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477 three dimensional imaging of multiple AAV serotypemutant vector transductions in the non human primate brain by massively parallel sequencing

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477 Three Dimensional Imaging of Multiple AAV Serotype/Mutant Vector Transductions in the Non Human Primate Brain By Massively Parallel Sequencing Molecular Therapy Volume 23, Supplement 1, May 2015 C[.]

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Molecular Therapy Volume 23, Supplement 1, May 2015

Copyright © The American Society of Gene & Cell Therapy S189

Presidential symPosium

mutation in 3 pts), 8 pts (29%) had prior allogeneic stem cell transplant

(allo-SCT), and 22 pts (78%) had either primary refractory disease

or CR1 duration of <12 months Of the 28 pts, 27 pts were evaluable

for response At the time of 19-28z CAR T cell infusion, 14 of 27

evaluable pts had morphologic disease (>5% blasts in BM) and 13

pts had minimal residual disease (MRD) 24 of 27 pts (89%) were in

complete remission (CR) following the 19-28z CAR T cell infusion;

11 of these pts had morphologic disease at the time of T cell infusion,

and 13 pts had MRD 21 of 24 CR (88%) was MRD negative A

median time to CR was 22.5 days (range, 9-33) 10 pts successfully

underwent allo-HSCT following the 19-28z CAR T cell therapy

The median follow-up is 6 months (range, 1-38 months) with 15 pts

having at least 6 months of follow-up Responses appear durable with

12 pts remaining disease-free, including 7 pts without subsequent

allo-SCT Median OS of all pts is 8.5 months While none of the 13

pts with MRD at the time of T cell infusion developed significant

cytokine release syndrome (CRS), 5 of 15 pts with morphologic

disease developed severe CRS that required either vasopressors

or mechanical ventilation for hypoxia, successfully managed with

corticosteroid and/or IL-6R inhibitor

Conclusion: Treatment with 19-28z CAR T cells can induce a high

CR rate of 89% in these heavily pretreated adult pts with R/R ALL

regardless of the disease risk characteristics including Ph+ status,

age, pre-T cell disease burden, prior allo-SCT, and CR1 duration

While CRS can develop following T cell infusion, the risk of CRS

predictably correlates with the disease burden and can successfully be

managed with corticosteroid and/or IL-6R inhibitor These findings

support the use of 19-28z CAR T cells in adult pts with R/R ALL and

warrant a further investigation in a larger phase 2 trial

476 Clonal Tracking of Engineered

Hematopoiesis In Vivo in Humans By Insertional

Barcoding

Luca Biasco,1 Francesca Dionisio,1 Danilo Pellin,2 Serena Scala,1,3

Luca Basso Ricci,1 Samantha Scaramuzza,1 Cristina Baricordi,1

Andrea Calabria,1 Stefania Giannelli,1 Victor Neduva,4 David

J Dow,4 Eugenio Montini,1 Clelia Di Serio,2,3 Luigi Naldini,1

Alessandro Aiuti.1,3

1 San Raffaele Telethon Institute for Gene Therapy (TIGET), Milan,

Italy; 2 CUSSB, Univ Vita-Salute San Raffaele, Milan, Italy;

3 Univ Vita-Salute San Raffaele, Milan, Italy; 4 Molecular and

Cellular Technologies, GlaxoSmithKline, Stevenage Herts, United

Kingdom; 5 Univ degli studi Roma Tre, Rome, Italy.

Upon gene therapy (GT) for adenosine deaminase (ADA)

deficient-SCID and Wiskott-Aldrich Syndrome (WAS), gene-corrected

hematopoietic stem/progenitor cells (HSPC) generated a stable

genetically engineered hematopoietic system where each

vector-marked cell is univocally barcoded by a vector integration site (IS)

To study the dynamics of human hematopoietic system, we collected

by LAM-PCR+Illumina sequencing 28.539.414 sequence reads

corresponding to 89.373 IS tagging clones belonging to 13 different

cell types purified from the bone marrow and the peripheral blood

of 4 WAS patients up to 48 months after GT We firstly identified

identical IS shared among CD34+ progenitors, and mature Myeloid/

Lymphoid cells as markers of the real-time clonal output of

vector-marked HSPC clones in vivo We unraveled the nature and timing

of short, intermediate and long term HSPC output showing that

CD34+ clones active at 3-6 months after GT are not detectable at later

follow up Distinct waves of HSPC diversity were observed during

the first 6-9 months after GT reaching a homeostatic equilibrium

only by 12 months By unsupervised clustering of IS similarities

among lineages we unveiled diverse HSPC output towards lymphoid,

myeloid and megakaryo-erythroid cells showing hints of a NK cells

origin distinct from T and B cells We exploited IS similarities to

infere and test hematopoietic hierarchies by combining conditional probability distributions and static/dynamic graphical models of dependencies We also estimated by mark-recapture approaches that just few thousands clones (1185-2884) are responsible for the long-term maintenance of the whole genetically engineered hematopoietic system The ongoing analyses on IS collected from 7 distinct CD34+ subtypes isolated from GT patients will further increase HSPC tracking resolution To evaluate the preservation of activity

