sickle cell disease: a crispr way to a cure · in sickle cell disease n about 100,000 americans...
TRANSCRIPT
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Sickle Cell Disease: A CRISPR way to a Cure
Fred Goldman MDDirector, Pediatric Blood and Marrow Transplant ProgramChildren�s of Alabama, University of Alabama, Birmingham
Advancements in the Care of Pediatric Cancer and Blood Disorders Symposium
November 20, 2018
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Disclosures
n GLG, Consultantn Karius, Scientific Advisory Board
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Outlinen Review sickle cell disease and therapiesn Review bone marrow transplant and gene
therapyn Discuss CRISPR technologyn Show preclinical datan Hurdles to overcome for FDA approval
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Sickle cell disease (SCD)n Most common genetic
disorder amongst African Americans
n Caused by a single base pair mutation in the beta-hemoglobin chain
ab
AAG
AAGTTC
Lys
ab
ab
Hgb A Hgb S Hgb C
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Pathophysiology in SCD
Endothelial injuryDecrease NO at vessel wallActivation of adhesion molecules
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Sickle cell carriers have some protective advantage from malaria
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Epidemiology and statisticsn The average life expectancy: 42 years for males and 48
years for femalesn Approximately 1 in 600 African American births results
in sickle cell diseasen About 100,000 Americans have sickle cell disease, 2000
new births annuallyn Nigeria, 90,000 born with SCD annuallyn This is a WORLD WIDE problemn 1000 children with SCD in Alabaman Newborn screening 50-60 new cases/yr in Alabama
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n Vasocclusive crises = pain crises¨ Sudden onset, begin early life¨ Bone infarctions¨ Extremities, sternum/rib¨ Dactylitis
¨ Management¨ Fluids¨ Analgesia
¨ Oral vs IV¨ Algorithms
Initial complications of SCD
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n Splenic sequestrationn Rapid increase in size of spleen from outflow obstructionn Anemia, reticulocytosis, thrombocytopenian Hypovolemian More prevalent in HbSCn Recurrentn Treatment
n Transfusionn Fluidsn Splenectomy for severe or recurrent events
n Aplastic crisisn Anemia with lack of RBC productionn Often caused by parvovirusn Anemia without reticulocytosisn Treatment
n Transfusion, slowlyn Fluids
Early complications of SCD
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n Acute chest syndromen Clinical definition
n CXR findingn Hypoxida/dyspnean Fever
n Causen Fat embolismn Infectionn Infarctionn Unknown
n Leading cause of deathn Treatment
n Transfusionn Oxygenn Fluidsn Incentive spirometryn Empiric antibiotics
Common complications of SCD
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n Avascular necrosisn Femoral and humeral heads
commonn Limited collateral circulationn Up to 30-50% of adults
n Biliary stone formationn Chronic hemolysis n Frequent cause of abdominal pain
and jaundicen 30-50% of patients develop by
adulthoodn Treat with cholecystectomy via
laparoscopic procedure
Common complications of SCD
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n Increased risk due to splenic dysfunctionn Encapsulated bacteria susceptibilityn Pneumococcus is leading cause of sepsis in SCD patientsn PCN prophylaxis in newborn till 5 yo
¨ Study by Gaston et al NEJM 1986n 13 of 110 positive infections on placebo armn 2 of 105 positive infections on penicillin arm
n Prevnar vaccination (13 valent)
Infectious complications of SCD
Halasa, CID 2007
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n Overt stroken 5-10% of HbSS patients prior
to 18yon Thrombotic or infarctive event
of large intracranial arteriesn Presents with weakness, aphasia,
seizures, LOCn Permanent neurological damage
and long-term disabilityn Silent stroke
n Most common neurologic injuryn 22% of children b/w 6-19 yon No overt clinical featuresn Increased T2 signal
abnormalities on MRI without corresponding deficits.
Neurologic complications of SCD
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n Treatment-acute¨ Exchange transfusion (preferred)¨ If Hb<10, could start with simple transfusion if time issue¨ Oxygen to keep sat >95%
n Long term management¨ SIT trial (DeBaun NEJM 2014)
n Randomized SCD 5-15 yo with silent stroke to receive regular blood transfusions or standard care (observation group).
