Haematologica (Nov 2022)

Allogeneic, off-the-shelf, SARS-CoV-2-specific T cells (ALVR109) for the treatment of COVID-19 in high-risk patients

  • Spyridoula Vasileiou,
  • LaQuisa Hill,
  • Manik Kuvalekar,
  • Aster G. Workineh,
  • Ayumi Watanabe,
  • Yovana Velazquez,
  • Suhasini Lulla,
  • Kimberly Mooney,
  • Natalia Lapteva,
  • Bambi J. Grilley,
  • Helen E. Heslop,
  • Cliona M. Rooney,
  • Malcolm K. Brenner,
  • Todd N. Eagar,
  • George Carrum,
  • Kevin A. Grimes,
  • Ann M. Leen,
  • Premal Lulla

DOI
https://doi.org/10.3324/haematol.2022.281946
Journal volume & issue
Vol. 108, no. 7

Abstract

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Defects in T-cell immunity to SARS-CoV-2 have been linked to an increased risk of severe COVID-19 (even after vaccination), persistent viral shedding and the emergence of more virulent viral variants. To address this T-cell deficit, we sought to prepare and cryopreserve banks of virus-specific T cells, which would be available as a partially HLA-matched, off-the-shelf product for immediate therapeutic use. By interrogating the peripheral blood of healthy convalescent donors, we identified immunodominant and protective T-cell target antigens, and generated and characterized polyclonal virus-specific T-cell lines with activity against multiple clinically important SARS-CoV-2 variants (including ‘delta’ and ‘omicron’). The feasibility of making and safely utilizing such virus-specific T cells clinically was assessed by administering partially HLA-matched, third-party, cryopreserved SARS-CoV-2-specific T cells (ALVR109) in combination with other antiviral agents to four individuals who were hospitalized with COVID-19. This study establishes the feasibility of preparing and delivering off-the-shelf, SARS-CoV-2-directed, virus-specific T cells to patients with COVID-19 and supports the clinical use of these products outside of the profoundly immune compromised setting (ClinicalTrials.gov number, NCT04401410).