Presentation at The Annual American Society of Hematology (ASH) Conference: Hematopoietic Stem Cell Gene Therapy Trial with Lentiviral Vector in X-Linked Adrenoleukodystrophy

821 Hematopoietic Stem Cell Gene Therapy Trial with Lentiviral Vector in X-Linked Adrenoleukodystrophy

Clinically Relevant Abstract
Tuesday, December 9, 2008: 8:00 AM
304-306-308 - South (Moscone Center)

Marina Cavazzana-Calvo, MD, PhD1, Nathalie Cartier2*, Salima Hacein-Bey Abina1*, Gabor Veres3*, Manfred Schmidt4*, Cynthia Bartholomae4*, Michel Vidaud5*, Liliane Dal-Cortivo1*, Laure Caccavelli1*, Nizar Malhaoui6*, Pierre Frange6*, Veronique Kiermer7*, Denice Mittelstaedt7*, Andrew Simmons7*, Cline Bellesme2*, Francois Lefrore1*, Chantale Lagresle1*, Stephane Blanche6*, Pierre Charneau8*, Muriel Audit9*, Bruno L'Homme5*, Jing Chao Zhao-Emonet5*, Serge Fichelson10*, Francoise Pflumio10*, Anne Dubart-Kupperschmitt10*, <a data-cke-saved-href="http://www.stopald.org/about/people.asp" href="http://www.stopald.org/about/people.asp">Rachel Salzman11</a>*,&nbsp;<a data-cke-saved-href="http://www.stopald.org/about/people.asp" href="http://www.stopald.org/about/people.asp">Amber Salzman11</a>*, Pierre Bougnores2*, Christof Von Kalle4*, Alain Fischer, MD, PhD12* and Patrick Aubourg2*

1Biotharapie, Hopital Necker - Enfants Malades, Paris, France
2Endocrinologie et Neurologie Pediatrique, AP-HP Hopital Saint Vincent de Paul, Paris, France
3Applied Genetic Technologies, Corporation, Alachua, FL
4Translational Oncology, National Center for Tumor Diseases (NCT) / German Cancer Research Center (DKFZ), Heidelberg, Germany
5Facult des Sciences Pharmaceutiques et Biologiques, UMR745 Inserm, University Paris Descartes,, Paris, France
6Unit d'Immunologie et Hematologie Pediatrique, AP-HP Hopital Necker - Enfants Malades, Paris, France
7Cell Genesys, Inc., San Francisco, CA
8CNRS-URA3015, Institut Pasteur, Paris, France
9Genathon, Paris, France
10departement d'Hematologie - INSERM U567, Institut Cochin, Paris, France
11The StopALD Foundation, Houston, TX
12Service d'Immunologie et Hematologie Pediatrique, INSERM, University Paris Descartes, IFR94, AP-HP Hopital Necker Enfants-Malades, Paris, France

We report preliminary results in 3 children with cerebral X-linked adrenoleukodystrophy (ALD) who received in September 2006, January 2007 and June 2008 lentiviral vector transduced autologous hematopoietic stem cell (HSC). We have previously demonstrated that cerebral demyelination associated with cerebral ALD can be stopped or reversed within 12-18 months by allogeneic HSC transplantation. The long term beneficial effects of HCT transplantation in ALD are due to the progressive turn-over of brain macrophages (microglia) derived from bone-marrow cells. For the current HSC gene therapy procedure, we used mobilized peripheral blood CD34+ cells that were transduced ex vivo for 18 hours with a non-replicative HIV1-derived lentiviral vector (CG1711 hALD) at MOI25 and expressing the ALD cDNA under the control of the MND (myeloproliferative sarcoma virus enhancer, negative control region deleted, dl587rev primer binding site substituted) promoter, and in the presence of 4 human recombinant cytokines (Il-3, Stem Cell Factor [SCF], Flt3-ligand and Megakaryocyte Growth and Differentiation Factor [MGDF]) and CH-296 retronectine. Transduced cells were frozen to perform the required (RCL) safety tests. After thawing and prior to reinjection, 50%, 30% and 40% of transduced CD34+ cells expressed the ALD protein with a mean of 0.7, 0.6 and 0.65 copies of integrated provirus per cell. Transduced CD34+ cells were infused to ALD patients after a conditioning regimen including full doses of cyclophosphamide and busulfan. Hematopoietic recovery occured at day 13-15 post-transplant and the procedure was uneventful. In patient P1 and P2, the percentage of lymphocytes and monocytes expressing the ALD protein declined from day 60 to 6 months after gene therapy (GT) and remained stable up to 16 months post-GT. In P1, 9 to 13% of CD14+, CD3+, CD19+ and CD15+ cells expressed ALD protein 16 months post-transplant. In P2 and at the same time-point after transplant, 10 to 18% of CD14+, CD3+, CD19+ and CD15+ cells expressed ALD protein. ALD protein was expressed in 18-20% of bone marrow CD34+ cells from patients P1 and P2, 12 months post-transplant. In patient P3, 20 to 23% of CD3+, CD14+ and CD15+ cells expressed ALD protein 2 months after transplant. Tests assessing vector-derived RCL and vector mobilization were negative up to the last follow-ups in the 3 patients. Integration of the vector was polyclonal and studies of integration sites arein progress. At 16 months post-transplant, HSC gene therapy resulted in neurological effects comparable with allogeneic HSC transplantation in patient P1 and P2.

