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首页> 外文期刊>Vaccine >Haemagglutinin stability was not the primary cause of the reduced effectiveness of live attenuated influenza vaccine against A/H1N1pdm09 viruses in the 2013-2014 and 2015-2016 seasons
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Haemagglutinin stability was not the primary cause of the reduced effectiveness of live attenuated influenza vaccine against A/H1N1pdm09 viruses in the 2013-2014 and 2015-2016 seasons

机译:Haemagglutinin稳定性不是在2013 - 2014年和2015-2016赛季中针对A / H1N1PDM09病毒减少活化流感疫苗的减少效果的主要原因

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During the 2013-2014 influenza season, the quadrivalent live attenuated influenza vaccine (QLAIV), had lower than expected vaccine effectiveness (VE) against circulating A/H1N1pdm09 viruses in the USA. The underlying reason proposed for this was that the A/H1N1pdm09 vaccine strain, A/California/07/2009 (A/CA09), had a thermally unstable haemagglutinin (HA) protein. Consequently, a new A/H1N1pdm09 candidate strain, A/Bolivia/559/2013 (A/BOL13), was developed for inclusion in the 2015-2016 QLAIV. A key parameter for selection of A/BOL13 was its more thermostable HA phenotype compared with A/CA09. During the 2015-2016 season, QLAIV containing A/BOL13 was found in some studies to have improved, but still with suboptimal, VE against circulating A/H1N1pdm09 viruses and was not recommended for use by the CDC in the US market in the 2016-2017 influenza season. This suggested that improved HA thermostability had not entirely resolved the reduced VE observed. One hypothesis for this was that, by improving thermostability, the A/BOL13 HA protein had been over-stabilised, compromising its activation at the low endosomal pH required for successful viral entry. Here we demonstrate that, while the A/BOL13 HA protein is more stable than that of A/CA09, its thermal and pH stability were comparable with historically efficacious LAIV strains, suggesting that the HA had not been over-stabilised. Furthermore, studies simulating potential heat exposure during distribution by exposing QLAIV nasal sprayers to 33 degrees C for 4 h showed that, while remaining within product specification, A/CA09 viral potency was statistically decreased after 12 weeks at 2-8 degrees C. These data suggest that although unfavourable HA protein stability may have contributed to the reduced VE of A/CA09 in 2013-2014, it was unlikely to have affected A/BOL13 in 2015-2016. We conclude that HA stability was not the primary cause of the reduced effectiveness of LAIV against A/H1N1pdm09 viruses in the 2013-2014 and 2015-2016 seasons. (C) 2019 The Authors. Published by Elsevier Ltd.
机译:在2013-2014流感季节期间,四轮脑活病毒病毒的流感疫苗(QLAIV)较低的疫苗有效性(VE)对美国的循环A / H1N1PDM09病毒。提出的潜在原因是A / H1N1PDM09疫苗菌株,A / CALIFORNIA / 07/2009(A / CAO 9)具有热不稳定的血凝素(HA)蛋白。因此,开发了一种新的A / H1N1PDM09候选菌株,A / Bolivia / 559/2013(A / BOL13),用于纳入2015-2016 QLAIV。与A / CA09相比,选择A / BOL13的关键参数是其更热稳定的HA表型。在2015-2016赛季期间,在一些研究中发现了含有A / BOL13的QLAIV,以改善,但仍然与次优,ve反对循环A / H1N1PDM09病毒,并未建议在2016年美国市场中的CDC使用。 2017年流感季节。这表明改善了HA热稳定性并不完全解决观察到的减少。一个假设是,通过提高热稳定性,A / BOL13 HA蛋白已过度稳定,损害其在成功病毒进入所需的低内体pH下的活化。在这里,我们证明,虽然A / BOL13 HA蛋白比A / CA09更稳定,但其热和pH稳定性与历史上有效的LAIV菌株相当,表明HA没有过度稳定。此外,通过将QLAIV鼻喷雾器暴露于33℃的分布期间,在4小时内进行分布模拟潜在热暴露的研究表明,在产品规格内保持在剩余的同时,在2-8℃下在12周后统计学上降低。这些数据建议,尽管不利的HA蛋白质稳定性可能导致2013 - 2014年的A / CA09的减少,但在2015-2016中不太可能影响A / BOL13。我们得出结论,HA稳定性不是LaIV对2013 - 2014年和2015-2016赛季A / H1N1PDM09病毒减少的主要原因。 (c)2019年作者。 elsevier有限公司出版

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