Lentiviral Hematopoietic Stem Cell Gene Therapy Benefits Metachromatic Leukodystrophy

被引:965
作者
Biffi, Alessandra [1 ]
Montini, Eugenio [1 ]
Lorioli, Laura [1 ]
Cesani, Martina [1 ]
Fumagalli, Francesca
Plati, Tiziana [1 ]
Baldoli, Cristina
Martino, Sabata
Calabria, Andrea [1 ]
Canale, Sabrina
Benedicenti, Fabrizio [1 ]
Vallanti, Giuliana
Biasco, Luca [1 ]
Leo, Simone
Kabbara, Nabil
Zanetti, Gianluigi
Rizzo, William B.
Mehta, Nalini A. L.
Cicalese, Maria Pia
Casiraghi, Miriam
Boelens, Jaap J.
Del Carro, Ubaldo
Dow, David J.
Schmidt, Manfred
Assanelli, Andrea
Neduva, Victor
Di Serio, Clelia
Stupka, Elia
Gardner, Jason
von Kalle, Christof
Bordignon, Claudio
Ciceri, Fabio
Rovelli, Attilio
Roncarolo, Maria Grazia [1 ]
Aiuti, Alessandro [1 ]
Sessa, Maria
Naldini, Luigi [1 ]
机构
[1] Ist Sci San Raffaele, San Raffaele Telethon Inst Gene Therapy TIGET, I-20132 Milan, Italy
基金
欧洲研究理事会;
关键词
SEVERE COMBINED IMMUNODEFICIENCY; CHRONIC GRANULOMATOUS-DISEASE; CENTRAL-NERVOUS-SYSTEM; GROSS MOTOR FUNCTION; MOUSE MODEL; INTEGRATION SITES; TRANSPLANTATION; VECTOR; SCID-X1; MICROGLIA;
D O I
10.1126/science.1233158
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Metachromatic leukodystrophy (MLD) is an inherited lysosomal storage disease caused by arylsulfatase A (ARSA) deficiency. Patients with MLD exhibit progressive motor and cognitive impairment and die within a few years of symptom onset. We used a lentiviral vector to transfer a functional ARSA gene into hematopoietic stem cells (HSCs) from three presymptomatic patients who showed genetic, biochemical, and neurophysiological evidence of late infantile MLD. After reinfusion of the gene-corrected HSCs, the patients showed extensive and stable ARSA gene replacement, which led to high enzyme expression throughout hematopoietic lineages and in cerebrospinal fluid. Analyses of vector integrations revealed no evidence of aberrant clonal behavior. The disease did not manifest or progress in the three patients 7 to 21 months beyond the predicted age of symptom onset. These findings indicate that extensive genetic engineering of human hematopoiesis can be achieved with lentiviral vectors and that this approach may offer therapeutic benefit for MLD patients.
引用
收藏
页码:864 / U58
页数:12
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