Vaccine development for Group A Streptococcus...Barnett M et al. JAMA 2014; Dallas A et al. Brit J...
Transcript of Vaccine development for Group A Streptococcus...Barnett M et al. JAMA 2014; Dallas A et al. Brit J...
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A/Prof Andrew Steer
Centre for International Child Health, University of Melbourne
Group A Streptococcal Research Group, Murdoch Children’s Research Institute, Melbourne
Department of General Medicine, Royal Children’s Hospital Melbourne, Australia
GVRIF Johannesburg March 2016
Vaccine development for Group A Streptococcus
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Outline
1. Pathogen and disease
2. The unmet need
3. Evidence for protective immunity
4. Vaccine candidate landscape
5. Vaccine development pipeline:
challenges and potential solutions
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Pathogen and disease
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The pathogen
A ubiquitous human pathogen
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Disease spectrum
Pharyngitis
Impetigo
Invasive disease
Acute glomerulonephritis
Acute rheumatic fever
Rheumatic heart disease
Scarlet fever
Toxic shock syndrome
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Rheumatic fever and rheumatic heart disease
Infectious disease Immune-mediated disease
Chronic non-communicable disease
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Disease spectrum
Tsoi et al. J Immunol Res 2015
Pharyngitis
Impetigo
Invasive
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Disease spectrum
Tsoi et al. J Immunol Res 2015
APSGN
ARF Rheumatic heart disease
Chronic kidney disease
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Burden of disease: Defining the unmet need
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Burden of disease
Pharyngitis
Impetigo
Invasive disease
Acute glomerulonephritis
Acute rheumatic fever
Rheumatic heart disease
615 million incident cases
162 million prevalent cases
660,000 incident cases
470,000 incident cases
470,000 incident cases
30 million cases
Carapetis JR, Steer AC, et al. Lancet Infect Dis 2005;5:685-94 Bowen et al. PLoS ONE 2015;10(8):0136789
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Rheumatic heart disease
~30 million patients
Infectious disease Immune-mediated disease
Chronic non-communicable disease
GBD figures 2013 courtesy David Watkins, U Washington
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Rheumatic heart disease
The REMEDY study Registry study of 3343 patients in 25 hospitals in Africa, India, Middle East Disease of young women -Median age 28 years -Two-thirds female A complicated and progressive chronic disease -Two-thirds with moderate-severe multi-valve disease -One-third with heart failure -One-quarter on oral anti-coagulation therapy
Zuhlke et al. Eur Heart J 2015
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Rheumatic heart disease
Case study: Fiji
-2619 patients over 5 years: 378 deaths (14%)
-2nd most common cause of death 5-29 years
Parks T, et al. PLOS NTD 2015
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Rheumatic heart disease
~30 million patients
~1 million with heart failure
~300,000 deaths p.a.
Infectious disease
GBD figures 2013 courtesy David Watkins, U Washington
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Burden of disease: mortality D
eath
s (1
00
0’s
)
Lozano et al. Lancet 2012
Rheumatic heart disease
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Invasive disease
USA 11,500 cases >1000 deaths
EU 15,000 cases 2400 deaths
High-income: 3-5 per 100,000 CFR: ~10-15%
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Severe community acquired sepsis (after introduction of Nm immunisation)
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Invasive disease
USA 11,500 cases 850 deaths
EU 15,000 cases 2400 deaths
High-income: 3-5 per 100,000 CFR: ~10-15%
? ?
?
