Development of a new 15-valent pneumococcal conjugate vaccine (PCV15) and evaluation of its immunogenicity

免疫原性 血清型 佐剂 肺炎球菌结合疫苗 微生物学 抗体效价 肺炎链球菌 抗体 结合疫苗 结合 效价 生物 病毒学 免疫学 抗生素 数学分析 数学
作者
Chankyu Lee,Seo‐Hyun Choi,Rock Ki Kim,Hee-Youn Kim,Yoon Hee Whang,Huyen Pharm,Hyunwoo Cheon,Do Young Yoon,Chan Wha Kim,Yeong Ok Baik,Sung Soo Park,Inhwan Lee
出处
期刊:Biologicals [Elsevier BV]
卷期号:61: 32-37 被引量:9
标识
DOI:10.1016/j.biologicals.2019.07.005
摘要

A new 15-valent pneumococcal conjugate vaccine (PCV15) against serotypes 1, 3, 4, 5, 6A, 6B, 7F, 9V, 11A, 14, 18C, 19A, 19F, 22F, and 23F has been developed using aluminum phosphate as an adjuvant. Using the rabbit model, immunogenicity of each serotype was evaluated by measuring antigen specific antibodies and functional antibody titers and comparing them to a control vaccine, Prevnar13®. Among the shared serotypes in both PCV15 and Prevnar13®, Type 3 and 23F in PCV15 exhibited a lower opsonic index than Prevnar13®. Conversely, the other types showed greater or nearly the same immunogenic effects. Type 11A and 22F are two additional serotypes included in PCV15, and only 22F showed a reasonable opsonic index compared with other types. Type 11A exhibited a basal level fold-increase in OPA; thus, we further optimized 11A as well as 3 and 23F by controlling the polysaccharide-to-protein conjugation ratio as a variable. Antibody levels and functional antibody activities were evaluated by ELISA and OPA, and improved levels of immunogenic activities were observed for all three serotypes. In this study, we propose a new PCV15 candidate, in which the common 13 serotypes and a licensed control vaccine have equivalent efficacy while two additional serotypes showed adequate immunogenicity in the rabbit model.

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