Vaccines (Oct 2021)

Avian Cell Line DuckCelt<sup>®</sup>-T17 Is an Efficient Production System for Live-Attenuated Human Metapneumovirus Vaccine Candidate Metavac<sup>®</sup>

  • Caroline Chupin,
  • Andrés Pizzorno,
  • Aurélien Traversier,
  • Pauline Brun,
  • Daniela Ogonczyk-Makowska,
  • Blandine Padey,
  • Cédrine Milesi,
  • Victoria Dulière,
  • Emilie Laurent,
  • Thomas Julien,
  • Marie Galloux,
  • Bruno Lina,
  • Jean-François Eléouët,
  • Karen Moreau,
  • Marie-Eve Hamelin,
  • Olivier Terrier,
  • Guy Boivin,
  • Julia Dubois,
  • Manuel Rosa-Calatrava

DOI
https://doi.org/10.3390/vaccines9101190
Journal volume & issue
Vol. 9, no. 10
p. 1190

Abstract

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The development of a live-attenuated vaccine (LAV) for the prevention of human metapneumovirus (HMPV) infection is often hampered by the lack of highly efficient and scalable cell-based production systems that support eventual global vaccine production. Avian cell lines cultivated in suspension compete with traditional cell platforms used for viral vaccine manufacture. We investigated whether the DuckCelt®-T17 avian cell line (Vaxxel), previously described as an efficient production system for several influenza strains, could also be used to produce a new HMPV LAV candidate (Metavac®, SH gene-deleted A1/C-85473 HMPV). To that end, we characterized the operational parameters of MOI, cell density, and trypsin addition to achieve the optimal production of Metavac®, and demonstrated that the DuckCelt®-T17 cell line is permissive and well-adapted to the production of the wild-type A1/C-85473 HMPV and the Metavac® vaccine candidate. Moreover, our results confirmed that the LAV candidate produced in DuckCelt®-T17 cells conserves its advantageous replication properties in LLC-MK2 and 3D-reconstituted human airway epithelium models, and its capacity to induce efficient neutralizing antibodies in a BALB/c mouse model. Our results suggest that the DuckCelt®-T17 avian cell line is a very promising platform for the scalable in-suspension serum-free production of the HMPV-based LAV candidate Metavac®.

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