Development of IL-15/IL-15R alpha sushi domain-IgG4 Fc complexes in Pichia pastoris with potent activities and prolonged half-lives

Background Interleukin-15 (IL-15) is a critical cytokine for the development, proliferation, and function of natural killer (NK) cells, NKT cells, and CD8(+) memory T cells and has become one of the most promising protein molecules for the treatment of cancer and viral diseases. However, there are s...

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Veröffentlicht in:Microbial cell factories 2021-06, Vol.20 (1), p.1-115, Article 115
Hauptverfasser: Xu, Huan, Shi, Mingyang, Shao, Changsheng, Li, Hao, Wu, Jing, Yu, Yin, Fang, Fang, Guo, Yugang, Xiao, Weihua
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Sprache:eng
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Zusammenfassung:Background Interleukin-15 (IL-15) is a critical cytokine for the development, proliferation, and function of natural killer (NK) cells, NKT cells, and CD8(+) memory T cells and has become one of the most promising protein molecules for the treatment of cancer and viral diseases. However, there are several limitations in applying IL-15 in therapy, such as its low yield in vitro, limited potency, and short half-life in vivo. To date, there are several recombinant IL-15 agonists based on configurational modifications that are being pursued in the treatment of cancer, such as ALT-803, which are mainly produced from mammalian cells. Results In this study, we designed two different forms of the IL-15 complex, which were formed by the noncovalent assembly of IL-15 with dimeric or monomeric sushi domain of IL-15 receptor alpha (SuIL-15R alpha)-IgG4 Fc fusion protein and designated IL-15/SuIL-15R alpha-dFc and IL-15/SuIL-15R alpha-mFc, respectively. The two IL-15 complexes were expressed in Pichia pastoris (P. pastoris), and their activities and half-lives were evaluated and compared. Pharmacokinetic analysis showed that IL-15/SuIL-15R alpha-dFc had a half-life of 14.26 h while IL-15/SuIL-15R alpha-mFc had a half-life of 9.16 h in mice, which were much longer than the 0.7-h half-life of commercial recombinant human IL-15 (rhIL-15). Treatment of mice with intravenous injection of the two IL-15 complexes resulted in significant increases in NK cells, NKT cells, and memory CD8(+) T cells, which were not observed after rhIL-15 treatment. Treatment of human peripheral blood mononuclear cells (PBMCs) from healthy donors with the two IL-15 complexes yielded enhanced NK and CD8(+) T cell activation and proliferation, which was comparable to the effect of rhIL-15. Conclusions These findings indicate that the IL-15/SuIL-15R alpha-dFc and IL-15/SuIL-15R alpha-mFc produced in P. pastoris exhibit potent activities and prolonged half-lives and may serve as superagonists for immunotherapy in further research and applications.
ISSN:1475-2859
1475-2859
DOI:10.1186/s12934-021-01605-3