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Ahmed, Mohamed Ibraheem Mahmoud; Diepers, Paulina; Janke, Christian; Plank, Michael; Eser, Tabea M.; Rubio-Acero, Raquel; Fuchs, Anna; Baranov, Olga; Castelletti, Noemi; Kroidl, Inge; Olbrich, Laura; Bauer, Bernadette; Wang, Danni; Prelog, Martina; Liese, Johannes G.; Reinkemeyer, Christina; Hoelscher, Michael; Steininger, Philipp; Überla, Klaus; Wieser, Andreas; Geldmacher, Christof

Enhanced Spike-specific, but attenuated Nucleocapsid-specific T cell responses upon SARS-CoV-2 breakthrough versus non-breakthrough infections

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  • Media type: E-Article
  • Title: Enhanced Spike-specific, but attenuated Nucleocapsid-specific T cell responses upon SARS-CoV-2 breakthrough versus non-breakthrough infections
  • Contributor: Ahmed, Mohamed Ibraheem Mahmoud; Diepers, Paulina; Janke, Christian; Plank, Michael; Eser, Tabea M.; Rubio-Acero, Raquel; Fuchs, Anna; Baranov, Olga; Castelletti, Noemi; Kroidl, Inge; Olbrich, Laura; Bauer, Bernadette; Wang, Danni; Prelog, Martina; Liese, Johannes G.; Reinkemeyer, Christina; Hoelscher, Michael; Steininger, Philipp; Überla, Klaus; Wieser, Andreas; Geldmacher, Christof
  • imprint: Frontiers Media SA, 2022
  • Published in: Frontiers in Immunology
  • Language: Not determined
  • DOI: 10.3389/fimmu.2022.1026473
  • ISSN: 1664-3224
  • Origination:
  • Footnote:
  • Description: <jats:p>SARS-CoV-2 vaccine breakthrough infections frequently occurred even before the emergence of Omicron variants. Yet, relatively little is known about the impact of vaccination on SARS-CoV-2-specific T cell and antibody response dynamics upon breakthrough infection. We have therefore studied the dynamics of CD4 and CD8 T cells targeting the vaccine-encoded Spike and the non-encoded Nucleocapsid antigens during breakthrough infections (BTI, n=24) and in unvaccinated control infections (non-BTI, n=30). Subjects with vaccine breakthrough infection had significantly higher CD4 and CD8 T cell responses targeting the vaccine-encoded Spike during the first and third/fourth week after PCR diagnosis compared to non-vaccinated controls, respectively. In contrast, CD4 T cells targeting the non-vaccine encoded Nucleocapsid antigen were of significantly lower magnitude in BTI as compared to non-BTI. Hence, previous vaccination was linked to enhanced T cell responses targeting the vaccine-encoded Spike antigen, while responses against the non-vaccine encoded Nucleocapsid antigen were significantly attenuated.</jats:p>
  • Access State: Open Access