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mRNA Vaccines Enhance Neutralizing Immunity against SARS-CoV-2 Variants in Convalescent and ChAdOx1-Primed Subjects.
Fabricius, Dorit; Ludwig, Carolin; Scholz, Judith; Rode, Immanuel; Tsamadou, Chrysanthi; Jacobsen, Eva-Maria; Winkelmann, Martina; Grempels, Aline; Lotfi, Ramin; Janda, Ales; Körper, Sixten; Adler, Guido; Debatin, Klaus-Michael; Schrezenmeier, Hubert; Jahrsdörfer, Bernd.
  • Fabricius D; Division of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
  • Ludwig C; Division of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
  • Scholz J; Division of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
  • Rode I; Division of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
  • Tsamadou C; Division of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
  • Jacobsen EM; Division of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
  • Winkelmann M; Division of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
  • Grempels A; Division of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
  • Lotfi R; Division of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
  • Janda A; Division of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
  • Körper S; Division of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
  • Adler G; Division of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
  • Debatin KM; Division of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
  • Schrezenmeier H; Division of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
  • Jahrsdörfer B; Division of Immune Cell Therapeutics, Institute of Clinical Transfusion Medicine and Immunogenetics, Helmholtzstrasse 10, 89081 Ulm, Germany.
Vaccines (Basel) ; 9(8)2021 Aug 18.
Article in English | MEDLINE | ID: covidwho-1360834
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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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines / Variants Language: English Year: 2021 Document Type: Article Affiliation country: Vaccines9080918

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines / Variants Language: English Year: 2021 Document Type: Article Affiliation country: Vaccines9080918