J Leukoc Biol. 2025 Apr 16:qiaf045. doi: 10.1093/jleuko/qiaf045. Online ahead of print.
ABSTRACT
Dendritic cells (DCs) are rare innate immune cells that are essential regulators of anti-tumour, anti-viral and vaccine responses by the adaptive immune system. Conventional dendritic cells, particularly the cDC1 subset, are most desired for DC-based immunotherapies, however, it can be difficult to isolate sufficient numbers of primary cells from patients. The most common alternate sources of DC are ex vivo monocyte-derived DC, although patient-derived monocytes are often dysfunctional. Induced pluripotent stem cells (iPSC) offer a promising solution, providing an opportunity for in vitro generating DCs that are suitable for allogenic off-the-shelf batch-manufactured cells. Here, we developed an in vitro protocol designed to maximise the yield of iPSC-derived DC progenitors, with the specific goal of generating cDC1-like cells. The iPSC-DCs subsets generated by our method could be partitioned by cell surface phenotypes of cDC1, cDC2 and DC3, but they were most transcriptionally similar to monocyte-derived DC (MoDC). Stimulated iPSC-DCs generated pro-inflammatory cytokines, expressed migratory chemokine receptors including CCR7, upregulated co-stimulatory molecules and induced the proliferation of CD4/CD8 T-cells. Altogether these data indicate that iPSC-derived DC have the potential to traffic through lymphatic endothelium and engage productively with T-cells. This method offers a promising step towards an expandable source of allogeneic human dendritic cells for future applications.
PMID:40238941 | DOI:10.1093/jleuko/qiaf045