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XBB.1.5 单价 mRNA 疫苗加强针可诱导针对 XBB 亚谱系和 JN.1 的强大中和抗体。

XBB.1.5 monovalent mRNA vaccine booster elicits robust neutralizing antibodies against XBB subvariants and JN.1.

机构信息

Aaron Diamond AIDS Research Center, Columbia University Vagelos College of Physicians and Surgeons, New York, NY 10032, USA.

Aaron Diamond AIDS Research Center, Columbia University Vagelos College of Physicians and Surgeons, New York, NY 10032, USA; Division of Infectious Diseases, Department of Medicine, Columbia University Vagelos College of Physicians and Surgeons, New York, NY 10032, USA.

出版信息

Cell Host Microbe. 2024 Mar 13;32(3):315-321.e3. doi: 10.1016/j.chom.2024.01.014. Epub 2024 Feb 19.

Abstract

COVID-19 vaccines have recently been updated to specifically encode or contain the spike protein of the SARS-CoV-2 XBB.1.5 subvariant, but their immunogenicity in humans has yet to be fully evaluated and reported, particularly against emergent viruses that are rapidly expanding. We now report that administration of an updated monovalent mRNA vaccine booster (XBB.1.5 MV) to previously uninfected individuals boosted serum virus-neutralizing antibodies significantly against not only XBB.1.5 (27.0-fold increase) and EG.5.1 (27.6-fold increase) but also key emerging viruses such as HV.1, HK.3, JD.1.1, and JN.1 (13.3- to 27.4-fold increase). Individuals previously infected by an Omicron subvariant had the highest overall serum neutralizing titers (ID 1,504-22,978) against all viral variants tested. While immunological imprinting was still evident with the updated vaccines, it was not nearly as severe as observed with the previously authorized bivalent BA.5 vaccine. Our findings strongly support the official recommendation to widely apply the updated COVID-19 vaccines.

摘要

COVID-19 疫苗最近已更新为专门编码或包含 SARS-CoV-2 XBB.1.5 亚变体的刺突蛋白,但它们在人类中的免疫原性尚未得到充分评估和报告,特别是针对迅速扩张的新兴病毒。我们现在报告,对以前未感染的个体施用更新的单价 mRNA 疫苗加强针(XBB.1.5 MV),不仅显著增强了针对 XBB.1.5(27.0 倍增加)和 EG.5.1(27.6 倍增加)的血清病毒中和抗体,而且还增强了针对 HV.1、HK.3、JD.1.1 和 JN.1 等关键新兴病毒的抗体(13.3-27.4 倍增加)。以前被奥密克戎亚变体感染的个体对所有测试的病毒变体具有最高的总体血清中和滴度(ID 1,504-22978)。虽然更新后的疫苗仍存在免疫印迹现象,但与之前授权的二价 BA.5 疫苗相比,其严重程度要低得多。我们的研究结果强烈支持广泛应用更新的 COVID-19 疫苗的官方建议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0567/10957340/4dd3bb7caae4/fx1.jpg

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