Research and External Innovation, Sanofi Pasteur, Marcy l'Etoile, France.
Analytical Sciences, Sanofi Pasteur, Marcy l'Etoile, France.
Vaccine. 2021 Mar 26;39(13):1846-1856. doi: 10.1016/j.vaccine.2021.02.033. Epub 2021 Mar 6.
Yellow fever (YF) remains a threat to human health in tropical regions of Africa and South America. Live-attenuated YF-17D vaccines have proven to be safe and effective in protecting travellers and populations in endemic regions against YF, despite very rare severe reactions following vaccination - YF vaccine-associated viscerotropic disease (YEL-AVD) and neurological disease (YEL-AND). We describe the generation and selection of a live-attenuated YF-17D vaccine candidate and present its preclinical profile. Initially, 24 YF-17D vaccine candidate sub-strains from the Stamaril® and YF-VAX® lineage were created through transfection of viral genomic RNA into Vero cells cultured in serum-free media to produce seed lots. The clone with the 'optimal' preclinical profile, i.e. the lowest neurovirulence, neurotropism and viscerotropism, and immunogenicity at least comparable with Stamaril and YF-VAX in relevant animal models, was selected as the vaccine candidate and taken forward for assessment at various production stages. The 'optimal' vaccine candidate was obtained from the YF-VAX lineage (hence named vYF-247) and had five nucleotide differences relative to its parent, with only two changes that resulted in amino acid changes at position 480 of the envelope protein (E) (valine to leucine), and position 65 of the non-structural protein 2A (NS2A) (methionine to valine). vYF-247 was less neurovirulent in mice than Stamaril and YF-VAX irrespective of production stage. Its attenuation profile in terms of neurotropism and viscerotropism was similar to YF-VAX in A129 mice, a 'worst case' animal model lacking type-I IFN receptors required to initiate viral clearance. Thus, vYF-247 would not be expected to have higher rates of YEL-AVD or YEL-AND than Stamaril and YF-VAX. In hamsters, vYF-247 was immunogenic and protected against high viremia and death induced by a lethal challenge with the hamster-adapted Jimenez P10 YF virus strain. Our data suggests that vYF-247 would provide robust protection against YF disease in humans, similar to currently marketed YF vaccines.
黄热病(YF)仍然是非洲和南美洲热带地区人类健康的威胁。尽管接种后极少数情况下会出现严重反应,即黄热病疫苗相关内脏病(YEL-AVD)和神经系统疾病(YEL-AND),但减毒活疫苗 YF-17D 已被证明在保护旅行者和流行地区人群免受 YF 方面是安全有效的。我们描述了一种减毒活 YF-17D 疫苗候选物的产生和选择,并介绍了其临床前概况。最初,通过将病毒基因组 RNA 转染到无血清培养基中培养的 Vero 细胞中,从 Stamaril®和 YF-VAX®系产生了 24 种 YF-17D 候选疫苗亚株,以产生种子批次。选择具有“最佳”临床前特征的克隆,即神经毒力、神经嗜性和内脏嗜性最低,以及在相关动物模型中与 Stamaril 和 YF-VAX 至少相当的免疫原性,作为候选疫苗,并在各个生产阶段进行评估。“最佳”疫苗候选物来自 YF-VAX 系(因此命名为 vYF-247),与亲本相比有五个核苷酸差异,只有两个变化导致包膜蛋白(E)位置 480 的氨基酸(缬氨酸变为亮氨酸)和非结构蛋白 2A(NS2A)位置 65 的氨基酸(蛋氨酸变为缬氨酸)发生变化。无论生产阶段如何,vYF-247 在小鼠中的神经毒力均低于 Stamaril 和 YF-VAX。在缺乏启动病毒清除所需的 I 型干扰素受体的“最坏情况”动物模型 A129 小鼠中,其神经嗜性和内脏嗜性的衰减特征与 YF-VAX 相似。因此,vYF-247 不太可能比 Stamaril 和 YF-VAX 具有更高的 YEL-AVD 或 YEL-AND 发生率。在仓鼠中,vYF-247 具有免疫原性,可预防由仓鼠适应的 Jimenez P10 YF 病毒株引起的高病毒血症和死亡。我们的数据表明,vYF-247 将为人类提供针对 YF 疾病的强大保护,类似于目前市售的 YF 疫苗。