bioRxiv (Cold Spring Harbor Laboratory) · 2021 · 156 citations · 65 references
Life SciencesImmunologyInfectious DiseasesAdaptive ImmunityVaccine ImmunologyVaccinologyAdaptive Immune ModulationAdaptive Immune ResponsesAntigen RecognitionCell-mediated ImmunityHelper T Cell SubsetsImmune Response To VaccinationAdaptive Immune Repertoire DiversityAdaptive Immune RepertoiresAdaptive Immune Response VariationAdaptive Immune Responses To Viral InfectionCd8 Positive T Cell ResponsesCellular Immune Response AnalysisT-cell EpitopesT-cell Immunogenicity
The emergence of SARS-CoV-2 variants highlighted the need to better understand adaptive immune responses to this virus. It is important to address whether also CD4+ and CD8+ T cell responses are affected, because of the role they play in disease resolution and modulation of COVID-19 disease severity. Here we performed a comprehensive analysis of SARS-CoV-2-specific CD4+ and CD8+ T cell responses from COVID-19 convalescent subjects recognizing the ancestral strain, compared to variant lineages B.1.1.7, B.1.351, P.1, and CAL.20C as well as recipients of the Moderna (mRNA-1273) or Pfizer/BioNTech (BNT162b2) COVID-19 vaccines. Similarly, we demonstrate that the sequences of the vast majority of SARS-CoV-2 T cell epitopes are not affected by the mutations found in the variants analyzed. Overall, the results demonstrate that CD4+ and CD8+ T cell responses in convalescent COVID-19 subjects or COVID-19 mRNA vaccinees are not substantially affected by mutations found in the SARS-CoV-2 variants.
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Merryn Voysey, Sue Ann Costa Clemens, Shabir A. Madhi et al. · The Lancet · 2020 · 5K citations · Full text
Veterinary Medicine, Infectious Diseases, Preventive Medicine +17
Immunological memory to SARS-CoV-2 assessed for up to 8 months after infection
Jennifer M. Dan, José Mateus, Yu Kato et al. · Science · 2021 · 3K citations · Full text