CRISPR/Cas9-mediated ELANE knockout enables neutrophilic maturation of primary hematopoietic stem and progenitor cells and induced pluripotent stem cells of severe congenital neutropenia patients

• Published in: Haematologica (Roma) Vol. 105; no. 3; pp. 598 - 609
• Main Authors: Nasri, Masoud, Ritter, Malte, Mir, Perihan, Dannenmann, Benjamin, Aghaallaei, Narges, Amend, Diana, Makaryan, Vahagn, Xu, Yun, Fletcher, Breanna, Bernhard, Regine, Steiert, Ingeborg, Hahnel, Karin, Berger, Jürgen, Koch, Iris, Sailer, Brigitte, Hipp, Katharina, Zeidler, Cornelia, Klimiankou, Maksim, Bajoghli, Baubak, Dale, David C, Welte, Karl, Skokowa, Julia
• Format: Journal Article
• Language: English
• Published: Italy Ferrata Storti Foundation 01-03-2020
• Subjects: Congenital Bone Marrow Failure Syndromes; CRISPR-Cas Systems; Hematopoietic Stem Cell Transplantation; Humans; Induced Pluripotent Stem Cells; Mutation; Neutropenia - congenital; Neutropenia - genetics
• ISSN: 0390-6078; 1592-8721
• DOI: 10.3324/haematol.2019.221804

A Autosomal-dominant
mutations are the most common cause of severe congenital neutropenia. Although the majority of congenital neutropenia patients respond to daily granulocyte colony stimulating factor, approximately 15 % do not respond to this cytokine at doses up to 50 μg/kg/day and approximately 15 % of patients will develop myelodysplasia or acute myeloid leukemia. "Maturation arrest," the failure of the marrow myeloid progenitors to form mature neutrophils, is a consistent feature of
associated congenital neutropenia. As mutant neutrophil elastase is the cause of this abnormality, we hypothesized that
associated neutropenia could be treated and "maturation arrest" corrected by a CRISPR/Cas9-sgRNA ribonucleoprotein mediated
knockout. To examine this hypothesis, we used induced pluripotent stem cells from two congenital neutropenia patients and primary hematopoietic stem and progenitor cells from four congenital neutropenia patients harboring
mutations as well as HL60 cells expressing mutant
We observed that granulocytic differentiation of
knockout induced pluripotent stem cells and primary hematopoietic stem and progenitor cells were comparable to healthy individuals. Phagocytic functions, ROS production, and chemotaxis of the
KO (knockout) neutrophils were also normal. Knockdown of
in the mutant
expressing HL60 cells also allowed full maturation and formation of abundant neutrophils. These observations suggest that
CRISPR/Cas9 RNP based
knockout of patients' primary hematopoietic stem and progenitor cells followed by autologous transplantation may be an alternative therapy for congenital neutropenia.