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 in | Vaccines (Basel) Vol. 9; no. 8; p. 918 |
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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. |
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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.) |
Author_xml | – sequence: 1 givenname: Dorit surname: Fabricius fullname: Fabricius, Dorit – sequence: 2 givenname: Carolin orcidid: 0000-0001-8820-8479 surname: Ludwig fullname: Ludwig, Carolin – sequence: 3 givenname: Judith surname: Scholz fullname: Scholz, Judith – sequence: 4 givenname: Immanuel surname: Rode fullname: Rode, Immanuel – sequence: 5 givenname: Chrysanthi surname: Tsamadou fullname: Tsamadou, Chrysanthi – sequence: 6 givenname: Eva-Maria surname: Jacobsen fullname: Jacobsen, Eva-Maria – sequence: 7 givenname: Martina surname: Winkelmann fullname: Winkelmann, Martina – sequence: 8 givenname: Aline surname: Grempels fullname: Grempels, Aline – sequence: 9 givenname: Ramin surname: Lotfi fullname: Lotfi, Ramin – sequence: 10 givenname: Aleš orcidid: 0000-0001-5604-8378 surname: Janda fullname: Janda, Aleš – sequence: 11 givenname: Sixten surname: Körper fullname: Körper, Sixten – sequence: 12 givenname: Guido surname: Adler fullname: Adler, Guido – sequence: 13 givenname: Klaus-Michael surname: Debatin fullname: Debatin, Klaus-Michael – sequence: 14 givenname: Hubert surname: Schrezenmeier fullname: Schrezenmeier, Hubert – sequence: 15 givenname: Bernd orcidid: 0000-0002-8334-5244 surname: Jahrsdörfer fullname: Jahrsdörfer, Bernd |
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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 |
URI | https://www.proquest.com/docview/2565715209 https://www.proquest.com/docview/2566041708 https://pubmed.ncbi.nlm.nih.gov/PMC8402682 https://doaj.org/article/b34f0c5ef6774f098e7f53ae0cb15acf |
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