Good manufacturing practice production of an off-the-shelf CD34+ progenitor-derived NK cell product with preserved anti-tumor functionality post-infusion in NOD/SCID/IL2Rgnull mice
The adoptive transfer of natural killer (NK) cells represents a promising cancer therapy due to their intrinsic ability to distinguish between malignant and healthy cells in an allogeneic context, enabling off-the-shelf manufacturing possibilities. On demand availability of cryopreserved advanced therapy medicinal products (ATMPs) could promote enrolment in clinical trials and eventually commercialization with repeated dosing possibilities. However, NK cells are considered highly sensitive to cryopreservation-induced defects, including impaired viability, anti-tumor cytotoxicity, and in vivo expansion capacity. Here, we present the GMP-compliant manufacturing of an off-the-shelf NK cell product (RNK001), derived ex vivo from CD34<sup>+</sup> hematopoietic stem and progenitor cells (HSPCs). To facilitate scalability and reduce hands-on time, the production process was adapted to a G-rex bioreactor, yielding high numbers of a pure CD56<sup>+</sup>CD3<sup>-</sup> NK cell product. Cryopreservation of HSPC-NK cells using an optimized freeze-thaw protocol resulted in a consistently high post-thawing viability of mature and differentiated cells. Surviving HSPC-NK cells post-thawing exhibited enhanced proliferative capacity compared to fresh cells in vitro and their persistence in vivo was similar to that of fresh cells when administrated intravenously or intraperitoneally in NOD/SCID/IL2Rg<sup>null</sup> mice. Moreover, cryopreserved HSPC-NK cells had robust anti-tumor functionality, efficiently killing tumor spheroids embedded in a 3D collagen matrix and maintaining degranulation and interferon-γ production capacity comparable to fresh cells following in vivo infusion. Together, these findings show the potential of cryopreserved HSPC-NK cells with potent effector functions, allowing the manufacturing of an off-the-shelf therapeutical NK cell product for hematological and solid malignancies.
Authors
- Anniek B. van der Waart (ORCID: https://orcid.org/0000-0001-5986-3060)
- Anna L. de Goede (ORCID: https://orcid.org/0000-0002-7176-6156)
- Vanessa Rodríguez‐Fanjul (ORCID: https://orcid.org/0000-0002-3386-5874)
- Joop H. Jansen (ORCID: https://orcid.org/0000-0001-9459-568X)
- Harry Dolstra (ORCID: https://orcid.org/0000-0002-3998-687X)
- Diede van Ens (ORCID: https://orcid.org/0000-0001-7273-4896)
- Willemijn Hobo (ORCID: https://orcid.org/0000-0002-8206-8185)
- Marcos Vidal-Manrique (ORCID: https://orcid.org/0000-0002-6596-0876)
- Paul K.J.D. de Jonge (ORCID: https://orcid.org/0000-0002-1228-5002)
- Suzanne van Dorp (ORCID: https://orcid.org/0000-0002-9742-674X)
- Laura Hooijmaijers (ORCID: https://orcid.org/0000-0002-2691-8931)
- Bart Spils
Institutions
- Radboud University Nijmegen (NL)
- Radboud University Medical Center (NL)
- Radboud Institute for Molecular Life Sciences (NL)
Publication Details
- Journal
- Cellular and Molecular Life Sciences
- Published
- 2025-05-26
- DOI
- https://doi.org/10.1007/s00018-025-05727-4
- Citations
- 5
- Primary Topic
- Immune Cell Function and Interaction
- Type
- article
- Field-Weighted Citation Impact
- 3.99
Funders
- KWF Kankerbestrijding
- Radboud Universitair Medisch Centrum