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Immunogenicity of heterologous inactivated and adenoviral-vectored COVID-19 vaccine: Real-world data. | LitMetric

AI Article Synopsis

  • * Results showed that the mixed vaccine group produced significantly higher levels of anti-RBD IgG compared to those who received two doses of the same vaccine (p < 0.001).
  • * The heterologous regimen demonstrated better neutralizing antibody activity against both the original Wuhan strain and various concerning variants, suggesting it could be a viable alternative during vaccine shortages.

Article Abstract

Limited data are available on the responses to heterologous vaccine regimens for SARS-CoV-2, especially among countries using inactivated and adenoviral-vectored vaccines. A total of 77 participants who received heterologous inactivated COVID-19 vaccine (CoronaVac) and adenoviral-vectored vaccine (AZD1222) were enrolled in our study. There were two comparison groups vaccinated with the homologous CoronaVac (N = 79) and AZD1222 (N = 78) regimen. All sera samples were tested for anti-receptor-binding-domain IgG (anti-RBD IgG) using a chemiluminescent microparticle immunoassay (CMIA). The neutralizing activity in a subset of serum samples was tested against the original Wuhan strain and variants of concern, B.1.1.7, B.1.617.2 and B.1.351, using an enzyme-linked immunosorbent assay (ELISA)-based surrogate virus neutralization test (sVNT). The heterologous CoronaVac/AZD1222 vaccine induced higher levels of anti-RBD IgG than that of two-dose homologous CoronaVac or AZD1222 vaccines (p < 0.001). Sera samples of the CoronaVac/AZD1222 vaccine recipients elicited higher neutralizing antibody activity against the original Wuhan and all variants of concern than in the recipients of the two-dose CoronaVac. The heterologous CoronaVac followed by AZD1222 is an alternative regimen to combat with the SARS-CoV-2 variants in case of vaccine shortage with improved immunogenicity compared to the homologous CoronaVac regimen.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9013645PMC
http://dx.doi.org/10.1016/j.vaccine.2022.04.043DOI Listing

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