<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>39</volume><submitter>Perez-Martinez A</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Effective treatments are still needed to reduce the severity of symptoms, time of hospitalization, and mortality of COVID-19. SARS-CoV-2 specific memory T-lymphocytes obtained from convalescent donors recovered can be used as passive cell immunotherapy.&lt;h4>Methods&lt;/h4>Between September and November 2020 a phase 1, dose-escalation, single centre clinical trial was conducted to evaluate the safety and feasibility of the infusion of CD45RA&lt;sup>-&lt;/sup> memory T cells containing SARS-CoV-2 specific T cells as adoptive cell therapy against moderate/severe cases of COVID-19. Nine participants with pneumonia and/or lymphopenia and with at least one human leukocyte antigen (HLA) match with the donor were infused. The first three subjects received the lowest dose (1 × 10&lt;sup>5&lt;/su</pubmed_abstract><journal>EClinicalMedicine</journal><pagination>101086</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8361305</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Phase I dose-escalation single centre clinical trial to evaluate the safety of infusion of memory T cells as adoptive therapy in COVID-19 (RELEASE).</pubmed_title><pmcid>PMC8361305</pmcid><pubmed_authors>Sanchez-Zapardiel E</pubmed_authors><pubmed_authors>Balas A</pubmed_authors><pubmed_authors>Buckley RM</pubmed_authors><pubmed_authors>Guerra-Garcia P</pubmed_authors><pubmed_authors>Moreno MA</pubmed_authors><pubmed_authors>Arribas JR</pubmed_authors><pubmed_authors>Gasior M</pubmed_authors><pubmed_authors>Mora-Rillo M</pubmed_authors><pubmed_authors>De Paz R</pubmed_authors><pubmed_authors>Vicario JL</pubmed_authors><pubmed_authors>Perez-Martinez A</pubmed_authors><pubmed_authors>Pascual-Miguel B</pubmed_authors><pubmed_authors>Queiruga-Parada J</pubmed_authors><pubmed_authors>Marcos A</pubmed_authors><pubmed_authors>Ferreras C</pubmed_authors><pubmed_authors>Garcia I</pubmed_authors><pubmed_authors>Eguizabal C</pubmed_authors><pubmed_authors>Mestre-Duran C</pubmed_authors><pubmed_authors>Carcas AJ</pubmed_authors><pubmed_authors>Montejano R</pubmed_authors><pubmed_authors>Soria B</pubmed_authors><pubmed_authors>Borobia AM</pubmed_authors><pubmed_authors>Solano C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Phase I dose-escalation single centre clinical trial to evaluate the safety of infusion of memory T cells as adoptive therapy in COVID-19 (RELEASE).</name><description>&lt;h4>Background&lt;/h4>Effective treatments are still needed to reduce the severity of symptoms, time of hospitalization, and mortality of COVID-19. SARS-CoV-2 specific memory T-lymphocytes obtained from convalescent donors recovered can be used as passive cell immunotherapy.&lt;h4>Methods&lt;/h4>Between September and November 2020 a phase 1, dose-escalation, single centre clinical trial was conducted to evaluate the safety and feasibility of the infusion of CD45RA&lt;sup>-&lt;/sup> memory T cells containing SARS-CoV-2 specific T cells as adoptive cell therapy against moderate/severe cases of COVID-19. Nine participants with pneumonia and/or lymphopenia and with at least one human leukocyte antigen (HLA) match with the donor were infused. The first three subjects received the lowest dose (1 × 10&lt;sup>5&lt;/su</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2026-05-09T03:25:53.735Z</modification><creation>2022-02-11T11:20:45.721Z</creation></dates><accession>S-EPMC8361305</accession><cross_references><pubmed>34405140</pubmed><doi>10.1016/j.eclinm.2021.101086</doi></cross_references></HashMap>