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Durable Humoral and Cellular Immune Responses Following Ad26.COV2.S Vaccination for COVID-19
Interim immunogenicity and efficacy data for the Ad26.COV2.S vaccine for COVID-19 have recently been reported(1–3). We describe here the 8-month durability of humoral and cellular immune responses in 20 individuals who received one or two doses of 5×10(10) vp or 10(11) vp Ad26.COV2.S and in 5 partic...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282116/ https://www.ncbi.nlm.nih.gov/pubmed/34268527 http://dx.doi.org/10.1101/2021.07.05.21259918 |
Sumario: | Interim immunogenicity and efficacy data for the Ad26.COV2.S vaccine for COVID-19 have recently been reported(1–3). We describe here the 8-month durability of humoral and cellular immune responses in 20 individuals who received one or two doses of 5×10(10) vp or 10(11) vp Ad26.COV2.S and in 5 participants who received placebo(2). We evaluated antibody and T cell responses on day 239, which was 8 months after the single-shot vaccine regimen (N=10) or 6 months after the two-shot vaccine regimen (N=10), although the present study was not powered to compare these regimens(3). We also report neutralizing antibody responses against the parental SARS-CoV-2 WA1/2020 strain as well as against the SARS-CoV-2 variants D614G, B.1.1.7 (alpha), B.1.617.1 (kappa), B.1.617.2 (delta), P.1 (gamma), B.1.429 (epsilon), and B.1.351 (beta). |
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