Molecular TherapyMolecular BiologyPeer-reviewed journal article
Aberrant Clonal Hematopoiesis Following Lentiviral Transduction of HSPC in a Rhesus Macaque
Diego A. EspinozaiD, Xing FaniD, Di YangiD, Stefan CordesiD, Lauren L. TruittiD, Katherine R. CalvoiD, Idalia M. Yabe, Selami DemirciiD, Kristin J. HopeiD, So Gun HongiD, Allen E. Krouse, Mark E. Metzger, Aylin C. Bonifacino, Rong LuiD, Naoya UchidaiD, John F. TisdaleiD, Xiaolin WuiD, Suk See De RaviniD, Harry L. MalechiD, Robert E. DonahueiD, Chuanfeng WuiD, Cynthia E. DunbariD
Abstract
Lentiviral vectors (LV) have been used for the delivery of genes into hematopoietic stem and progenitor cells (HSPC) in clinical trials worldwide. LV, in contrast to retroviral vectors, have not been associated with insertion site-associated malignant clonal expansions, and thus have been considered safer. Here, however, we present a case of markedly abnormal dysplastic clonal hematopoiesis impacting the erythroid, myeloid and megakaryocytic lineages in a rhesus macaque transplanted with HSPCs that were transduced with a LV containing a strong retroviral murine stem cell virus (MSCV) constitutive promoter-enhancer in the LTR. 9 insertions were mapped in the abnormal clone, resulting in overexpression and aberrant splicing of several genes of interest, including the cytokine stem cell factor and the transcription factor PLAG1. This case represents the first clear link between a lentiviral insertion-induced clonal expansion and a clinically abnormal transformed phenotype following transduction of normal primate or human HSPC, and are thus concerning, and suggest that strong constitutive promoters should not be included within LV vectors.
- organism: rat
- assay: bulk RNA-seq
- research focus: cell type annotation
- research focus: differential expression
- research focus: gene regulatory network inference
- approach: experimental assay
- Citations
- 43
- FWCI
- 3.75
- Field percentile
- top 6%
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