In Vivo Tracking of Human Hematopoiesis Reveals Patterns of Clonal Dynamics during Early and Steady-State Reconstitution Phases

被引:192
作者
Biasco, Luca [1 ]
Pellin, Danilo [2 ]
Scala, Serena [1 ]
Dionisio, Francesca [1 ]
Basso-Ricci, Luca [1 ]
Leonardelli, Lorena [1 ]
Scaramuzza, Samantha [1 ]
Baricordi, Cristina [1 ]
Ferrua, Francesca [1 ,3 ]
Cicalese, Maria Pia [1 ,3 ]
Giannelli, Stefania [1 ]
Neduva, Victor [4 ]
Dow, David J. [4 ]
Schmidt, Manfred [5 ]
Von Kalle, Christof [5 ]
Roncarolo, Maria Grazia [1 ,6 ]
Ciceri, Fabio [3 ]
Vicard, Paola [7 ]
Wit, Ernst [8 ]
Di Serio, Clelia [2 ,9 ]
Naldini, Luigi [1 ,9 ]
Aiuti, Alessandro [1 ,3 ,9 ]
机构
[1] San Raffaele Telethon Inst Gene Therapy TIGET, I-20132 Milan, Italy
[2] Univ Vita Salute San Raffaele, CUSSB, I-20132 Milan, Italy
[3] Ist Sci San Raffaele, Pediat Immunohematol & Bone Marrow Transplant Uni, I-20132 Milan, Italy
[4] GlaxoSmithKline R&D, Target Sci, Stevenage SG1 2NY, Herts, England
[5] German Canc Res Ctr, Natl Ctr Tumor Dis NCT, D-69121 Heidelberg, Germany
[6] Stanford Sch Med, Div Stem Cell Transplantat & Regenerat Med, Dept Pediat, Stanford, CA 94305 USA
[7] Univ Roma Tre, Dept Econ, I-00154 Rome, Italy
[8] Univ Groningen, Johann Bernoulli Inst, NL-9700 AB Groningen, Netherlands
[9] Univ Vita Salute San Raffaele, I-20132 Milan, Italy
关键词
WISKOTT-ALDRICH-SYNDROME; STEM-CELL TRANSPLANTATION; MYELOID-BASED MODEL; HUMAN CORD BLOOD; GENE-THERAPY; LENTIVIRAL VECTOR; SCID PATIENTS; BONE-MARROW; PROGENITORS; IMMUNODEFICIENCY;
D O I
10.1016/j.stem.2016.04.016
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
Hematopoietic stem/progenitor cells (HSPCs) are capable of supporting the lifelong production of blood cells exerting a wide spectrum of functions. Lentiviral vector HSPC gene therapy generates a human hematopoietic system stably marked at the clonal level by vector integration sites (ISs). Using IS analysis, we longitudinally tracked > 89,000 clones from 15 distinct bone marrow and peripheral blood lineages purified up to 4 years after transplant in four Wiskott-Aldrich syndrome patients treated with HSPC gene therapy. We measured at the clonal level repopulating waves, populations' sizes and dynamics, activity of distinct HSPC subtypes, contribution of various progenitor classes during the early and late post-transplant phases, and hierarchical relationships among lineages. We discovered that invitro-manipulated HSPCs retain the ability to return to latency after transplant and can be physiologically reactivated, sustaining a stable hematopoietic output. This study constitutes in vivo comprehensive tracking in humans of hematopoietic clonal dynamics during the early and late post-transplant phases.
引用
收藏
页码:107 / 119
页数:13
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