Large-scale generation of iNK and CAR-iNK cells from CD34⁺ haematopoietic stem and progenitor cells for adoptive immunotherapy.

Abstract

Chimaeric antigen receptor (CAR) natural killer (CAR-NK) cells are a promising alternative to CAR-T cells for immunotherapies. High and multiple doses of CAR-NK cell infusions are essential to maintain therapeutic efficacy in clinical trials, requiring efficient methods for generating CAR-NK cells at scale. Here we develop a three-step strategy to generate high yields of induced NK (iNK) and CAR-iNK cells from human umbilical cord blood CD34⁺ haematopoietic stem and progenitor cells (CD34⁺ HSPCs). Starting from a single umbilical cord blood CD34⁺ HSPC, our reliable method efficiently produces 14-83 million mature iNK cells or 7-32 million CAR-iNK cells with high expression levels of CD16 and zero T-cell contamination. Both fresh and thawed iNK and CAR-iNK cells demonstrate anti-tumour activities against various human cancer cells and prolong the survival of human tumour-bearing animals. The high yields of CAR-NK cells and reduced costs of our method's CAR engineering support the broad applications of these cells for treating cancer patients.