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Kilifi: 1998 – 2011 Surveillance in children < 5 years: Incidence < 5 years: 35 per 100,000 Incidence < 1 year: 101 per 100,000 Incidence <28 days: 0.6 per 1000 (CFR 38%)
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Burden of disease: mortality D
eath
s (1
00
0’s
)
Lozano et al. Lancet 2012
Rheumatic heart disease
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Burden of disease: mortality
Rheumatic heart disease and invasive disease
Dea
ths
(10
00
’s)
Lozano et al. Lancet 2012 Carapetis, Mulholland, Steer, Weber Lancet ID 2005
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Pharyngitis
Shulman Clin Infect Dis 2012
Acute sore throat (USA) 15 million visits per year in adults & children 10-30% are caused by GAS GAS pharyngitis in children (USA) 10-15% of children per year $224 - 539 million per year
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Pharyngitis
Shulman Clin Infect Dis 2012
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Pharyngitis
Barnett M et al. JAMA 2014; Dallas A et al. Brit J GP 2015
72%
60%
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Pharyngitis
Barnett M et al. JAMA 2014
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40 million
25 million
Shapiro et al, JAC 2013
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Vaccine development: evidence
for protective immunity
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Evidence for protective immunity
Acquired natural immunity
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Evidence for protective immunity
Tsoi et al. J Immunol Res 2015
Pharyngitis
Impetigo
Invasive
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Evidence for protective immunity
AMA Am J Dis Child 1953;86:347-8
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Evidence for protective immunity
Acquired natural immunity
Extensive pre-clinical animal data
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Animal data
IP injection
Nasal challenge
Skin challenge
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Evidence for protective immunity
Acquired natural immunity
Extensive pre-clinical animal data
Human challenge model
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Evidence for protective immunity
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Evidence for protective immunity
Volunteers vaccinated
GAS vaccine type M1
n=19
Volunteers vaccinated
Placebo vaccine n=19
Throat painted
with GAS type M1
1 patient developed GAS pharyngitis*
9 patients developed GAS
pharyngitis
*Protective efficacy 89% p<0.01
Fox J Clin Invest 1973
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Can a vaccine prevent rheumatic heart disease?
Primary prevention
Infectious disease Immune-mediated disease
Chronic non-communicable disease
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Robertson et al BMC Cardiovasc Disord 2005
RR 0.20
Primary prevention
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*
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Can a vaccine prevent rheumatic heart disease?
Primary prevention
Infectious disease Immune-mediated disease
Chronic non-communicable disease
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Vaccine candidate landscape
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Vaccine candidate landscape
- 26-valent vaccine - 30-valent vaccine
VARIABLE REGION
CONSERVED REGION
Basis of M / emm typing (223 types)
Conserved between strains
- J8 vaccine - StreptInCor
Steer Curr Op Infect Dis 2009
M-based designs / non M-based candidates
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Vaccine candidate landscape
Non M-protein (active pre-clinical work)
– 4-antigen vaccine (“Combo”):
• CHO, SLO, SpyCEP, Spy0269
– Pilus
– SpeAB
– F7M5
– Spy469, spy1228, spy1801
– Spy7
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Vaccine candidate landscape
Non M-protein (status unclear) – Streptococcal C5a protease
– Fibronectin binding proteins
• Sfb1, Sfb2, SfbX, Protein F2, FbaB
• FbaA, Fbp54, GAPDH, shr
– GAS carbohydrate
– Platelet-Activating Factor Acetylhydrolase SsE
– Others
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26-valent vaccine (StreptAvax)
26-valent vaccine clinical trial -Based on 6-valent vaccine
-Adult volunteers
Safety
-Few systemic side effects
-No tissue cross-reactive antibodies
-No evidence of rheumatogenicity or nephritogenicity observed
Immunogenicity
-Post-vaccination serologic response (≥4- fold) to 20 of 26 epitopes
-Functional opsonic antibodies induced against all vaccine emm types
McNeil Clin Infect Dis 2005
*
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30-valent vaccine (StreptAnova) Protein 1
M1 3.1 M6.4 M2 M18 M28 M12 SPA M1
M4 M5.14 M11 M75 M19 M29 M14.3 M24 M4
M77 M22 M73 M89 M58 M44 M78 M118 M77
M83.1 M82 M81 M87 M49 M92 M114 M83.1
Protein 2
Protein 3
Protein 4
1-50 32-81 (1-25)2 (1-25)2 1-50 1-50 1-50 1-50 1-50
1-50 (1-25)2 1-50 1-50 (1-25)2 1-45 1-50 1-50 1-50
1-50 1-50 1-50 1-50 1-50 1-50 1-50 1-50 1-50
1-50 1-50 1-50 1-50 1-50 1-50 1-50 1-50
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30-valent vaccine (StreptAnova)
Phase I trial has completed enrolment
-Vaxent
-38 healthy volunteer adults enrolled (2:1 vaccine:comparator ratio)
-Schedule of 3 vaccinations over 6 months: 0, 30 and 180 days
-No initial safety issues
-Immunonogenicity available this year
-1 year safety follow-up
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J8 vaccine -Anti-J8 antibodies increase with age
-Animal studies:
-Stimulate production of opsonic antibodies
-Protect against IP challenge (parenteral vaccine)
-Protect against IN challenge (IN vaccine)
-Phase 1 trial (single dose): safe / immunogenic in 10 volunteers
-New preclinical data with S2 epitope of SpyCEP
Courtesy Prof Michael Good
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J8 vaccine
Pandey M et al, J Immunol 2016
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J8 vaccine
J8-Crm197 + S2-Crm197:
-adjuvanted with Alum for IM injection
-Australian and Canadian funding
-Phase I trial: multiple doses (x3)
J8-Liposomes.
