Evidence map›Paper›PMID 41423621›Full record

ArticleStem cell research & therapy2025

CRISPR editing of HPFH3 genotype induces γ-globin expression and reverses sickle cell disease and β-thalassemia phenotypes.

Sangam Giri Goswami, Pragya Gupta, V R Arvinden, Nupur Bhargava, Aditya Ramdas Iyer, Vinodh Saravanakumar, Poonam Yadav, Somesh K Jha, Shivani Singh, Ajay Kumar and 8 more

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Article in Stem cell research & therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

18 authors.

Sangam Giri Goswami *CSIR- Institute for Genomics and Integrative Biology, Mathura Road, Sukhdev Vihar, New Delhi, 110025, India.
Pragya Gupta *CSIR- Institute for Genomics and Integrative Biology, Mathura Road, Sukhdev Vihar, New Delhi, 110025, India.
V R ArvindenCSIR- Institute for Genomics and Integrative Biology, Mathura Road, Sukhdev Vihar, New Delhi, 110025, India.
Nupur BhargavaCSIR- Institute for Genomics and Integrative Biology, Mathura Road, Sukhdev Vihar, New Delhi, 110025, India.
Aditya Ramdas IyerCSIR- Institute for Genomics and Integrative Biology, Mathura Road, Sukhdev Vihar, New Delhi, 110025, India.
Vinodh SaravanakumarCSIR- Institute for Genomics and Integrative Biology, Mathura Road, Sukhdev Vihar, New Delhi, 110025, India.
Poonam YadavLaboratory of Nanotechnology and Chemical Biology, Regional Centre for Biotechnology, NCR Biotech Science Cluster, 3Rd Milestone, Faridabad-Gurgaon Expressway, Faridabad, Haryana, 121001, India.
Somesh K JhaLaboratory of Nanotechnology and Chemical Biology, Regional Centre for Biotechnology, NCR Biotech Science Cluster, 3Rd Milestone, Faridabad-Gurgaon Expressway, Faridabad, Haryana, 121001, India.
Shivani SinghCSIR- Institute for Genomics and Integrative Biology, Mathura Road, Sukhdev Vihar, New Delhi, 110025, India.
Ajay KumarCSIR- Institute for Genomics and Integrative Biology, Mathura Road, Sukhdev Vihar, New Delhi, 110025, India.
Praveen SinghCSIR- Institute for Genomics and Integrative Biology, Mathura Road, Sukhdev Vihar, New Delhi, 110025, India.
Padma GundaThalassemia and Sickle Cell Society- Kamala Hospital and Research Centre, Shivarampally, Hyderabad, 5000052, India.
Suman JainThalassemia and Sickle Cell Society- Kamala Hospital and Research Centre, Shivarampally, Hyderabad, 5000052, India.
Pallavi MehtaRajiv Gandhi Cancer Institute and Research Institute and Research Centre, Rohini, Delhi, 110085, India.
Yukio NakamuraCell Engineering Division, RIKEN BioResource, Research Center, Ibaraki, 3050074, Japan.
Ryo KuritaCell Engineering Division, RIKEN BioResource, Research Center, Ibaraki, 3050074, Japan.
Avinash BajajLaboratory of Nanotechnology and Chemical Biology, Regional Centre for Biotechnology, NCR Biotech Science Cluster, 3Rd Milestone, Faridabad-Gurgaon Expressway, Faridabad, Haryana, 121001, India.
Sivaprakash RamalingamCSIR- Institute for Genomics and Integrative Biology, Mathura Road, Sukhdev Vihar, New Delhi, 110025, India. sivaprakash@iitk.ac.in.ORCID http://orcid.org/0009-0002-9205-2547

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHereditary persistence of Fetal Hemoglobin (HPFH) is a benign condition known to mitigate symptoms in individuals with co-inherited β-hemoglobinopathies, such as β-thalassemia (BT) and sickle cell disease (SCD), through the reactivation of fetal hemoglobin (HbF). HPFH typically arises from deletions of varying sizes affecting the β-globin gene cluster or point mutations in the promoters of the γ-globin genes. While the therapeutic benefits of point mutations have been extensively studied, the potential of deletional forms of HPFH remains underexplored in preclinical settings.

methodIn this study, we generated benign deletional HPFH3 genotype in SCD and BT patient-derived HSPCs using CRISPR/Cas9 and showed that therapeutically relevant levels of HbF reactivation result in the alleviation of the pathological phenotypes.

resultsIn edited cells derived from SCD patients, we observed reduced sickling and oxidative stress, while in edited from BT cells, restoration of the α-globin/β-globin ratio improved erythroid lineage maturation and reduced ROS levels. Importantly, HPFH3-edited HSPCs retained their genome integrity and showed no detrimental effect on their regeneration or differentiation into erythroid, myeloid, T, and B cell lineages in immunodeficient NBSGW mice post-xenotransplantation. Additionally, we showed a reduced interaction between the LCR and HBB, suggesting that the HPFH3 deletion specifically promoted LCR interactions with HBG1/2, likely due to the absence of the HBB locus.

conclusionsCollectively, our preclinical findings suggest that the generation of the HPFH3 genotype has the potential to significantly enhance HbF levels, offering a promising universal therapeutic strategy for treating both SCD and β-thalassemia.

Indexed as

Anemia, Sickle Cellbeta-ThalassemiaFetal Hemoglobingamma-GlobinsGene EditingAnimalsCRISPR-Cas SystemsGenotypeHematopoietic Stem CellsHumansMicePhenotypeFetal Hemoglobingamma-GlobinsCellCRISPR/Cas9Fetal hemoglobinGene therapyHPFHSickle cell diseaseβ-thalassemia

Identifiers

PMID41423621
PMCPMC12836809

What Socratic holds

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LicenceCC BY-NC-ND
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.