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10.1002/iid3.496

http://scihub22266oqcxt.onion/10.1002/iid3.496
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34314576!8427053!34314576
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suck abstract from ncbi


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pmid34314576      Immun+Inflamm+Dis 2021 ; 9 (4): 1452-1467
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  • SARS-CoV-2 spike glycoprotein-reactive T cells can be readily expanded from COVID-19 vaccinated donors #MMPMID34314576
  • Taborska P; Lastovicka J; Stakheev D; Strizova Z; Bartunkova J; Smrz D
  • Immun Inflamm Dis 2021[Dec]; 9 (4): 1452-1467 PMID34314576show ga
  • INTRODUCTION: The COVID-19 vaccine was designed to provide protection against infection by the severe respiratory coronavirus 2 (SARS-CoV-2) and coronavirus disease 2019 (COVID-19). However, the vaccine's efficacy can be compromised in patients with immunodeficiencies or the vaccine-induced immunoprotection suppressed by other comorbidity treatments, such as chemotherapy or immunotherapy. To enhance the protective role of the COVID-19 vaccine, we have investigated a combination of the COVID-19 vaccination with ex vivo enrichment and large-scale expansion of SARS-CoV-2 spike glycoprotein-reactive CD4(+) and CD8(+) T cells. METHODS: SARS-CoV-2-unexposed donors were vaccinated with two doses of the BNT162b2 SARS-CoV-2 vaccine. The peripheral blood mononuclear cells of the vaccinated donors were cell culture-enriched with T cells reactive to peptides derived from SARS-CoV-2 spike glycoprotein. The enriched cell cultures were large-scale expanded using the rapid expansion protocol (REP) and the peptide-reactive T cells were evaluated. RESULTS: We show that vaccination with the SARS-CoV-2 spike glycoprotein-based mRNA COVID-19 vaccine-induced humoral response against SARS-CoV-2 spike glycoprotein in all tested healthy SARS-CoV-2-unexposed donors. This humoral response was found to correlate with the ability of the donors' PBMCs to become enriched with SARS-CoV-2 spike glycoprotein-reactive CD4(+) and CD8(+) T cells. Using an 11-day REP, the enriched cell cultures were expanded nearly 1000-fold, and the proportions of the SARS-CoV-2 spike glycoprotein-reactive T cells increased. CONCLUSION: These findings show for the first time that the combination of the COVID-19 vaccination and ex vivo T cell large-scale expansion of SARS-CoV-2-reactive T cells could be a powerful tool for developing T cell-based adoptive cellular immunotherapy of COVID-19.
  • |*COVID-19 Vaccines[MESH]
  • |*COVID-19/immunology[MESH]
  • |Antibodies, Viral[MESH]
  • |BNT162 Vaccine[MESH]
  • |CD8-Positive T-Lymphocytes/*immunology[MESH]
  • |Glycoproteins[MESH]
  • |Humans[MESH]
  • |Leukocytes, Mononuclear[MESH]
  • |SARS-CoV-2[MESH]


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