CAR-NK cells derived from cord blood originate mainly from CD56-CD7+CD34-HLA-DR-Lin- NK progenitor cells.

Abstract

Cord blood (CB)-derived chimeric antigen receptor (CAR)-natural killer (NK) cells targeting CD19 have been shown to be effective against B cell malignancies. While human CD56⁺ NK cells can be expanded in vitro, NK cells can also be differentiated from hematopoietic progenitor cells. It is still unclear whether CAR-NK cells originate from mature NK cells or NK progenitor cells in CB. Here, we determined that CAR-NK cells were predominantly derived from CD56^- NK progenitor cells. We first found that substantial numbers of CD19 CAR-NK cells were produced from CD56^- CB mononuclear cells after in vitro culture for 2 weeks. Single-cell RNA sequencing analysis of CD56^-CD3^-CD14^-CD19^- CB mononuclear cells revealed that these cells could be subdivided into three subpopulations based on the expression of CD34 and human leukocyte antigen (HLA)-DR. NK cells originated primarily from CD34^-HLA-DR^- cells. In addition, among the CD34^-HLA-DR^- cells, only CD7⁺ cells could differentiate into NK cells. These results indicate that CD56^-CD7⁺CD34^-HLA-DR^- lineage marker (Lin)^- cells are the major origin of human CB-derived CAR-NK cells, indicating the importance of developing methods to enhance the quality and quantity of NK cells produced from these NK progenitor cells.