These results support that: 1) ex-vivo HSC gene therapy using HIV1-derived lentiviral vector is not associated with the emergence of RCL and vector mobilization ; 2) a high percentage of hematopoietic progenitors were transduced expressing ALD protein in long term ; 3) no early evidence of selective advantage of the transduced ALD cells nor clonal expansion were observed.

(This clinical trial is sponsored by Institut National de la Santa et de la Recherche Medicale and was conducted in part under a R&D collaboration with Cell Genesys, Inc., South San Francisco, CA)

Supported by grants from INSERM, the European Leukodystrophy Foundation, Association Francaise contre les Myopathies, Programme Hospitalier de Recherche Clinique of the Health Ministry (AOM 3043) and the European Union Project LSHM-CT-2004-502987.

The Stop ALD Foundation Supports and Attends The Symposium on X-linked Adrenoleukodystrophy and Adrenomyeloneuropathy - In Memoriam Dr. Hugo Wolfgang Moser

The following meeting was co-sponsored and attended by The Stop ALD Foundation and took place February 2008 in Boston.

Wednesday, 2/6/08

6:00 Reception at the Royal Sonesta Hotel
7:00 Dinner at Dante

Thursday, 2/7/08

7:30 Introduction and Welcome, Robert Brown
7:45 Tribute to Hugo W. Moser (1924 - 2007), Florian Eichler

Genetic and Molecular Pathophysiology of ALD and AMN
Moderator: Kenneth Fischbeck

8:00 Genetics of X-ALD, David Valle 
8:30 Modifier genes in X-ALD, Patrick Aubourg
8:45 Animal Models of ALD, Johannes Berger
9:15 Animal Models of AMN, Alex McCampbell
9:45 Axonal Degeneration in ALD, AMN and Related Disorders, Jack Griffin (tentative)

10:15-10:45 Discussion
10:45-11:00 Coffee

Metabolic Aspects of ALD and AMN 
Moderator: Florian Eichler

11:00 Biochemistry of X-ALD, Stephen Kemp
11:30 Cholesterol Deprivation in ALD, Marc Engelen 
12:00 Biophysical Properties of Very Long Chain Fatty Acids, Jim Hamilton

12:30-1:30 Lunch

1:30 Role of the Peroxisome in ALD and AMN, Steven Steinberg
2:00 Mitochondrial Dysfunction in ALD and AMN, Kirby Smith (tentative)

2:30-3:00 Discussion

Inflammatory Aspects of ALD
Moderator: Gilmore O'Neill

3:00 Microglial Apoptosis in ALD and AMN, Florian Eichler
3:30 Glycolipids, ALD and Autoimmunity, Ron Schnaar (tentative)

4:00-4:30 Coffee

4:30 Neurodegenerative Aspects of White Matter Disease, Bruce Trapp
5:00 Microglia in Experimental Models of Neurodegeneration, Joseph El Khoury

5:30-6:00 Discussion

7:00 Dinner

Friday, 2/8/08:

Therapeutic Strategies in ALD and AMN
Moderator: Ali Fatemi

8:00 Lorenzo's Oil in ALD and AMN, Gerald Raymond
8:30 Cell Based Therapies in ALD, Charles Peters 
9:00 Approaches to Gene Therapy of the CNS, Miguel Esteves
9:30 Gene Therapy in ALD and AMN, Nathalie Cartier

10:00-10:30 Discussion
10:30-11:00 Coffee

11:00 Immunomodulatory Strategies in MS, Samia Khoury
11:30 Modifiers of Oxidative Stress in ALD, Katherine Sims

