A method to sequence and quantify DNA integration for monitoring outcome in gene therapy

被引:61
作者
Brady, Troy [1 ]
Roth, Shoshannah L. [1 ]
Malani, Nirav [1 ]
Wang, Gary P. [1 ]
Berry, Charles C. [2 ]
Leboulch, Philippe [3 ,4 ,5 ,6 ,7 ]
Hacein-Bey-Abina, Salima [8 ]
Cavazzana-Calvo, Marina [8 ]
Papapetrou, Eirini P. [9 ,10 ]
Sadelain, Michel [9 ,10 ]
Savilahti, Harri [11 ]
Bushman, Frederic D. [1 ]
机构
[1] Univ Penn, Sch Med, Dept Microbiol, Philadelphia, PA 19104 USA
[2] Univ Calif San Diego, Sch Med, Dept Family Prevent Med, San Diego, CA 92093 USA
[3] Inst Emerging Dis & Innovat Therapies iMETI, Commissariat Energie Atom & Energies Alternat, F-92265 Fontenay Aux Roses, France
[4] INSERM, U962, F-92265 Fontenay Aux Roses, France
[5] Univ Paris 11, F-92265 Fontenay Aux Roses, France
[6] Brigham & Womens Hosp, Div Genet, Boston, MA 02115 USA
[7] Harvard Univ, Sch Med, Boston, MA 02115 USA
[8] Univ Paris 05, Grp Hosp Univ Ouest, Hop Necker Enfants Malad,Dept Biotherapy, AP HP,Ctr Invest Clin Integre Biotherapies,INSERM, Paris, France
[9] Mem Sloan Kettering Canc Ctr, Ctr Cell Engn, New York, NY 10065 USA
[10] Mem Sloan Kettering Canc Ctr, Mol Pharmacol & Chem Program, New York, NY 10065 USA
[11] Univ Turku, Dept Biol, Div Genet & Physiol, Turku 20014, Finland
关键词
SEVERE COMBINED IMMUNODEFICIENCY; TARGET SITE SELECTION; HUMAN GENOME; VECTOR INTEGRATION; BACTERIOPHAGE MU; IN-VITRO; SCID-X1; CELLS; TRANSPOSITION; METHYLATIONS;
D O I
10.1093/nar/gkr140
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human genetic diseases have been successfully corrected by integration of functional copies of the defective genes into human cells, but in some cases integration of therapeutic vectors has activated proto-oncogenes and contributed to leukemia. For this reason, extensive efforts have focused on analyzing integration site populations from patient samples, but the most commonly used methods for recovering newly integrated DNA suffer from severe recovery biases. Here, we show that a new method based on phage Mu transposition in vitro allows convenient and consistent recovery of integration site sequences in a form that can be analyzed directly using DNA barcoding and pyrosequencing. The method also allows simple estimation of the relative abundance of gene-modified cells from human gene therapy subjects, which has previously been lacking but is crucial for detecting expansion of cell clones that may be a prelude to adverse events.
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页数:8
相关论文
共 46 条
[1]   Correction of ADA-SCID by stem cell gene therapy combined with nonmyeloablative conditioning [J].
Aiuti, A ;
Slavin, S ;
Aker, M ;
Ficara, F ;
Deola, S ;
Mortellaro, A ;
Morecki, S ;
Andolfi, G ;
Tabucchi, A ;
Carlucci, F ;
Marinello, E ;
Cattaneo, F ;
Vai, S ;
Servida, P ;
Miniero, R ;
Roncarolo, MG ;
Bordignon, C .
SCIENCE, 2002, 296 (5577) :2410-2413
[2]   Multilineage hematopoietic reconstitution without clonal selection in ADA-SCID patients treated with stem cell gene therapy [J].