by transplanted HSPC we exploited data derived from the IS-based tracking of 4.845 clones in ADA-SCID patients performed for up to 6 years after GT We showed that identical IS are consistently detected

at multiple lineages level even several years after GT Strikingly,

by semi-quantitative PCRs on specific vector-genome junctions we tracked a fluctuating but consistent output of marked HSPC over

a period of 5 years without the manifestation of clonal quiescence phases Since gamma-retroviral vector used in this GT trial actively transduce only replicating cells, this provide the first evidence that HSPC, awaken from dormancy in vitro, can still retain in vivo long-term activity Overall our work constitute the first molecular tracking

of hematopoietic system in humans The information gathered are crucial for the design of therapeutic approaches for a broad spectrum

of hematological diseases and tumors

477 Three-Dimensional Imaging of Multiple AAV Serotype/Mutant Vector Transductions in the Non-Human Primate Brain By Massively Parallel Sequencing

Kei Adachi,1 Zheng Liu,1,2 Christopher D Kroenke,1,2 Gregory A Dissen,2 Sergio R Ojeda,2 Hiroyuki Nakai.1

1 Oregon Health and Science University, Portland, OR; 2 Oregon Health and Science University, Oregon National Primate Research Center, Beaverton, OR.

Global therapeutic gene delivery to the central nervous system (CNS) offers a promising approach to treat CNS diseases and preclinical studies using rodents have shown AAV9 as a potential candidate to achieve this goal However, recent work has highlighted the existence of nonhuman primate (NHP)-rodent differences in AAV vector biology and transduction profiles in the CNS after gene delivery, making imperative a more rigorous evaluation of various AAV serotype and capsid mutant vectors in NHPs It is of particular importance to understand how each AAV strain (serotype

or mutant) is distributed and transduces cells in the brain of a primate species closely related to humans when injected into the bloodstream or cerebrospinal fluids (CSF) Here we report a novel approach to generate three-dimensional (3D) vector transduction heat maps of more than one hundred of AAV strains in the rhesus monkey brain when vectors are delivered via the cisterna magna In this approach, we integrate the vector transduction data obtained by AAV Barcode-Seq (an Illumina sequencing-based high-throughput vector transduction analysis) into an MRI image To show proof-of-principle of the method, a barcoded-AAV library containing 145 different AAV strains was directly injected into CSF via the cisterna magna of three rhesus macaques (4x1012 vg/kg) and their brains were subjected to MRI analysis before collection of the organ 6 weeks post-injection Six mm-thick coronal sections of the brain were made and photographed, and the right half of each section slice was diced into

6 x 7 x 7 mm3 cubes using a matrix, generating more than 100 cubes from a cerebral hemisphere Total DNA was then extracted from each cube using an automated magnetic particle processor and subjected

to AAV Barcode-Seq analysis to determine transduction efficiency of each AAV strain in each cube by multiplexed Illumina sequencing The coordinates of each cube were determined by aligning the photo images of each coronal section to the corresponding MRI images using an image alignment algorithm This strategy allowed us to

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Molecular Therapy Volume 23, Supplement 1, May 2015 Copyright © The American Society of Gene & Cell Therapy

S190

Gene editinG and Gene ReGulation ii

create 3D heat maps showing distribution and transduction of each

AAV strain in the entire NHP brain A preliminary analysis using one

of the three monkeys revealed that AAV1 vector spreads globally and

transduces all brain regions including the cerebral cortex while the

distribution of AAV2 was limited locally Unexpectedly, we found

that many other serotypes and mutants transduced the NHP brain

better than AAV9 when delivered into CSF Thus, imaging of AAV

vector distribution and transduction throughout the NHP brain by AAV

Barcode-Seq combined with MRI provides a powerful approach to

comprehensively study AAV vector-mediated CNS gene delivery in

clinically relevant animal models Our results emphasize the large

difference in AAV distribution and transduction efficiency that exists

in the brain of higher primates compared to rodent models

478 Highly Efficient Targeted Gene Addition in

CD34+ Hematopoietic Stem/Progenitor Cells by

Combining ZFN mRNA and AAV6 Donor Delivery

Jianbin Wang,1 Colin M Exline,2 Josh DeClercq,1 Patrick Li,1

Philip D Gregory,1 Paula M Cannon,2 Michael C Holmes.1

1 Sangamo Biosciences Inc., Richmond, CA; 2 Molecular

Microbiology and Immunology, University of Southern California

Keck School of Medicine, Los Angeles, CA.

