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Collagen-binding IL-12 enhances tumour inflammation and drives the complete remission of established immunologically cold mouse tumours

Nature Biomedical Engineer. 2020-04; 
Aslan Mansurov , Jun Ishihara, Peyman Hosseinchi , Lambert Potin , Tiffany M. Marchell , Ako Ishihara, John-Michael Williford, Aaron T. Alpar, Michal M. Raczy, Laura T. Gray, Melody A. Swartz  and Jeffrey A. Hubbell
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Gene Synthesis To produce wild-type IL-12, optimized sequences encoding mouse p35 and p40 subunits were synthesized and subcloned into mammalian expression vector pcDNA3.1(+) by GenScript...Sequences encoding CBD–p35 and p40–CBD were subcloned into the mammalian expression vector pcDNA3.1(+) by GenScript...The peptides used in the restimulation assays were synthesized by GenScript... Get A Quote
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摘要

Checkpoint-inhibitor (CPI) immunotherapy has achieved remarkable clinical success, yet its efficacy in ‘immunologically cold’ tumours has been modest. Interleukin-12 (IL-12) is a powerful cytokine that activates the innate and adaptive arms of the immune system; however, the administration of IL-12 has been associated with immune-related adverse events. Here we show that, after intravenous administration of a collagen-binding domain fused to IL-12 (CBD–IL-12) in mice bearing aggressive mouse tumours, CBD–IL-12 accumulates in the tumour stroma due to exposed collagen in the disordered tumour vasculature. In comparison with the administration of unmodified IL-12, CBD–IL-12 induced sustained intratu... More

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