4.6 Review

Immunogenicity and efficacy of Ad26.COV2.S: An adenoviral vector-based COVID-19 vaccine

期刊

IMMUNOLOGICAL REVIEWS
卷 310, 期 1, 页码 47-60

出版社

WILEY
DOI: 10.1111/imr.13088

关键词

COVID-19; efficacy; immunogenicity; SARS-CoV-2; vaccination; vaccine

资金

  1. Janssen Vaccines & Prevention B.V.
  2. National Institutes of Health
  3. National Institute of Allergy and Infectious Diseases
  4. Biomedical Advanced Research and Development Authority

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This review discusses the immunogenicity and efficacy of Ad26.COV2.S vaccine as a primary vaccination and as a booster vaccination against COVID-19. The vaccine elicits broad humoral and cellular immune responses, providing protection against SARS-CoV-2 infection and severe/critical COVID-19, including against emerging variants. The humoral immune responses are durable and can be significantly enhanced when Ad26.COV2.S is used as a booster in individuals who received mRNA vaccines.
Since its emergence in late 2019, the coronavirus disease 2019 (COVID-19) pandemic has caused substantial morbidity and mortality. Despite the availability of efficacious vaccines, new variants with reduced sensitivity to vaccine-induced protection are a troubling new reality. The Ad26.COV2.S vaccine is a recombinant, replication-incompetent human adenovirus type 26 vector encoding a full-length, membrane-bound severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike protein in a prefusion-stabilized conformation. This review discusses the immunogenicity and efficacy of Ad26.COV2.S as a single-dose primary vaccination and as a homologous or heterologous booster vaccination. Ad26.COV2.S elicits broad humoral and cellular immune responses, which are associated with protective efficacy/effectiveness against SARS-CoV-2 infection, moderate to severe/critical COVID-19, and COVID-19-related hospitalization and death, including against emerging SARS-CoV-2 variants. The humoral immune responses elicited by Ad26.COV2.S vaccination are durable, continue to increase for at least 2-3 months postvaccination, and involve a range of functional antibodies. Ad26.COV2.S given as a heterologous booster to mRNA vaccine-primed individuals markedly increases humoral and cellular immune responses. The use of Ad26.COV2.S as primary vaccination and as part of booster regimens is supporting the ongoing efforts to control and mitigate the COVID-19 pandemic.

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