Aiuti, Alessandro ;
Cassani, Barbara ;
Andolfi, Grazia ;
Mirolo, Massimiliano ;
Biasco, Luca ;
Recchia, Alessandra ;
Urbinati, Fabrizia ;
Valacca, Cristina ;
Scaramuzza, Samantha ;
Aker, Memet ;
Slavin, Shimon ;
Cazzola, Matteo ;
Sartori, Daniela ;
Ambrosi, Alessandro ;
Di Serio, Clelia ;
Roncarolo, Maria Grazia ;
Mavilio, Fulvio ;
Bordignon, Claudio .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (08) :2233-2240
[3]   High-resolution profiling of histone methylations in the human genome [J].
Barski, Artern ;
Cuddapah, Suresh ;
Cui, Kairong ;
Roh, Tae-Young ;
Schones, Dustin E. ;
Wang, Zhibin ;
Wei, Gang ;
Chepelev, Iouri ;
Zhao, Keji .
CELL, 2007, 129 (04) :823-837
[4]   Selection of target sites for mobile DNA integration in the human genome [J].
Berry, Charles ;
Hannenhalli, Sridhar ;
Leipzig, Jeremy ;
Bushman, Frederic D. .
PLOS COMPUTATIONAL BIOLOGY, 2006, 2 (11) :1450-1462
[5]   The Use of Coded PCR Primers Enables High-Throughput Sequencing of Multiple Homolog Amplification Products by 454 Parallel Sequencing [J].
Binladen, Jonas ;
Gilbert, M. Thomas P. ;
Bollback, Jonathan P. ;
Panitz, Frank ;
Bendixen, Christian ;
Nielsen, Rasmus ;
Willerslev, Eske .
PLOS ONE, 2007, 2 (02)
[6]   Integration target site selection by a resurrected human endogenous retrovirus [J].
Brady, Troy ;
Lee, Young Nam ;
Ronen, Keshet ;
Malani, Nirav ;
Berry, Charles C. ;
Bieniasz, Paul D. ;
Bushman, Frederic D. .
GENES & DEVELOPMENT, 2009, 23 (05) :633-642
[7]   HIV integration site distributions in resting and activated CD4+ T cells infected in culture [J].
Brady, Troy ;
Agosto, Luis M. ;
Malani, Nirav ;
Berry, Charles C. ;
O'Doherty, Una ;
Bushman, Frederic .
AIDS, 2009, 23 (12) :1461-1471
[8]  
Bushman F.D., 2001, LATERAL DNA TRANSFER
[9]   Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease [J].
Cavazzana-Calvo, M ;
Hacein-Bey, S ;
Basile, CD ;
Gross, F ;
Yvon, E ;
Nusbaum, P ;
Selz, F ;
Hue, C ;
Certain, S ;
Casanova, JL ;
Bousso, P ;
Le Deist, F ;
Fischer, A .
SCIENCE, 2000, 288 (5466) :669-672
[10]   Transfusion independence and HMGA2 activation after gene therapy of human β-thalassaemia [J].
Cavazzana-Calvo, Marina ;
Payen, Emmanuel ;
Negre, Olivier ;
Wang, Gary ;
Hehir, Kathleen ;
Fusil, Floriane ;
Down, Julian ;
Denaro, Maria ;
Brady, Troy ;
Westerman, Karen ;
Cavallesco, Resy ;
Gillet-Legrand, Beatrix ;
Caccavelli, Laure ;
Sgarra, Riccardo ;
Maouche-Chretien, Leila ;
Bernaudin, Francoise ;
Girot, Robert ;
Dorazio, Ronald ;
Mulder, Geert-Jan ;
Polack, Axel ;
Bank, Arthur ;
Soulier, Jean ;
Larghero, Jerome ;
Kabbara, Nabil ;
Dalle, Bruno ;
Gourmel, Bernard ;
Socie, Gerard ;
Chretien, Stany ;
Cartier, Nathalie ;
Aubourg, Patrick ;
Fischer, Alain ;
Cornetta, Kenneth ;
Galacteros, Frederic ;
Beuzard, Yves ;
Gluckman, Eliane ;
Bushman, Frederick ;
Hacein-Bey-Abina, Salima ;
Leboulch, Philippe .
NATURE, 2010, 467 (7313) :318-U94