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A bivalent SARS-CoV-2 monoclonal antibody combination does not affect the immunogenicity of a vector-based COVID-19 vaccine in macaques.

Joseph P NkololaJingyou YuHuahua WanAiquan ChangKatherine A McMahanTochi AniokeCatherine Jacob-DolanOlivia PowersTianyi YeAbishek ChandrashekarDaniel SellersJulia BarrettYueh-Ming LooMark T EsserRobert H CarnahanJames E CroweDan H Barouch
Published in: Science translational medicine (2022)
Human monoclonal antibodies (mAbs) that target the spike glycoprotein of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) offer a promising approach for the prevention and treatment of coronavirus disease 2019 (COVID-19). Given suboptimal global vaccination rates, waning immunity in vaccinated individuals, and the emergence of SARS-CoV-2 variants of concern, the use of mAbs for COVID-19 prevention may increase and may need to be administered together with vaccines in certain settings. However, it is unknown whether administration of mAbs will affect the immunogenicity of SARS-CoV-2 vaccines. Using an adenovirus vector-based SARS-CoV-2 vaccine, we show that simultaneous administration of the vaccine with SARS-CoV-2 mAbs does not diminish vaccine-induced humoral or cellular immunity in cynomolgus macaques. These results suggest that SARS-CoV-2 mAbs and viral vector-based SARS-CoV-2 vaccines can be administered together without loss of potency of either product. Additional studies will be required to evaluate coadministration of mAbs with other vaccine platforms.
Keyphrases
  • sars cov
  • respiratory syndrome coronavirus
  • coronavirus disease
  • monoclonal antibody
  • endothelial cells
  • oxidative stress
  • gene expression
  • dna methylation
  • smoking cessation
  • high glucose
  • replacement therapy