mRNA Vaccines Enhance Neutralizing Immunity against SARS-CoV-2 Variants in Convalescent and ChAdOx1-Primed Subjects

To identify the most efficient methods of immunological protection against SARS-CoV-2, including the currently most widespread variants of concern (VOCs)—B.1.1.7, B.1.351 and P.1—a simultaneous side-by-side-comparison of available vaccination regimes is required. In this observational cohort study,...

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Published inVaccines (Basel) Vol. 9; no. 8; p. 918
Main Authors Fabricius, Dorit, Ludwig, Carolin, Scholz, Judith, Rode, Immanuel, Tsamadou, Chrysanthi, Jacobsen, Eva-Maria, Winkelmann, Martina, Grempels, Aline, Lotfi, Ramin, Janda, Aleš, Körper, Sixten, Adler, Guido, Debatin, Klaus-Michael, Schrezenmeier, Hubert, Jahrsdörfer, Bernd
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Published Basel MDPI AG 18.08.2021
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Abstract To identify the most efficient methods of immunological protection against SARS-CoV-2, including the currently most widespread variants of concern (VOCs)—B.1.1.7, B.1.351 and P.1—a simultaneous side-by-side-comparison of available vaccination regimes is required. In this observational cohort study, we compared immunological responses in 144 individuals vaccinated with the mRNA vaccines BNT162b2 or mRNA-1273 and the vector vaccine ChAdOx1-nCoV-19, either alone, in combination, or in the context of COVID-19-convalescence. Unvaccinated COVID-19-convalescent subjects served as a reference. We found that cellular and serological immune responses, including neutralizing capacity against VOCs, were significantly stronger with mRNA vaccines as compared with COVID-19-convalescent individuals or vaccinated individuals receiving the vector vaccine ChAdOx1-nCoV-19. Booster immunizations with mRNA vaccines triggered strong and broadly neutralizing antibody and IFN-γ responses in 100% of vaccinated individuals investigated. This effect was particularly strong in COVID-19-convalescent and ChAdOx1-nCoV-19-primed individuals, who were characterized by comparably moderate cellular and neutralizing antibody responses before mRNA vaccine booster. Heterologous vaccination regimes and convalescent booster regimes using mRNA vaccines may allow enhanced protection against SARS-CoV-2, including current VOCs. Furthermore, such regimes may facilitate rapid (re-)qualification of convalescent plasma donors with high titers of broadly neutralizing antibodies.
AbstractList To identify the most efficient methods of immunological protection against SARS-CoV-2, including the currently most widespread variants of concern (VOCs)-B.1.1.7, B.1.351 and P.1-a simultaneous side-by-side-comparison of available vaccination regimes is required. In this observational cohort study, we compared immunological responses in 144 individuals vaccinated with the mRNA vaccines BNT162b2 or mRNA-1273 and the vector vaccine ChAdOx1-nCoV-19, either alone, in combination, or in the context of COVID-19-convalescence. Unvaccinated COVID-19-convalescent subjects served as a reference. We found that cellular and serological immune responses, including neutralizing capacity against VOCs, were significantly stronger with mRNA vaccines as compared with COVID-19-convalescent individuals or vaccinated individuals receiving the vector vaccine ChAdOx1-nCoV-19. Booster immunizations with mRNA vaccines triggered strong and broadly neutralizing antibody and IFN-γ responses in 100% of vaccinated individuals investigated. This effect was particularly strong in COVID-19-convalescent and ChAdOx1-nCoV-19-primed individuals, who were characterized by comparably moderate cellular and neutralizing antibody responses before mRNA vaccine booster. Heterologous vaccination regimes and convalescent booster regimes using mRNA vaccines may allow enhanced protection against SARS-CoV-2, including current VOCs. Furthermore, such regimes may facilitate rapid (re-)qualification of convalescent plasma donors with high titers of broadly neutralizing antibodies.To identify the most efficient methods of immunological protection against SARS-CoV-2, including the currently most widespread variants of concern (VOCs)-B.1.1.7, B.1.351 and P.1-a simultaneous side-by-side-comparison of available vaccination regimes is required. In this observational cohort study, we compared immunological responses in 144 individuals vaccinated with the mRNA vaccines BNT162b2 or mRNA-1273 and the vector vaccine ChAdOx1-nCoV-19, either alone, in combination, or in the context of COVID-19-convalescence. Unvaccinated COVID-19-convalescent subjects served as a reference. We found that cellular and serological immune responses, including neutralizing capacity against VOCs, were significantly stronger with mRNA vaccines as compared with COVID-19-convalescent individuals or vaccinated individuals receiving the vector vaccine ChAdOx1-nCoV-19. Booster immunizations with mRNA vaccines triggered strong and broadly neutralizing antibody and IFN-γ responses in 100% of vaccinated individuals investigated. This effect was particularly strong in COVID-19-convalescent and ChAdOx1-nCoV-19-primed individuals, who were characterized by comparably moderate cellular and neutralizing antibody responses before mRNA vaccine booster. Heterologous vaccination regimes and convalescent booster regimes using mRNA vaccines may allow enhanced protection against SARS-CoV-2, including current VOCs. Furthermore, such regimes may facilitate rapid (re-)qualification of convalescent plasma donors with high titers of broadly neutralizing antibodies.
