Longitudinal analysis of immune responses to SARS-CoV-2 recombinant vaccine S-268019-b in phase 1/2 prime-boost study.

IF 5.9 2区 医学 Q1 IMMUNOLOGY Frontiers in Immunology Pub Date : 2025-03-05 eCollection Date: 2025-01-01 DOI:10.3389/fimmu.2025.1550279
Masaya Fujitani, Xiuyuan Lu, Ryo Shinnakasu, Takeshi Inoue, Yujiro Kidani, Naomi M Seki, Satoru Ishida, Shungo Mitsuki, Takeshi Ishihara, Miwa Aoki, Akio Suzuki, Koji Takahashi, Masahiro Takayama, Takeshi Ota, Satoshi Iwata, Risa Yokokawa Shibata, Takuhiro Sonoyama, Mari Ariyasu, Ayumi Kitano, Tommy Terooatea, Jordan Kelly Villa, Kazuo Yamashita, Sho Yamasaki, Tomohiro Kurosaki, Shinya Omoto
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Abstract

Background: The durability of vaccine-induced immune memory to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is crucial for preventing infection, especially severe disease.

Methods: This follow-up report from a phase 1/2 study of S-268019-b (a recombinant spike protein vaccine) after homologous booster vaccination confirms its long-term safety, tolerability, and immunogenicity.

Results: Booster vaccination with S-268019-b resulted in an enhancement of serum neutralizing antibody (NAb) titers and a broad range of viral neutralization. Single-cell immune profiling revealed persistent and mature antigen-specific memory B cells and T follicular helper cells, with increased B-cell receptor diversity. The expansion of B- and T-cell repertoires and presence of cross-reactive NAbs targeting conserved epitopes within the receptor-binding domain following a booster accounted for the broad-spectrum neutralizing activity.

Conclusion: These findings highlight the potential of S-268019-b to provide broad and robust protection against a range of SARS-CoV-2 variants, addressing a critical challenge in the ongoing fight against coronavirus disease 2019 (COVID-19).

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SARS-CoV-2重组疫苗S-268019-b在1/2期预强化研究中的免疫应答纵向分析
背景:疫苗诱导的对严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)的免疫记忆的持久性对于预防感染,特别是严重疾病的感染至关重要。方法:S-268019-b(一种重组刺突蛋白疫苗)同源强化疫苗接种后的1/2期随访报告证实了其长期安全性、耐受性和免疫原性。结果:S-268019-b加强疫苗接种可提高血清中和抗体(NAb)滴度和广泛的病毒中和作用。单细胞免疫谱显示持久和成熟的抗原特异性记忆B细胞和T滤泡辅助细胞,B细胞受体多样性增加。B细胞和t细胞库的扩增以及在受体结合区域内靶向保守表位的交叉反应性nab的存在解释了广谱中和活性。结论:这些发现突出了S-268019-b的潜力,可以针对一系列SARS-CoV-2变体提供广泛而强大的保护,从而解决当前抗击2019冠状病毒病(COVID-19)的关键挑战。
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来源期刊
CiteScore
9.80
自引率
11.00%
发文量
7153
审稿时长
14 weeks
期刊介绍: Frontiers in Immunology is a leading journal in its field, publishing rigorously peer-reviewed research across basic, translational and clinical immunology. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Immunology is the official Journal of the International Union of Immunological Societies (IUIS). Encompassing the entire field of Immunology, this journal welcomes papers that investigate basic mechanisms of immune system development and function, with a particular emphasis given to the description of the clinical and immunological phenotype of human immune disorders, and on the definition of their molecular basis.
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