Zinc-finger nucleases (ZFNs) drive highly efficient genome editing

by generating a site-specific DNA double-strand break (DSB) at a

predetermined site in the genome Subsequent repair of this break

via the non-homologous end-joining (NHEJ) or homology-directed

repair (HDR) pathways results in targeted gene disruption or gene

correction/addition, respectively Hematopoietic stem/progenitor

cells (HSPC) are an important clinical target for gene therapy These

cells can be readily harvested from the subject, engineered using viral

vectors, and re-introduced back into the patient where they give rise

to all of the mature cells of the blood and immune system Thus the

ability to edit the genome of HSPCs could provide a corrective therapy

for a number of monogenic diseases However, achieving high levels

of editing by HDR may be significantly more challenging than gene

knockout by NHEJ Here we report that the combination of delivering

the ZFNs as mRNA and corrective donor DNA via a rAAV6 vector

can induce highly efficient targeted gene addition in CD34+ HSPCs

Using CCR5-specific ZFNs and donor DNA templates as a model

system we show that targeted addition of a novel restriction fragment

length polymorphism (RFLP) was consistently achieved at >15%,

while insertion of an eGFP expression cassette was achieved at >10%

of the CCR5 loci in mobilized CD34+ cells Furthermore, targeting

the AAVS1 “safe harbor” locus with a pair of AAVS1-specific ZFNs

(mRNA) and a RFLP donor (rAAV6) resulted in >30% of AAVS1

alleles specifically being edited to include the RFLP, suggesting this

genome editing approach to achieve highly efficient targeted gene

addition in CD34+ cells can be applied to different genetic loci Edited

HSPC undergo normal hematopoiesis in both in vitro differentiation

assays and during engraftment of NSG mice Using fetal liver derived

cells, editing of primitive and more committed CD34+ HSPC subsets

was observed at similar levels in HSPC CFU cultures, and by analysis

of sorted populations of treated HSPC, including LT-HSC, and

through the secondary transplantation of NSG mice

The use of ZFNs in combination with rAAV6 delivery of the donor

DNA provides a significant advance in genome editing that has great

potential for targeted correction of human disease-causing mutations

and permanent transgene addition in human CD34+ HSPC

Gene Editing and Gene Regulation II

479 ZFN-Mediated In Vivo Genome Editing Results in Supraphysiological Levels of Lysosomal Enzymes Deficient in Hunter and Hurler Syndrome and Gaucher Disease

Thomas Wechsler,1 Russel DeKelver,1 Michelle Rohde,1 Susan Tom,1 Scott Sproul,1 Leo Ou,2 Kanut Laoharawee,2 Kelly M Podetz-Pedersen,2 Chester B Whitley,2 Scott R McIvor,2 Philip D Gregory,1 Michael C Holmes.1

1 Sangamo BioSciences Inc., Richmond, CA; 2 Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN.

Lysosomal storage diseases (LSDs) represent a group of inherited metabolic disorders associated with mutations in genes encoding lysosomal enzymes leading to systemic accumulation of toxic storage materials Manifestations include organomegaly, skeletal dysplasias, cardiopulmonary obstruction, and severe neurologic impairment, often leading to death by age 10 Current LSD therapies include enzyme replacement therapy, substrate reduction therapy and hematopoietic stem cell transplant (HSCT) However, all of these therapies are expensive, incompletely effective, and HSCT is associated with significant risk of morbidity and mortality Due to the unmet need genome editing strategies are proposed to permanently modify patient cells by genetically complementing the LSD defect This is achieved by utilizing engineered zinc finger nucleases (ZFNs)

to introduce a DNA cut at the target locus, mediating integration of

a therapeutic LSD donor cDNA To ensure long-term expression of the transgenes in vivo we target the albumin locus as a “safe harbor”

in hepatocytes via co-delivery of the albumin ZFNs and LSD donors

by adeno-associated virus (AAV) This system exploits the high transcriptional activity of the native albumin enhancer/promoter; uses stably modified hepatocytes to potentially allow long-term expression of the inserted transgene; and utilizes an endogenous promoter obviating this requirement in the AAV payload We have previously exploited AAV-mediated in vivo targeting of the murine albumin “safe harbor” locus for the synthesis of therapeutic levels of FVIII and FIX to overcome the clotting defect in hemophilic mice Using the same approach, we co-delivered mouse albumin ZFNs with donor constructs encoding either human iduronate-2-sulfatase (IDS) deficient in Hunter syndrome, α-L-iduronidase (IDUA) for Hurler syndrome, or Glucocerebrosidase (GBA) for Gaucher disease via AAV in WT mice We show stable integration of the LSD donors

at the albumin locus, resulting in liver-specific expression and secretion of these proteins into plasma This led to a 4-fold (GBA), 10-fold (IDUA) or 100-fold (IDS) increase in enzymatic activity in the plasma, demonstrating that the secreted proteins are functional Importantly, increased activity was also detected in secondary tissues (spleen) showing efficient uptake and activity in distal tissues Moreover, preliminary data in MPSI and MPSII mice suggests these levels of IDS and IDUA expression may lead to correction of the enzyme deficiency IDS, IDUA and GBA expression remained stable throughout the study (up to 2 months), while expression of FIX has been stable for >1 yr suggesting this process results in long-term protein expression In summary, our data provide proof of concept for ZFN-mediated targeting of the albumin locus in hepatocytes as

an in vivo protein replacement platform to express different proteins associated with lysosomal storage diseases

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