Literature DB >> 31023523

Aberrant Clonal Hematopoiesis following Lentiviral Vector Transduction of HSPCs in a Rhesus Macaque.

Diego A Espinoza1, Xing Fan2, Di Yang3, Stefan F Cordes2, Lauren L Truitt2, Katherine R Calvo2, Idalia M Yabe2, Selami Demirci4, Kristin J Hope5, So Gun Hong2, Allen Krouse2, Mark Metzger2, Aylin Bonifacino2, Rong Lu6, Naoya Uchida4, John F Tisdale4, Xiaolin Wu7, Suk See DeRavin8, Harry L Malech8, Robert E Donahue2, Chuanfeng Wu9, Cynthia E Dunbar10.   

Abstract

Lentiviral vectors (LVs) are used for delivery of genes into hematopoietic stem and progenitor cells (HSPCs) in clinical trials worldwide. LVs, in contrast to retroviral vectors, are not associated with insertion site-associated malignant clonal expansions and, thus, are considered safer. Here, however, we present a case of markedly abnormal dysplastic clonal hematopoiesis affecting 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. Nine 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 lentiviral insertion-induced clonal expansion and a clinically abnormal transformed phenotype following transduction of normal primate or human HSPCs, which is concerning, and suggests that strong constitutive promoters should not be included in LVs. Published by Elsevier Inc.

Entities:  

Keywords:  gene therapy; genotoxicity; lentiviral vector; non-human primate

Mesh:

Substances:

Year:  2019        PMID: 31023523      PMCID: PMC6554657          DOI: 10.1016/j.ymthe.2019.04.003

Source DB:  PubMed          Journal:  Mol Ther        ISSN: 1525-0016            Impact factor:   11.454


  72 in total

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