12:00-12:30 Discussion

12:30 Lunch

European Society of Gene and Cell Therapy (ESGCT) The XVth Annual Congress of the European Society of Gene and Cell Therapy held in Rotterdam, The Netherlands, 27-30 October 2007

Kick-Off / Plenary Session: Presented Sunday, 28 October 2007 at ESGCT 2007 

Preliminary Data from the First Hematopoietic Stem Cell Gene Therapy Trial with Lentiviral Vector Demonstrate Expression of the Therapeutic Protein in High Percentage of Lymphocytes and Monocytes in Two Patients with X-Linked Adrenoleukodystrophy 

Nathalie Cartier1,2,3; Salima Hacein-Bey-Abina4,5; Gabor Veres6; Michel Vidaud1,7; Liliane Dal-Cortivo4,5; Laure Caccavelli4,5; Nizar Malhaoui8; Veronique Kiermer9,*; Denice Mittelstaedt9,; Andrew Simmons10; Cline Bellesme3; Francoise Audat4,5; Stephane Blanche8; Pierre Charnaud10; Muriel Audit11; Bruno Lohomme1,2,13; Jing- Chao Zhao- Emmonet1,2,13; Serge Fichelson14; Francoise Pflumio14; Anne Dubart-Kupperschmitt14; Rachel Salzman15; Amber Salzman16; Pierre Bougnores3; Alain Fischer5,8; Marina Cavazzana-Calvo4,5; Patrick Aubourg1,2,3 1 

INSERM U745, 2Faculty of Pharmacy, University Ren Descartes, and 3Department of Pediatric Endocrinology and Neurology, 13Hopital Saint-Vincent de Paul, Paris, France; 4Department of Biotherapies, 5U768, and 8Unit dImmunologie et Hematologie Pediatrique, Hopital Necker- Enfants Malades, Paris, France; 6Applied Genetic Technology Corporation, Alachua, FL, USA; 10R&D Development, 9Cell Genesys, Inc., South San Francisco, CA, USA; 11Institut Pasteur, CNRS-URA 3015, Paris, France; 12Gnthon, Evry, France; 14Department of Hematology, 
U567, Institut Cochin, Paris, France; 15The StopALD Foundation, Houston, TX, USA; 16The StopALD Foundation and GlaxoSmithKline, Philadelphia, PA, USA; *Present address: Nature Methods, New York, NY, USA; Present address: San Diego, CA, USA 

We report preliminary results in two children with cerebral X-linked adrenoleukodystrophy (ALD) who received in September 2006 and January 2007 hematopoietic stem cell (HSC) gene therapy using a HIV1-derived lentiviral vector. We have previously shown that the cerebral demyelination associated with cerebral ALD can be stopped or reversed within 18 months by allogeneic HSC transplantation. For the current HSC gene therapy procedure, mobilized peripheral blood CD34_ cells were transduced ex vivo for 18 hr with a non-replicative HIV1- derived lentiviral vector (provided by Cell Genesys, Inc.) expressing the ALD cDNA under the control of the MND promoter, and in the presence of Il-3, SCF, Flt3-ligand, MGDF, and CH-296 retro nectine. Transduced cells were frozen to perform replication-competent lentivirus (RCL) assays. After thawing and prior to reinjection, 50% and 30%, respectively, of transduced CD34_ cells expressed the ALD protein with a mean of 0.7 and 0.6 copies of integrated provirus/cell. Transduced CD34_ cells were infused to ALD patients after full myeloablation with cyclophosphamide and busulfan. 

Hematopoietic recovery occurred at day 15 post-transplant, and the procedure was uneventful. The percentage of corrected lymphocytes and monocytes in the peripheral blood of treated patients remained stable from day 30 to the last follow-ups. From 25% to 30% (Patient P1, 9 months after transplant) and 20% (Patient P2, 41/2 months after transplant) of CD14_, CD3_, CD19_, and CD3_CD56_ cells expressed the ALD protein (0.4 integrated provirus copy/cell). Tests assessing vector-derived RCL and vector mobilization were negative up to the last follow-ups. These early results support that: (1) ex vivo HSC gene therapy using HIV1-derived lentiviral vector is not associated with the emergence of RCL and vector mobilization; (2) a high percentage of hematopoietic progenitors were transduced expressing ALD protein in the short term; (3) no early evidence of selective advantage of the transduced ALD cells or clonal expansion was observed; and (4) HSC gene therapy appears to have short-term neurological effects comparable with allogeneic HSC transplantation. 

Sponsored by INSERM and conducted under an R&D collaboration with Cell Genesys, Inc., South San Francisco, CA.

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