| Literature DB >> 33871182 |
Claire E Repellin1, Marvin A Ssemadaali1, Sherri Newmyer1, Harikrishnan Radhakrishnan1, Harold S Javitz2, Parijat Bhatnagar1,3.
Abstract
The NK-92MI, a fast-growing cytolytic cell line with a track record of exerting clinical efficacy, is transformed into a vector for synthesizing calibrated amounts of desired engineered proteins at our disease site, that is, NK-cell Biofactory. This provides an allogeneic option to the previously published T-cell-based living vector that is limited by high manufacturing cost and product variability. The modularity of this pathway, which combines a "target" receptor with an "effector" function, enables reprogramming of the NK-cell Biofactory to target diseases with specific molecular biomarkers, such as cancer, viral infections, or auto-immune disorders, and overcome barriers that may affect the advancement of NK-cell therapies.Entities:
Keywords: CAR NK cells; CAR T cells; activated T-cells response element; cell engineering; drug delivery; nuclear factor
Mesh:
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Year: 2021 PMID: 33871182 PMCID: PMC8275051 DOI: 10.1002/adbi.202000298
Source DB: PubMed Journal: Adv Biol (Weinh) ISSN: 2701-0198