CRISPR/Cas9-Based Gene Engineering of Human Natural Killer Cells: Protocols for Knockout and Readouts to Evaluate

Mélanie Lambert1, Caroline Leijonhufvud1, Filip Segerberg1

  • 1Center for Hematology and Regenerative Medicine, Department of Medicine, Huddinge, Karolinska Institutet, Stockholm, Sweden.

Insights

CRISPR/Cas9 technology offers a promising new method for genetically engineering natural killer (NK) cells. This approach aims to enhance NK cell-based cancer immunotherapies by improving their cancer-killing ability and persistence.

Area of Science:

  • Immunology
  • Molecular Biology
  • Biotechnology

Background:

  • Natural killer (NK) cells are crucial cytotoxic lymphocytes involved in tumor immune surveillance and cancer treatment.
  • Current adoptive cell therapies using NK cells require improvement in durable response induction.

Observation:

  • Genetic engineering of NK cells can enhance their anti-cancer functions, including cytotoxicity, in vivo persistence, and tumor homing.
  • Previous methods like viral transduction and mRNA electroporation have limitations for NK cell modification.

Findings:

  • CRISPR/Cas9 technology presents a viable alternative for genetically engineering NK cells.
  • Protocols for inducing double-strand breaks in NK cells using CRISPR/Cas9 are detailed, along with efficacy and functional outcome readouts.
  • The advantages and disadvantages of these readouts are discussed.

Implications:

  • CRISPR/Cas9 technology holds potential for advancing NK cell-based cancer therapies.
  • This chapter aims to introduce CRISPR/Cas9 to researchers in the NK cell field.
  • Improved NK cell engineering could lead to more effective cancer immunotherapies.