-intranasal delivery
-IgA induction in mice
-Nasal challenge protection in mice.
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Vaccine development: StreptInCor
-Developed in Brazil
-55 amino acids of the C-terminus of M protein
-Immunogenic and protective in animal studies
-GMP production: PolyPeptide Group USA
-Formulation: Butantan Institute Brazil
-Scheduled to enter Phase I/IIa trials in 2016/17
Courtesy Prof Luiza Guilherme
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Vaccine development: clinical pipeline
M protein
– M protein type specific
• 26 valent vaccine
• 30 valent vaccine
– M protein conserved
• J8-DT
• J8-crm197 + S2-crm197
• StreptInCor
Phase I shortly to start
Phase I enrolment complete
Phase I/II completed
Phase I* completed
Phase I shortly to start
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Vaccine development: challenges
(and potential solutions)
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Challenges
Technical
1.Strain diversity
2.Standardisation of immunoassay
3.Animal model
4.Safety
Impeded pipeline
1.No consensus on PPC / TPP CDP
2.Limited engagement, limited investment
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Challenges
Technical
1.Strain diversity
2.Standardisation of immunoassay
3.Animal model
4.Safety
Impeded pipeline
1.No consensus on PPC / TPP CDP
2.Limited engagement, limited investment
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-Fiji studies: prospective surveillance >400 isolates 67 emm types
Steer AC et al, J Clin Microbiol 2009;47(8):2502–2509
1. Strain diversity multivalent vaccine
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Steer AC et al, Lancet Infect Dis 2009; 9(10):611-616
26-valent vaccine 2009 Study: >38,000 isolates from across the globe
% o
f is
ola
tes
incl
ud
ed in
vac
cin
e
0
10
20
30
40
50
60
70
80
90
100
HighIncome
countries
LatinAmerica
MiddleEast
Asia Africa Pacific
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26-valent 30-valent
30-valent vaccine: the solution?
