Choi Chan Woong, Moon Jae Hoon, Kim Jae Ok, Yoo Si Hyung, Kim Hyeon Guk, Kim Jung-Hwan, Park Tae Jun, Kim Sung Soon
Biologics Research Division, National Institute of Food and Drug Safety Evaluation, Cheongju, Korea.
Green Cross Research Center, Yongin, Korea.
Osong Public Health Res Perspect. 2018 Oct;9(5):278-282. doi: 10.24171/j.phrp.2018.9.5.10.
Vaccinations against diphtheria and tetanus are essential in providing immunity against these bacterial infections. The potency of diphtheria and tetanus toxoid vaccines can be measured using the in vivo toxin neutralization assay. The limit of potency of this assay was determined only for children. Therefore, we assessed the potency of adult vaccines using this assay to identify the feasibility of limit for adult vaccines.
Fifteen lots of tetanus-reduced diphtheria and tetanus-diphtheria-acellular pertussis vaccines were used. In vivo toxin neutralization and lethal challenge assays were conducted on each vaccine to calculate the potencies of the toxoids. National reference standards for toxins and antitoxins were used for in vivo toxin neutralization assay.
All 15 lots satisfied the limits of potency for lethal challenge assay. The potency of diphtheria and tetanus toxoids exceeded 1 and 8 units/mL, respectively, for in vivo toxin neutralization assay.
Although additional studies are required for new assays and limits, the current level of potency for adult vaccines as determined by in vivo toxin neutralization assay, was demonstrated in this study. Such efforts to improve assays are expected to promote the development of diphtheria and tetanus vaccines for adults and to contribute to vaccine self-sufficiency.
白喉和破伤风疫苗接种对于提供针对这些细菌感染的免疫力至关重要。白喉和破伤风类毒素疫苗的效力可通过体内毒素中和试验来测定。该试验的效力限度仅针对儿童确定。因此,我们使用此试验评估成人疫苗的效力,以确定成人疫苗效力限度的可行性。
使用了15批破伤风减量白喉和破伤风 - 白喉 - 无细胞百日咳疫苗。对每种疫苗进行体内毒素中和及致死性攻击试验,以计算类毒素的效力。体内毒素中和试验使用毒素和抗毒素的国家参考标准品。
所有15批疫苗均满足致死性攻击试验的效力限度。对于体内毒素中和试验,白喉和破伤风类毒素的效力分别超过1单位/毫升和8单位/毫升。
尽管新试验和限度需要更多研究,但本研究证明了通过体内毒素中和试验确定的成人疫苗当前效力水平。此类改进试验的努力有望促进成人白喉和破伤风疫苗的开发,并有助于实现疫苗自给自足。