卵巢癌细胞通过 IL-15 反式呈递改善 CD34(+) 祖细胞来源 NK 细胞的抗肿瘤功能

Ovarian cancer (OC) is the most lethal gynecological malignancy. As high numbers of Natural Killer (NK) cells in ascites associate with improved survival, the adoptive transfer of allogeneic NK cells is an attractive therapeutic strategy. An approach to further improve NK cell expansion and anti-tumor functionality post-infusion includes IL-15 transpresentation (transIL-15), which involves surface expression of the IL-15 cytokine bound to IL-15R .

However, others have substantiated that systemic administration of ALT/N-803, a soluble molecule mimicking transIL-15, leads to T cell-mediated rejection of the infused allogeneic NK cell product.

In addition, whether transIL-15 induce superior expansion and functionality of our hematopoietic progenitor cell-derived NK cells (HPC-NK) remains understudied.

Here, we propose to transfect OC cells with IL-15 and IL-15R mRNA and evaluate HPC-NK cell stimulation in vitro . Co-transfection of both mRNAs resulted in surface co-expression of both components, thus mimicking the transIL-15.

Importantly, co-culture of HPC-NK cells with transIL-15 OC cells resulted in superior proliferation, IFN production, cytotoxicity and granzyme B secretion.

Furthermore, we observed uptake of IL-15R by HPC-NK cells when co-cultured with transIL-15 OC cells, which associates with NK cell long-term proliferation and survival. Superior killing and granzyme B secretion were also observed in transIL-15 OC spheroids.

Our results demonstrate that local delivery of IL-15 and IL-15R mRNA to OC tumors may be a safer strategy to boost HPC-NK cell therapy of OC through IL-15 transpresentation.