Hertoghs Nina, Roels Sanne, Brückner Matthias, Sadoff Jerald, Banbury Barbara L, Akers Nicholas K, Howie Bryan, Robins Harlan S, van Roey Griet A, Tolboom Jeroen T B M, Rezelj Veronica V, Hendriks Jenny, Schuitemaker Hanneke, Stieh Daniel J, Le Gars Mathieu
Janssen Vaccines and Prevention, Leiden, the Netherlands.
Janssen Research and Development, Beerse, Belgium.
EBioMedicine. 2025 Jul;117:105809. doi: 10.1016/j.ebiom.2025.105809. Epub 2025 Jun 14.
While vaccine-induced SARS-CoV-2 antibodies provide partial protection against COVID-19, a significant question remains regarding the role of vaccine-induced T cells in combating COVID-19. The purpose of this study is to investigate whether signatures of the T-cell response contribute to protection against (severe) COVID-19.
T cell receptor (TCR) sequencing was conducted using pre-vaccination and 29 days post-vaccination PAXgene samples from 396 participants in the phase 3 efficacy trial, ENSEMBLE. The dataset consists of 198 individuals who developed breakthrough COVID-19 infections, including 23 severe cases, and an equal number of matched control subjects. Immunosequencing and subsequent computational analysis was performed to identify SARS-CoV-2 and Spike-specific TCRs to quantify SARS-CoV-2 specific T cell breadth, depth, clonal expansion, and a model test score that describes magnitude of cellular response compared to pre-pandemic controls.
Preliminary analyses demonstrated high concordance and correlation between functional T cell responses measured by a standard intracellular cytokine staining and TCR sequencing metrics. Furthermore, vaccine-elicited T cell responses correlated inversely with the risk of developing severe COVID-19, while no strong relation was observed with overall symptomatic COVID-19 risk. A multivariable analysis including neutralizing antibody data and TCR scores indicated that, in addition to humoural responses, T cell responses contribute to protection against severe COVID-19.
Our findings show that higher vaccine-elicited T cell responses are significantly correlated with decreased risk of severe COVID-19, but not with risk of any symptomatic COVID-19. These results represent a direct correlation between vaccine-elicited T cell responses and protection from severe COVID-19.
This work was fully funded by Janssen Vaccines & Prevention B.V. The samples were sourced from ENSEMBLE, which was partly funded by Biomedical Advanced Research and Development Authority (BARDA), under other transaction agreement HHSO100201700018C.
虽然疫苗诱导的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)抗体可提供针对2019冠状病毒病(COVID-19)的部分保护,但疫苗诱导的T细胞在对抗COVID-19中的作用仍存在重大疑问。本研究的目的是调查T细胞反应特征是否有助于预防(重症)COVID-19。
使用3期疗效试验ENSEMBLE中396名参与者接种疫苗前和接种疫苗后29天的PAXgene样本进行T细胞受体(TCR)测序。数据集包括198名发生突破性COVID-19感染的个体,其中包括23例重症病例,以及数量相等的匹配对照受试者。进行免疫测序及后续计算分析,以鉴定SARS-CoV-2和刺突蛋白特异性TCR,从而量化SARS-CoV-2特异性T细胞广度、深度、克隆扩增,以及一个描述与大流行前对照相比细胞反应强度的模型测试分数。
初步分析表明,通过标准细胞内细胞因子染色测量的功能性T细胞反应与TCR测序指标之间具有高度一致性和相关性。此外,疫苗诱导的T细胞反应与发生重症COVID-19的风险呈负相关,而与有症状COVID-19的总体风险未观察到强关联。一项包括中和抗体数据和TCR分数的多变量分析表明,除体液反应外,T细胞反应有助于预防重症COVID-19。
我们的研究结果表明,较高的疫苗诱导T细胞反应与重症COVID-19风险降低显著相关,但与任何有症状COVID-19的风险无关。这些结果表明疫苗诱导的T细胞反应与预防重症COVID-19之间存在直接关联。
本研究由杨森疫苗与预防有限公司全额资助。样本来自ENSEMBLE,该项目部分由生物医学高级研究与发展管理局(BARDA)根据其他交易协议HHSO100201700018C资助。