Artificial thymic organoid culture generates functional iPSC-derived CD4+ invariant natural killer T cells
Invariant NKT (iNKT) cells have a T-cell receptor that is common to all individuals and are activated by recognizing glycolipids on MHC class I-like CD1d molecules. Activated iNKT cells are known to exert anti-tumor effects through the activation of other immune cells and have attracted attention as promising T cells for eliciting anti-tumor immunity. However, securing a sufficient number of iNKT cells is an obstacle to treatment because iNKT cells are a very small cell population, less than 0.1% of the peripheral blood lymphocytes. Although previous studies have demonstrated redifferentiation of a large number of CD4<sup>-</sup>CD8<sup>-</sup> double-negative iNKT cells from induced pluripotent stem (iPS) cells in two-dimensional monolayer cultures, CD4<sup>+</sup> single-positive (CD4SP) iNKT cells could not be induced. Here we show CD4SP iNKT cells can be obtained by three-dimensional (3D) organoid culture (3D-CD4+ iNKT cell). We additionally describe 3D-CD4+ iNKT cells show antigen-specific helper functions, as they proliferate, produce interferon-γ/interleukin-4 (IFN-γ/IL-4), and induce dendritic cell maturation in response to α-galactosylceramide. Furthermore, they reverse the inhibition of T cell proliferation induced by immunosuppressive macrophages in an antigen-specific manner. Collectively, 3D-CD4+ iNKT cells may become an adjuvant T-cell source to enhance current T-cell immunotherapy against solid tumors.
Authors
- Shin Kaneko
- Sara Shiina
- Shoichi Iriguchi
- Tatsuki Ueda (ORCID: https://orcid.org/0000-0002-6705-5626)
- Yasushi Uemura
Institutions
- Kaneka (United States) (US)
- University of Tsukuba (JP)
- Kyoto University (JP)
- National Cancer Center Hospital East (JP)
- Takeda (Japan) (JP)
Publication Details
- Journal
- Communications Biology
- Published
- 2026-01-09
- DOI
- https://doi.org/10.1038/s42003-025-09462-1
- Primary Topic
- Immune Cell Function and Interaction
- Type
- article
- Field-Weighted Citation Impact
- 0.00