CRISPR/Cas9 gene editing in hematopoietic stem and progenitor cells to accelerate the translation of cellular therapies and immunotherapies.

Authors

Laura Falceto Font, Dan Jin, John Figg, Connor Francis, Kaytora Long-James, Jeffrey Drake, Alexandra Reid, Caitland Love, Brianna McDonald, David Hilferty, Hector Mendez-Gomez, Rachael Bessey, Fernanda Pohl-Guimarães, Duane Mitchell, Zubaidan Tuerdi, Evelyne Lauret, Catherine Flores

Published in

Journal of translational research. Volume 3. Issue 1. Pages 2660423. Epub Jun 02, 2026.

Abstract

Hematopoietic stem and progenitor cells (HSPCs) play a critical role in immune system regeneration and have therapeutic potential in hematological disorders and immunotherapy. However, gene editing in HSPCs remains challenging, particularly in murine HSPCs, limiting preclinical studies and translational advancements. Here, we present a CRISPR/Cas9 mRNA-based protocol for efficient gene editing of human CD34+ HSPCs and murine HSPCs. Using electroporation of Cas9 mRNA and sgRNAs, we achieved up to 80% gene knock-down in HSPCs while retaining cell viability. Edited murine HSPCs successfully reconstituted bone marrow in lethally irradiated mice, demonstrating functional engraftment. We also demonstrated that knocking-out IL-6R in murine HSPCs and CD34+ cells skewed myeloid differentiation toward less immunosuppressive phenotypes, and combining IL-6R-knock-out murine HSPCs with immune checkpoint inhibitors enhanced glioma treatment efficacy in preclinical models, showcasing the potential of this method to facilitate translation of cellular therapies. This method offers a scalable and cost-effective approach to genetic modification of HSPCs, supporting advancements in hematopoietic stem cell transplants (HSCTs) and next-generation immunotherapies. By streamlining gene editing for both preclinical and translational applications, this protocol has the potential to accelerate the development of personalised cellular therapies and improve clinical outcomes in oncology and immune-related disorders.

PMID:
42802750
Bibliographic data and abstract were imported from PubMed on 28 Sep 2026.

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