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10.1111/tid.13602

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suck abstract from ncbi


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pmid33728702      Transpl+Infect+Dis 2021 ; 23 (4): e13602
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  • Adoptive transfer of ex vivo expanded SARS-CoV-2-specific cytotoxic lymphocytes: A viable strategy for COVID-19 immunosuppressed patients? #MMPMID33728702
  • Guerreiro M; Aguilar-Gallardo C; Montoro J; Frances-Gomez C; Latorre V; Luna I; Planelles D; Carrasco MP; Gomez MD; Gonzalez-Barbera EM; Aguado C; Sempere A; Solves P; Gomez-Segui I; Balaguer-Rosello A; Louro A; Perla A; Larrea L; Sanz J; Arbona C; de la Rubia J; Geller R; Sanz MA; Sanz G; Luis Pinana J
  • Transpl Infect Dis 2021[Aug]; 23 (4): e13602 PMID33728702show ga
  • Cellular and humoral response to acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections is on focus of research. We evaluate herein the feasibility of expanding virus-specific T cells (VST) against SARS-CoV-2 ex vivo through a standard protocol proven effective for other viruses. The experiment was performed in three different donors' scenarios: (a) SARS-CoV-2 asymptomatic infection/negative serology, (b) SARS-CoV-2 symptomatic infection/positive serology, and (c) no history of SARS-CoV-2 infection/negative serology. We were able to obtain an expanded VST product from donors 1 and 2 (1.6x and 1.8x increase of baseline VST count, respectively) consisting in CD3 + cells (80.3% and 62.7%, respectively) with CD4 + dominance (60% in both donors). Higher numbers of VST were obtained from the donor 2 as compared to donor 1. T-cell clonality test showed oligoclonal reproducible peaks on a polyclonal background for both donors. In contrast, VST could be neither expanded nor primed in a donor without evidence of prior infection. This proof-of-concept study supports the feasibility of expanding ex vivo SARS-CoV-2-specific VST from blood of convalescent donors. The results raise the question of whether the selection of seropositive donors may be a strategy to obtain cell lines enriched in their SARS-CoV-2-specificity for future adoptive transfer to immunosuppressed patients.
  • |*COVID-19[MESH]
  • |*SARS-CoV-2[MESH]
  • |Adoptive Transfer[MESH]
  • |CD4-Positive T-Lymphocytes[MESH]


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