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• W1969903238 abstract "Recombinant Pseudomonas fluorescens cells, expressing over 40% protein as bovine interferon-gamma (IFN-γ), were chemically fixed to sterilize the culture and amend the bacterial cell wall. When killed and fixed recombinant cells, termed here amended-recombinant-cells (ARCs), were assayed for interferon activity, we obtained the following surprising results: 1) sterilization and fixation did not inactivate ARC-encapsulated IFN-γ; 2) ARC-encapsulated IFN-γ and soluble, recombinant IFN-γ were equally active in vitro but proteolysis was required for release of the ARC cytokine; and 3) ARC-encapsulated IFN-γ was active in vivo with optimal adjuvant activity at a dose about 1000-fold less than previously reported for soluble, recombinant IFN-γ and 100-fold less than doses which induced adverse systemic effects. The mechanism by which ARC-encapsulation increased IFN-γ activity in vivo remains uncertain. However, our in vitro results show that sustained release of soluble IFN-γ is a likely factor. The ARC production and delivery system achieves enhanced adjuvant activity with reduced risk of systemic effects, and the low cost of IFN-γ production offers new opportunities for the use of this important cytokine." @default.
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• W1969903238 date "2005-10-01" @default.
• W1969903238 modified "2023-10-16" @default.
• W1969903238 title "Amended recombinant cells (ARCs™): An economical and surprisingly effective production and delivery vehicle for recombinant bovine IFN-γ" @default.
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• W1969903238 doi "https://doi.org/10.1016/j.jconrel.2005.06.008" @default.
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