n Transfusion 1/99 stroke Observation 7/96. Concluded transfusion better than observation for secondary prevention
¨ STOP trial-n For patients with abnormal TCD, transfusion is superior to no
therapy¨ TWITCH-
n Multicenter phase 3 trial showed HU was as good as transfusion to prevent stroke in children with abnormal TCD
Neurologic complications of SCD
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n Prevention of strokesn Transfusion
n Trans cranial Doppler (TCD) n Flow velocity of cerebral artery
Neurologic complications of SCD
Pegelow JPeds 1995STOP Trial- Adams NEJM 1998
Abnormal TCD pts
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Hydroxyurea therapy in SCDn Mechanism of action
¨ Increases Hgb F, lowers white blood cell count¨ Makes blood less “viscous” and white cells less sticky
¨ BABY HUG Trial¨ Randomized placebo control trial 2003-9 (~100 pts each group)¨ HgbSS age 1-2, received HU 20 mg/kg/d¨ Primary endpoint improvement in splenic or renal function
Wang et al, Lancet 2011
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Experimental therapies in SCD
n Anti-sickling agents ¨ Voxelotor (GBT440)
n Selectin inhibitors¨ Rivipansel (GMI 1070)
n Hgb F upregulators/inducers¨ Pomalidomide, HQK-1001
n NK T cell antibodies¨ IKTT
n Leukotriene antagonists¨ montelukast
n Anti-coagulants and anti-platelet agents¨ Heparin like molecules, NAC, aspirin
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Curative options in SCDn Hematopoietic Stem Cell Transplantation
n Allogeneicn Long standing track recordn Various donorsn Different conditioning
n Autologousn Experimentaln Gene correction/gene addition approaches
n Active clinical trials for lentiviral Hgb b n Active clinical trial for knocking down Bcl11a,
leading to increases in Hgb F????
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Bone marrow/PBSC harvested from donor
Myeloablativechemotherapy or serotherapy
Stem cell infusion
Prevention of GvHD and infection, immune system development
Baby with malignancy or “genetic disease”
Allogeneic HSCTCord blood donor
from NMDP registry
Day -8 to -1 Day 0 Day 1 to 120
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BoneMarrow
Cord Blood
Source of hematopoietic stem cells for transplant
Peripheral blood stem cells
CD34+
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Bone marrow/PBSC harvested from donor
Myeloablativechemotherapy or serotherapy
Stem cell infusion
Prevention of GvHD and infection, immune system development
Baby with malignancy or “genetic disease”
Allogeneic HSCT
Cord blood donor from NMDP
registry
Day -8 to -1 Day 0 Day 1 to 120
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Transplant preparative regimens
n Myeloablative conditioning (MIC)n Bu 16mg/kg + Cytoxan 200
mg/kgn Cytoxan 120 mg/kg + 1200 TBIn Blood counts drop out
completelyn Reduced intensity conditioning (RIC)
n Flu 150 mg/m2 + Melphalan 140 mg/m2 + CAMPATH
n counts drop but less toxicityn Non myeloablative conditioning (NIC)
n Flu 150 mg/m2 + 200 TBIn Counts may not drop, goal may
only be to achieve partial chimerism
Intensity
toxi
city
RICNIC MIC%
don
or c
him
eris
m
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Transplant phases and complications§ Pre/early engraftment
§ Hematopoietic recovery§ Transfusion dependent!!
§ Infections § Prophylaxis and treatment
strategies § Severe mucositis
§ Prevention and treatment strategies (KGF, pain medications)
§ Early tissue repair requires PMNs
§ Post engraftment (1-12 month)
§ Graft vs host disease§ Viral reactivation§ Immune reconstitution
0
100
0 15 30 60
HgbANCPlts
Days (post BMT)%
nor
mal
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Infection risks based on transplant phase
Mackall et al, BMT, 2009
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Transplant specific complication§ Acute graft vs host disease§ Manifest by rash, diarrhea,
increase LFTs§ Occurs within first 100 days
§ Chronic graft vs host disease
§ Occurs after 100 days§ Skin-dyspigmentation, leathery§ Mouth-leukoplakia§ Eyes-dry, itchy§ Joints- decreased ROM§ Liver- elevated Bili
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BMT for sickle cell diseasen Donor identification is a
problem ¨ 15% will have matched-sibling donor¨ 50% will have HLA-matched unrelated
donor (MUD)¨ >35% have no suitable MUD¨ 100% have haplo-identical family
member!
n Due to toxicities, BMT is reserved for those with severe disease¨ Some debate for those with
matched sibling donors!!
