毒素和白喉类毒素)的缀合物进行了测试。