4.8 Article

T cell and antibody responses induced by a single dose of ChAdOx1 nCoV-19 (AZD1222) vaccine in a phase 1/2 clinical trial

期刊

NATURE MEDICINE
卷 27, 期 2, 页码 270-+

出版社

NATURE PORTFOLIO
DOI: 10.1038/s41591-020-01194-5

关键词

-

资金

  1. UK Research and Innovation [MC_PC_19055]
  2. Engineering and Physical Sciences Research Council [EP/R013756/1]
  3. Coalition for Epidemic Preparedness Innovations (CEPI)
  4. National Institute for Health Research (NIHR)
  5. NIHR Oxford Biomedical Research Centre
  6. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior, Brazil [001]
  7. U.S. National Institute of Allergy and Infectious Diseases Centers of Excellence for Influenza Research and Surveillance [HHSN272201400008C]
  8. Huo Family Foundation
  9. Medical Sciences Division
  10. Versus Arthritis [21509]
  11. Wellcome MSD ISSF [BRD00010]
  12. Kennedy Trust for Rheumatology Research
  13. Chinese Academy of Medical Sciences Innovation Fund for Medical Science, China [2018-I2M-2-002]
  14. Nuffield Department of Medicine
  15. Department of Paediatrics
  16. Oxford Immunology Network COVID Consortium, Clinical Trials Research Governance
  17. Public Affairs Directorate
  18. Clinical Biomanufacturing Facility
  19. Oxford University Hospitals NHS Foundation Trust
  20. Oxford Health NHS Foundation Trust
  21. AstraZeneca
  22. EPSRC [EP/R013756/1] Funding Source: UKRI
  23. MRC [G0600520, MC_PC_19058, G1001046, MR/T001151/1, MC_UU_00008/11, MC_PC_19055, MR/L018942/1] Funding Source: UKRI

向作者/读者索取更多资源

A single dose of the ChAdOx1 nCoV-19 vaccine can induce favorable immune responses that may help control or prevent SARS-CoV-2 infection.
A single dose of the ChAdOx1 nCoV-19 vaccine elicits antibodies and cytokine-producing T cells that might help control or prevent SARS-CoV-2 infection. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of Coronavirus Disease 2019 (COVID-19), has caused a global pandemic, and safe, effective vaccines are urgently needed(1). Strong, Th1-skewed T cell responses can drive protective humoral and cell-mediated immune responses(2) and might reduce the potential for disease enhancement(3). Cytotoxic T cells clear virus-infected host cells and contribute to control of infection(4). Studies of patients infected with SARS-CoV-2 have suggested a protective role for both humoral and cell-mediated immune responses in recovery from COVID-19 (refs. (5,6)). ChAdOx1 nCoV-19 (AZD1222) is a candidate SARS-CoV-2 vaccine comprising a replication-deficient simian adenovirus expressing full-length SARS-CoV-2 spike protein. We recently reported preliminary safety and immunogenicity data from a phase 1/2 trial of the ChAdOx1 nCoV-19 vaccine (NCT04400838)(7) given as either a one- or two-dose regimen. The vaccine was tolerated, with induction of neutralizing antibodies and antigen-specific T cells against the SARS-CoV-2 spike protein. Here we describe, in detail, exploratory analyses of the immune responses in adults, aged 18-55 years, up to 8 weeks after vaccination with a single dose of ChAdOx1 nCoV-19 in this trial, demonstrating an induction of a Th1-biased response characterized by interferon-gamma and tumor necrosis factor-alpha cytokine secretion by CD4(+) T cells and antibody production predominantly of IgG1 and IgG3 subclasses. CD8(+) T cells, of monofunctional, polyfunctional and cytotoxic phenotypes, were also induced. Taken together, these results suggest a favorable immune profile induced by ChAdOx1 nCoV-19 vaccine, supporting the progression of this vaccine candidate to ongoing phase 2/3 trials to assess vaccine efficacy.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据