Human leukocyte antigen (HLA) typing
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Matched sib BMT for SCD
Walter et al, BBMT, 2016
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Type/year Transplant regimen
# ptsage
Alive without SCD
GVHDAcute/chronic
Death(cause)
Cord-related2016
Bu/CY/ATG 44(2-20)
38 3/0 4MOF, hem
Cord-MUD2014
Flu/Mel/CamBu/Flu/Cam
43(1-22)
20 13/4 14%MOF, infxn
MUD 2015 TT/TreoFlu/ATG//CsA-Mtx
6(27-48)
5 0/0 0
MUD 2016 Flu/Mel/Campath//CsA-Mtx-Pred
29(6-19)
19 8/11 8(GVHD)
MUD and cord transplant for SCD
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Haplo transplant for SCD
n Good data to daten Everyone has a donorn Short term follow-up
Referenceyear
Transplant regimen # ptsage
Alive w/o SCD
GVHDAcute/chronic
Death(cause)
H Bolanos-2012
Cy/Flu/TBI/ATGptCy/CsA/MMF
14(15-52)
8 0/0 0
H Dallas2013
Flu/Cy,TT,Bu/ATG/CD34+PBSC
8(4-17)
5 4/3 2 (GVHD)
H Saraf2018
ATG/Cy/Flu/TBIPBSC
8 7 2/1 1(?)
summary multiple 82(3-51)
60(73%)
13/8 9(multiple)
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Haplo protocol open at Children’s of Alabama CTN 1507
n Eligibility¨ Children aged 5-15
n History of overt stroke ischemia based on neuroimaging, or clinical evidence of permanent neurological injury lasting for 24 hours
¨ Adolescents and adults aged 15-46 withn History of two or more episodes of acute chest syndromen Transfusion dependent to prevent VOC complicationsn History of three or more severe VOC pain crises per year in
the 2-year period
HU -70 thru -10
ATG -9 thru -7TT (10 mg/kg) -7
Flu (30mg/m2) -6 thru -2
Cy (14.5mg/kg) -6 thru -5
TBI (2 Gy) -1
BM infusion
Cy (50 mg/kg) +4,+5
Siro +5MMF +5 thru +35
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• Introduction of new genetic material into the cells of an organism for therapeutic purposes
• Abnormal gene and normal functioning gene identified and cloned
• Cells responsible for disease are identified and accessible for manipulation
• A means of introducing and expressing genetic material (viral vector/gene editing)
• Over 2300 clinical gene therapy trials from 1989-2016 (per Wikipedia)
• 250 CAR T cell trials
Gene therapy
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Steps in ex-vivo gene-addition therapy
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Gene therapy for inherited disorders of the hematopoietic system
¨ Severe immune deficienciesn Common g chain ~50 ptsn ADA deficiency ~40 ptsn CGD ~ 5 ptsn WAS ~ 10 pts
¨ Marrow failure disordersn Fanconi�s anemia ~7 pts
¨ Hemoglobinopathiesn Sickle cell disease ~ 10 ptsn Thalassemia ~25 pts
¨ Metabolic storage disordersn Adrenoleukodystrophy ~ 30 ptsn MLD ~ 9 pts
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• 12 males with X-linked SCIDS• Bone marrow derived CD34+ HSC• Ex vivo expanded• transduced using retroviral vector
containing common g chain
Sustained Correction of X-Linked Severe Combined Immunodeficiency by ex Vivo Gene Therapy
Hacein-Bey-Abina et al, NEJM 2002
LMO2-Associated Clonal T Cell Proliferation in Two Patients after Gene Therapy for SCID-X1
Hacein-Bey-Abina et al, Science 2003
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BlueBird BioPhase 1/2 study HGB-206 for SCD:
n Eligibility-Severe SCD, age 18-35¨ 9 enrolled thus far
n CD34+ cells collected from patient¨ BM harvest (poor yields), now plerixafor mobilized PBSC
n Transduction with lentiglobin BB305 lentiviral vector and anti-sickling HgbAT87Q
¨ Poor efficiency and low vector copy numbern Myeloablation with full dose Busulfan
¨ Expected toxicities of fever, infection, cytopenia
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Kanter et al, ASH 2017
HSC collection
CD34 sortLentivirus transductionExpansionQuality control
Busulfan
Hospitalization
Hgb S quantificationTransfusion needs
BlueBird schema
myeloablative
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Issues with gene addition approach
n Failure to control integration sites¨ Random gene insertion in or near proto
oncogenes n Common gamma chain SCIDs 6/20n WAS trial 7/10n CGD 3/3
n Inefficiency/inconsistency of transductionn Variable numbers of gene modified cells
n Not under control of endogenous regulators
n VERY EXPENSIVE ($1,000,000/pt)
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Our approach vs others1. Patient population- who should we transplant?
