A Killer Disarmed: Natural Killer Cell Impairment in Myelodysplastic Syndrome

Cells. 2023 Feb 16;12(4):633. doi: 10.3390/cells12040633.

Abstract

Myelodysplastic syndrome (MDS) treatment remains a big challenge due to the heterogeneous nature of the disease and its ability to progress to acute myeloid leukemia (AML). The only curative option is allogeneic hematopoietic stem cell transplantation (HSCT), but most patients are unfit for this procedure and are left with only palliative treatment options, causing a big unmet need in the context of this disease. Natural killer (NK) cells are attractive candidates for MDS immunotherapy due to their ability to target myeloid leukemic cells without prior sensitization, and in recent years we have seen an arising number of clinical trials in AML and, recently, MDS. NK cells are reported to be highly dysfunctional in MDS patients, which can be overcome by adoptive NK cell immunotherapy or activation of endogenous NK cells. Here, we review the role of NK cells in MDS, the contribution of the tumor microenvironment (TME) to NK cell impairment, and the most recent data from NK cell-based clinical trials in MDS.

Keywords: acute myeloid leukemia; cancer; immunotherapy; myelodysplastic syndrome; natural killer cells; tumor microenvironment.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Humans
  • Immunotherapy, Adoptive
  • Killer Cells, Natural
  • Leukemia, Myeloid, Acute* / pathology
  • Myelodysplastic Syndromes* / pathology
  • Transplantation, Homologous
  • Tumor Microenvironment

Grants and funding

M.S. was funded by Novamune Ltd. during the drafting of this review.