Literature DB >> 33283990

Post-Transcriptional Genetic Silencing of BCL11A to Treat Sickle Cell Disease.

Erica B Esrick1, Leslie E Lehmann1, Alessandra Biffi1, Maureen Achebe1, Christian Brendel1, Marioara F Ciuculescu1, Heather Daley1, Brenda MacKinnon1, Emily Morris1, Amy Federico1, Daniela Abriss1, Kari Boardman1, Radia Khelladi1, Kit Shaw1, Helene Negre1, Olivier Negre1, Sarah Nikiforow1, Jerome Ritz1, Sung-Yun Pai1, Wendy B London1, Colleen Dansereau1, Matthew M Heeney1, Myriam Armant1, John P Manis1, David A Williams1.   

Abstract

BACKGROUND: Sickle cell disease is characterized by hemolytic anemia, pain, and progressive organ damage. A high level of erythrocyte fetal hemoglobin (HbF) comprising α- and γ-globins may ameliorate these manifestations by mitigating sickle hemoglobin polymerization and erythrocyte sickling. BCL11A is a repressor of γ-globin expression and HbF production in adult erythrocytes. Its down-regulation is a promising therapeutic strategy for induction of HbF.
METHODS: We enrolled patients with sickle cell disease in a single-center, open-label pilot study. The investigational therapy involved infusion of autologous CD34+ cells transduced with the BCH-BB694 lentiviral vector, which encodes a short hairpin RNA (shRNA) targeting BCL11A mRNA embedded in a microRNA (shmiR), allowing erythroid lineage-specific knockdown. Patients were assessed for primary end points of engraftment and safety and for hematologic and clinical responses to treatment.
RESULTS: As of October 2020, six patients had been followed for at least 6 months after receiving BCH-BB694 gene therapy; median follow-up was 18 months (range, 7 to 29). All patients had engraftment, and adverse events were consistent with effects of the preparative chemotherapy. All the patients who could be fully evaluated achieved robust and stable HbF induction (percentage HbF/(F+S) at most recent follow-up, 20.4 to 41.3%), with HbF broadly distributed in red cells (F-cells 58.9 to 93.6% of untransfused red cells) and HbF per F-cell of 9.0 to 18.6 pg per cell. Clinical manifestations of sickle cell disease were reduced or absent during the follow-up period.
CONCLUSIONS: This study validates BCL11A inhibition as an effective target for HbF induction and provides preliminary evidence that shmiR-based gene knockdown offers a favorable risk-benefit profile in sickle cell disease. (Funded by the National Institutes of Health; ClinicalTrials.gov number, NCT03282656).
Copyright © 2020 Massachusetts Medical Society.

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Year:  2020        PMID: 33283990      PMCID: PMC7962145          DOI: 10.1056/NEJMoa2029392

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


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