A. Older age, adolescents/adultsB. Infants where disease-specific damage is minimal
2. Stem cell collection- how should we do this? A. Bone marrow harvest or plerixafor-mobilized HSCB. Cord blood
3. What is the best method for gene delivery with regards to safety, efficiency, cost? A. Gene addition, with LentivirusB. Gene editing with CRISPR/Cas9
4. How to safely prepare the patient with minimal toxicities and preservation of fertility?A. Full dose Busulfan myeloablationB. Mini-dose Busulfan
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UAB IRB approved protocol to collect HSCs from SCD patients
1. Bone marrow-SCD adult patients consent to bone marrow aspirate
2. Cord blood-sickle carrier moms at UAB OB agree to donate cord blood
3. PB HSC- SCD pediatric patients undergoing exchange transfusion, collect discarded blood anonymously
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Provides bacteria with innate immunity to defend against invading viruses
CRISPR-Cas System(Clustered Regularly Interspersed Palindromic Repeats)
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• The CRISPR/Cas system has been used for gene editing (adding, disrupting or changing the sequence of specific genes)
• By delivering the Cas9protein/enzyme and appropriate guide RNAs into a cell, the genome can be cut/repaired at any desired location
Gene correction via CRISPR/Cas
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CRISPR gene editingn Critical components
¨ guide RNA¨ modified recombinant Cas9¨ single stranded oligodeoxynucleotide
n Template for HR, 100 bp surrounds HgbA gene sequencing encompassing sickle mutation
n Nucleofection (electric shock)¨ Optimal settings to minimize cell death
n Cells need to be in “correct state”¨ S phase¨ Influence of culture conditions and cytokines used
Optimized concentration
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BFU-EGEMM
Differentiation in vitro of CRISPR/Cas modified sickle CD34+ bone marrow stem cells
n Purify CD34+ cells on immunomagnetic beads
n Nucleoporate with RNP/ssODN complex
n Plated onto methocultn Red blood cell precursor
colonies (single cell assay) are picked and DNA is sequenced
CD34+
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Mouse model of sickle cell disease
Science 245: 971-973 (1989)Science 318:1920-1923 (2007)
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Treosulfan conditioning permits engraftment and rescues the SCD phenotype
Devadasan et al, BBMT, 2018
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Our challenges for a phase 1 studyn HSC collection from sickle cell patients
¨ Plerixafor mobilization of children?¨ Coordinating cord blood collection of at risk infants
n Preparative therapy¨ Determining optimal Busulfan dose in children/infants
n Utilization of a GMP facility¨ Production scaled up
n Demonstrate efficacy and safety in murine and NSG mouse model for FDA approval¨ Transplant mice with “therapeutic dose”¨ Off target effects?
n Patient enrollment¨ Barriers to participation
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The first attempts to use a groundbreaking gene-editing technology1 in people will likely target patients with sickle cell disease2, a crippling inherited disorder that in the U.S. predominantly strikes African-Americans.That should be welcome news, after decades of sickle cell patients being neglected3 by the health care system, scientists, and drug companies. But the long and ugly history4 of unethical experimentation and mistreatment of black patients could make recruiting volunteers to try largely untested CRISPR therapies a tough sell.“You can’t expect this population is just going to stick out their arm for an IV,” said Mary Brown, who heads the Sickle Cell Disease Foundation of California and has worked with patients for four decades. “There’s a lot of education that needs to be done. I don’t want to say hand-holding, but that’s what it is.” A 2016 analysis of thousands of genomic studies showed what researchers called “persistent bias:” 81 percent of participants had European ancestry14, while people with African, Latin, or indigenous ancestry totaled less than 4 percent
HealthCRISPR could end sickle cell disease, but signing up black patients for clinical trials will be a hard sellBy Usha Lee McFarling @ushamcfarlingFebruary 21, 2018
DOXIMITY
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Comparison of transplant optionsAllogeneicMUD HSCT
AllogeneicHaplo HSCT
Allogeneic MRD HSCT
CurrentLentiHSCT
Proposed CRISPRHSCT
Donor available
40% 100% 15% 100% 100%
GVHD +++ +/++ + - -
Infection +++ +++ +++ ++ -/+
Reject risk ++ +++ + +++ ?
# done ~100 ~100 ~500 ~10 0
Cost ~ 600k ~ 600k ~ 400k low
Fertility Unlikely Unlikely Unlikely Unlikely probable
Chemo Hi dose Mid dose Mid dose Hi dose Lo dose
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Acknowledgements
n Tim Townes PhD ¨ Professor Biochemistry
UAB ¨ CEO Hemedits
n Townes lab ¨ Erik Westin¨ Lei Ding¨ Chao Li¨ Kevin Pawlik¨ Joe Sun¨ Jane Wu¨ Dewang Zhou¨ Divya Devadasan
n UAB¨ OB/GYN
n Spencer Kuper¨ Hematology service¨ GMP facility
n Larry Lamb
n Children’s of Alabama¨ Hematology health care
providersn All of our sickle cell
patients and their families