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模型表明,多次免疫接种或感染将揭示更新新冠病毒疫苗的益处。

Modeling suggests that multiple immunizations or infections will reveal the benefits of updating SARS-CoV-2 vaccines.

作者信息

Desikan Rajat, Linderman Susanne L, Davis Carl, Zarnitsyna Veronika, Ahmed Hasan, Antia Rustom

机构信息

Clinical Pharmacology Modeling & Simulation, GlaxoSmithKline (GSK), Gunnels Wood Rd, Stevenage, Hertfordshire, SG1 2NY, United Kingdom.

These authors contributed equally.

出版信息

bioRxiv. 2022 May 23:2022.05.21.492928. doi: 10.1101/2022.05.21.492928.

Abstract

When should vaccines to evolving pathogens such as SARS-CoV-2 be updated? Our computational models address this focusing on updating SARS-CoV-2 vaccines to the currently circulating Omicron variant. Current studies typically compare the antibody titers to the new variant following a single dose of the original-vaccine versus the updated-vaccine in previously immunized individuals. These studies find that the updated-vaccine does not induce higher titers to the vaccine-variant compared with the original-vaccine, suggesting that updating may not be needed. Our models recapitulate this observation but suggest that vaccination with the updated-vaccine generates qualitatively different humoral immunity, a small fraction of which is specific for unique epitopes to the new variant. Our simulations suggest that these new variant-specific responses could dominate following subsequent vaccination or infection with either the currently circulating or future variants. We suggest a two-dose strategy for determining if the vaccine needs updating and for vaccinating high-risk individuals.

摘要

对于像严重急性呼吸综合征冠状病毒2(SARS-CoV-2)这样不断演变的病原体,疫苗应在何时更新?我们的计算模型聚焦于将SARS-CoV-2疫苗更新为当前流行的奥密克戎变体来解决这一问题。当前的研究通常比较既往免疫个体接种一剂原始疫苗与更新疫苗后针对新变体的抗体滴度。这些研究发现,与原始疫苗相比,更新疫苗不会诱导产生更高的针对疫苗变体的滴度,这表明可能不需要进行更新。我们的模型重现了这一观察结果,但表明接种更新疫苗会产生质的不同的体液免疫,其中一小部分针对新变体的独特表位具有特异性。我们的模拟表明,在随后接种疫苗或感染当前流行或未来的变体后,这些针对新变体的特异性反应可能占主导。我们建议采用两剂策略来确定疫苗是否需要更新以及为高危个体接种疫苗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/558c/9164442/baa62831b6cd/nihpp-2022.05.21.492928v1-f0001.jpg

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