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肺炎球菌结合疫苗成分热稳定性的物理化学评估

A physico-chemical assessment of the thermal stability of pneumococcal conjugate vaccine components.

作者信息

Gao Fang, Lockyer Kay, Burkin Karena, Crane Dennis T, Bolgiano Barbara

机构信息

a Division of Bacteriology ; National Institute for Biological Standards and Control ; Hertfordshire , UK.

出版信息

Hum Vaccin Immunother. 2014;10(9):2744-53. doi: 10.4161/hv.29696. Epub 2014 Nov 17.

Abstract

Physico-chemical analysis of pneumococcal polysaccharide (PS)-protein conjugate vaccine components used for two commercially licensed vaccines was performed to compare the serotype- and carrier protein-specific stabilities of these vaccines. Nineteen different monovalent pneumococcal conjugates from commercial vaccines utilizing CRM197, diphtheria toxoid (DT), Protein D (PD) or tetanus toxoid (TT) as carrier proteins were incubated at temperatures up to 56°C for up to eight weeks or were subjected to freeze-thawing (F/T). Structural stability was evaluated by monitoring their size, integrity and carrier protein conformation. The molecular size of the vaccine components was well maintained for Protein D, TT and DT conjugates at -20°C, 4°C and F/T, and for CRM197 conjugates at 4°C and F/T. It was observed that four of the eight serotypes of Protein D conjugates tended to form high molecular weight complexes at 37°C or above. The other conjugated carrier proteins also appeared to form oligomers or 'aggregates' at elevated temperatures, but rarely when frozen and thawed. There was evidence of degradation in some of the conjugates as evidenced by the formation of lower molecular weight materials which correlated with measured free saccharide. In conclusion, pneumococcal-Protein D/TT/DT and most CRM197 bulk conjugate vaccines were stable when stored at 2-8°C, the recommended temperature. In common between the conjugates produced by the two manufacturers, serotypes 1, 5, and 19F were relatively less stable and 6B was the most stable, with types 7F and 23F also showing good stability.

摘要

对两种商业许可疫苗中使用的肺炎球菌多糖(PS)-蛋白质结合疫苗成分进行了物理化学分析,以比较这些疫苗的血清型和载体蛋白特异性稳定性。利用CRM197、白喉类毒素(DT)、D蛋白(PD)或破伤风类毒素(TT)作为载体蛋白,对来自商业疫苗的19种不同单价肺炎球菌结合物在高达56°C的温度下孵育长达8周,或进行冻融(F/T)处理。通过监测其大小、完整性和载体蛋白构象来评估结构稳定性。对于D蛋白、TT和DT结合物,在-20°C、4°C和冻融条件下,以及对于CRM197结合物在4°C和冻融条件下,疫苗成分的分子大小得到了很好的维持。观察到,8种血清型的D蛋白结合物中有4种在37°C或更高温度下倾向于形成高分子量复合物。其他结合的载体蛋白在温度升高时也似乎形成寡聚物或“聚集体”,但在冻融时很少出现这种情况。有证据表明,一些结合物发生了降解,表现为形成了与测得的游离糖相关的低分子量物质。总之,肺炎球菌-D蛋白/TT/DT和大多数CRM197批量结合疫苗在2-8°C(推荐温度)储存时是稳定的。两家制造商生产的结合物的共同之处在于,血清型1、5和19F相对不太稳定,6B最稳定,7F和23F型也表现出良好的稳定性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4931/4977451/08935b37ea00/khvi-10-09-970924-g001.jpg

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