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Impact of the Conjugation Method on the Immunogenicity of Streptococcus pneumoniae Serotype 19F Polysaccharide in Conjugate Vaccines ▿

机译:结合方法对结合疫苗中肺炎链球菌血清型19F多糖免疫原性的影响▿

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摘要

7vCRM (Pfizer, Inc.) and PHiD-CV (GlaxoSmithKline Biologicals) are two pneumococcal conjugate vaccines licensed for the prevention of invasive pneumococcal disease and acute otitis media caused by the vaccine serotypes of Streptococcus pneumoniae. Neither vaccine contains serotype 19A, but both contain the closely related serotype 19F. No decrease in the incidence of serotype 19A disease has been observed following the introduction of 7vCRM, suggesting that this serotype 19F-containing vaccine provides limited cross-protection against serotype 19A. To investigate the impact that conjugation methods may have on antipolysaccharide immune responses and to determine whether this limited cross-protection is characteristic of the serotype 19F polysaccharide or rather of the 19F-CRM (cross-reacting material) conjugate, we compared naturally induced antibodies against serotypes 19F and 19A with antibodies induced after vaccination with different pneumococcal conjugate vaccines. We found that conjugation of the serotype 19F polysaccharide using reductive amination (as in 7vCRM) resulted in the formation of at least one additional epitope that is not present in the native form of the 19F polysaccharide or following 19F conjugation using a bifunctional spacer (as in the prototype vaccine 7vOMPC) or cyanylation (as in PHiD-CV). We also found that pneumococcal vaccines conjugated using cyanylation induce more opsonophagocytic antibodies against serotype 19F and a considerably higher level of cross-opsonophagocytic antibodies against serotype 19A than vaccines conjugated using reductive amination. In conclusion, these results suggest that the conjugation method can influence the functionality of the antibodies induced against the homologous serotype 19F and the cross-reactive serotype 19A of S. pneumoniae.
机译:7vCRM(Pfizer,Inc.)和PHiD-CV(GlaxoSmithKline Biologics)是两种肺炎球菌结合疫苗,被许可用于预防由肺炎链球菌疫苗血清型引起的侵袭性肺炎球菌疾病和急性中耳炎。两种疫苗均不含血清型19A,但均含有密切相关的血清型19F。引入7vCRM后,未观察到血清型19A疾病的发生率降低,这表明这种含血清型19F的疫苗对血清型19A的交叉保护作用有限。为了研究缀合方法可能对抗多糖免疫反应的影响并确定这种有限的交叉保护是血清型19F多糖还是19F-CRM(交叉反应材料)缀合物的特征,我们比较了天然诱导的抗用不同肺炎球菌结合疫苗接种后诱导产生的抗体的血清型19F和19A。我们发现使用还原性胺化作用(如7vCRM)对血清型19F多糖进行缀合会导致形成至少一种其他表位,该表位不存在于19F多糖的天然形式中,或者在使用双功能间隔子进行19F缀合后(如原型疫苗7vOMPC)或氰化(如在PHiD-CV中)。我们还发现,与使用还原胺化偶联的疫苗相比,使用氰基化偶联的肺炎球菌疫苗可诱导更多的针对血清19F的调理吞噬细胞抗体和针对针对19A血清型的交叉调理吞噬细胞抗体。总之,这些结果表明,结合方法可以影响针对肺炎链球菌的同源血清型19F和交叉反应血清型19A诱导的抗体的功能。

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