Pfizer Analytical Research and Development, Groton, CT.
Pfizer Analytical Research and Development, Chesterfield, MO.
J Immunol. 2023 Mar 15;210(6):764-773. doi: 10.4049/jimmunol.2100849.
Implementation of conjugate vaccine technology revolutionized the ability to effectively elicit long-lasting immune responses to bacterial capsular polysaccharides. Although expansion of conjugate vaccine serotype coverage is designed to target residual disease burden to pneumococcal serotypes not contained in earlier vaccine versions, details of polysaccharide Ag structure, heterogeneity, and epitope structure components contributing to vaccine-mediated immunity are not always clear. Analysis of Streptococcus pneumoniae serotype 12F polysaccharide by two-dimensional nuclear magnetic resonance spectroscopy and mass spectrometry revealed a partial substitution of N-acetyl-galactosamine by the keto sugar 2-acetamido-2,6-dideoxy-xylo-hexos-4-ulose (Sug) in up to 25% of the repeat units. This substitution was not described in previous published structures for 12F. Screening a series of contemporary 12F strains isolated from humans (n = 17) identified Sug incorporation at varying levels in all strains examined. Thus, partial Sug substitution in S. pneumoniae serotype 12F may have always been present but is now detectable by state-of-the-art analytical techniques. During the steps of conjugation, the serotype 12F Sug epitope is modified by reduction, and both polysaccharide PPSV23 and conjugate PCV20 vaccines contain 12F Ags with little to no Sug epitope. Both PCV20 and PPSV23 vaccines were evaluated for protection against circulating 12F strains with varying amounts of Sug in their repeat unit based on an opsonophagocytic killing assay involving HL-60 cells and rabbit complement. Both vaccines elicited human-derived neutralizing Abs against serotype 12F, independent of Sug level between ∼2 and 25 mol%. These findings suggest that the newly identified serotype 12F Sug epitope is likely not an essential epitope for vaccine-elicited protection.
结合疫苗技术的实施彻底改变了有效引发针对细菌荚膜多糖的长期免疫应答的能力。虽然结合疫苗血清型覆盖范围的扩大旨在针对不在早期疫苗版本中的肺炎球菌血清型的剩余疾病负担,但多糖 Ag 结构、异质性和有助于疫苗介导免疫的表位结构成分的细节并不总是清楚。通过二维核磁共振波谱和质谱分析肺炎链球菌血清型 12F 多糖,发现多达 25%的重复单元中,N-乙酰半乳糖胺被酮糖 2-乙酰氨基-2,6-二脱氧-木糖-4-ulose(Sug)部分取代。在以前发表的 12F 结构中没有描述这种取代。对从人类中分离的一系列当代 12F 菌株进行筛选,发现所有检测到的菌株中都存在不同水平的 Sug 掺入。因此,肺炎链球菌血清型 12F 中的部分 Sug 取代可能一直存在,但现在可以通过最先进的分析技术检测到。在结合步骤中,血清型 12F 的 Sug 表位被还原修饰,多糖 PPSV23 和结合疫苗 PCV20 都含有 12F Ag,几乎没有 Sug 表位。根据涉及 HL-60 细胞和兔补体的调理吞噬杀伤测定,对含有重复单元中不同数量 Sug 的循环 12F 菌株的 PCV20 和 PPSV23 疫苗进行了保护作用评估。两种疫苗都诱导了针对血清型 12F 的人源中和抗体,而 Sug 水平在 2 到 25 mol%之间变化。这些发现表明,新鉴定的血清型 12F Sug 表位可能不是疫苗诱导保护的必需表位。