To identify the most efficient methods of immunological protection against SARS-CoV-2, including the currently most widespread variants of concern (VOCs)—B.1.1.7, B.1.351 and P.1—a simultaneous side-by-side-comparison of available vaccination regimes is required. In this observational cohort study, we compared immunological responses in 144 individuals vaccinated with the mRNA vaccines BNT162b2 or mRNA-1273 and the vector vaccine ChAdOx1-nCoV-19, either alone, in combination, or in the context of COVID-19-convalescence. Unvaccinated COVID-19-convalescent subjects served as a reference. We found that cellular and serological immune responses, including neutralizing capacity against VOCs, were significantly stronger with mRNA vaccines as compared with COVID-19-convalescent individuals or vaccinated individuals receiving the vector vaccine ChAdOx1-nCoV-19. Booster immunizations with mRNA vaccines triggered strong and broadly neutralizing antibody and IFN-γ responses in 100% of vaccinated individuals investigated. This effect was particularly strong in COVID-19-convalescent and ChAdOx1-nCoV-19-primed individuals, who were characterized by comparably moderate cellular and neutralizing antibody responses before mRNA vaccine booster. Heterologous vaccination regimes and convalescent booster regimes using mRNA vaccines may allow enhanced protection against SARS-CoV-2, including current VOCs. Furthermore, such regimes may facilitate rapid (re-)qualification of convalescent plasma donors with high titers of broadly neutralizing antibodies.
Author Tsamadou, Chrysanthi
Jacobsen, Eva-Maria
Adler, Guido
Winkelmann, Martina
Grempels, Aline
Jahrsdörfer, Bernd
Ludwig, Carolin
Janda, Aleš
Schrezenmeier, Hubert
Rode, Immanuel
Lotfi, Ramin
Körper, Sixten
Fabricius, Dorit
Debatin, Klaus-Michael
Scholz, Judith
AuthorAffiliation Division of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany; dorit.fabricius@uni-ulm.de (D.F.); c.ludwig@blutspende.de (C.L.); judith.scholz@uni-ulm.de (J.S.); i.rode@blutspende.de (I.R.); c.tsamadou@blutspende.de (C.T.); eva-maria.jacobsen@uni-ulm.de (E.-M.J.); m.winkelmann@blutspend.de (M.W.); a.grempels@blutspende.de (A.G.); r.lotfi@blutspende.de (R.L.); ales.janda@uniklinik-ulm.de (A.J.); s.koerper@blutspende.de (S.K.); guidoadler46@gmail.com (G.A.); klaus-Michael.Debatin@uniklinik-ulm.de (K.-M.D.); h.schrezenmeier@blutspende.de (H.S.)
AuthorAffiliation_xml – name: Division of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany; dorit.fabricius@uni-ulm.de (D.F.); c.ludwig@blutspende.de (C.L.); judith.scholz@uni-ulm.de (J.S.); i.rode@blutspende.de (I.R.); c.tsamadou@blutspende.de (C.T.); eva-maria.jacobsen@uni-ulm.de (E.-M.J.); m.winkelmann@blutspend.de (M.W.); a.grempels@blutspende.de (A.G.); r.lotfi@blutspende.de (R.L.); ales.janda@uniklinik-ulm.de (A.J.); s.koerper@blutspende.de (S.K.); guidoadler46@gmail.com (G.A.); klaus-Michael.Debatin@uniklinik-ulm.de (K.-M.D.); h.schrezenmeier@blutspende.de (H.S.)
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Snippet To identify the most efficient methods of immunological protection against SARS-CoV-2, including the currently most widespread variants of concern...
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SubjectTerms Antibodies
Antigens
Convalescence
Coronaviruses
COVID-19
COVID-19 vaccines
Cryopreservation
Enzymes
heterologous vaccination regimes using mRNA vaccines may allow enhanced protection against SARS-CoV-2, including current VOCs
Immune response
Immunology
mRNA
mRNA vaccines
Neutralizing
Observational studies
Proteins
RNA vaccines may facilitate rapid (re-) qualification of convalescent plasma donors with high titers of broadly neutralizing antibodies
Serology
Severe acute respiratory syndrome coronavirus 2
Statistical analysis
Vaccines
γ-Interferon
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Title mRNA Vaccines Enhance Neutralizing Immunity against SARS-CoV-2 Variants in Convalescent and ChAdOx1-Primed Subjects
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Volume 9
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