-More than just addition of further M peptides
-Takes into consideration concept of “cross-opsonization”
Cross-protection experiments
-Bacterial antibodies evoked in rabbits by the 30-valent vaccine
-Antibodies kill both vaccine (VT) and non-vaccine (NVT) emm types
Dale et al, Vaccine 2011
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Total emm-types tested:
n=117 (30 VT, 87 NVT)
-VT and NVT: Over 50% killing = 99/117 (85%)
-Just NVT: Over 50% killing = 69/87 (79%)
Slide adapted from Prof Jim Dale
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30-valent vaccine
Dale et al Vaccine 2013
% Total isolates (cases)
VT only
VT + NVT
(cross-
opsonized)
Pharyngitis-US 98 98
Invasive Disease-US 90 93
Invasive Disease-Europe 78 97
Pharyngitis-Bamako 40 84
Pharyngitis-Cape Town 59 90
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Vaccine coverage
>1500 isolates
Regional representation
Clinical representation
All sequenced
All being evaluated for vaccine antigens +/-
Set of 150 core isolates available to developers
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Challenges
Technical
1.Strain diversity
2.Standardisation of immunoassay
3.Animal model
4.Safety
Impeded pipeline
1.No consensus on PPC / TPP CDP
2.Limited engagement, limited investment
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2. Immunoassay
David Goldblatt UCL -HL-60 assay for emm1 strain
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Challenges
Technical
1.Strain diversity
2.Standardisation of immunoassay
3.Animal model
4.Safety
Impeded pipeline
1.No consensus on PPC / TPP CDP
2.Limited engagement, limited investment
![Page 65: Vaccine development for Group A Streptococcus...Barnett M et al. JAMA 2014; Dallas A et al. Brit J GP 2015 72% 60% Pharyngitis Barnett M et al. JAMA 2014 40 million 25 million Shapiro](https://reader035.fdocuments.net/reader035/viewer/2022071105/5fdf95eb6adfd530f32e8928/html5/thumbnails/65.jpg)
3. Animal model
Alam F et al. PLoS ONE 2013
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Human challenge model of GAS infection MCRI 2017
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Challenges
Technical
1.Strain diversity
2.Standardisation of immunoassay
3.Animal model
4.Safety
Impeded pipeline
1.No consensus on PPC / TPP CDP
2.Limited engagement, limited investment
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4. Safety 21 children who had a sibling with
rheumatic fever
Purified M protein vaccine
Vaccinated weekly with increasing concentrations
For 18 – 33 weeks
Reduction in number of GAS infections 3* vaccinees developed rheumatic fever
Massell JAMA 1969;207:1115
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4. Safety
-Nature of Massell trial
-M protein vaccine studies not consistent
-Over 11,000 GAS vaccine recipients, no signal
-Naturally acquired M protein immunity does not cause ARF
-New M protein vaccines exclude “cross-reactive” sequences
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Challenges
Technical
1.Strain diversity
2.Standardisation of immunoassay
3.Animal model
4.Safety
Impeded pipeline
1.No consensus on PPC / TPP CDP
2.Limited engagement, limited investment
![Page 71: Vaccine development for Group A Streptococcus...Barnett M et al. JAMA 2014; Dallas A et al. Brit J GP 2015 72% 60% Pharyngitis Barnett M et al. JAMA 2014 40 million 25 million Shapiro](https://reader035.fdocuments.net/reader035/viewer/2022071105/5fdf95eb6adfd530f32e8928/html5/thumbnails/71.jpg)
1. TPP Clinical development plan
What is the indication?
Pharyngitis
Impetigo
Invasive disease
Acute glomerulonephritis
Acute rheumatic fever
Rheumatic heart disease
Scarlet fever
Toxic shock syndrome
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1. TPP Clinical development plan
Clinical development plans written:
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1. TPP Clinical development plan
Phase 1 – safety and tolerability in adults
Phase 2a – step-down dosing
Phase 2b – efficacy against pharyngitis (+/-impetigo)
Phase 3 – efficacy against pharyngitis (final lot)
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Challenges
Technical
1.Strain diversity
2.Standardisation of immunoassay
3.Animal model
4.Safety
Impeded pipeline
1.No consensus on PPC / TPP CDP
2.Limited engagement, limited investment
![Page 75: Vaccine development for Group A Streptococcus...Barnett M et al. JAMA 2014; Dallas A et al. Brit J GP 2015 72% 60% Pharyngitis Barnett M et al. JAMA 2014 40 million 25 million Shapiro](https://reader035.fdocuments.net/reader035/viewer/2022071105/5fdf95eb6adfd530f32e8928/html5/thumbnails/75.jpg)
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Vaccine development: pipeline
Very large burden of disease and unmet need
Vaccines in phase 1 or before, but none beyond
GAS vaccine investment 2014:
<$5 million
<0.1% of NTD global health funding
WHY?
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WHY?
No POC in humans?
Safety concerns?
No confidence
in candidates?
Lack of TPP / CDP?
Inadequate understand-
ing of biology?
Inadequate epi
Data?
Perception of the
market? HIC
LMIC
Complex trial
design?
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Vaccine development: pipeline
Pipeline strengths
-“Easy” read-out for initial phase III trials (pharyngitis)
-Prevent pharyngitis = prevent ARF and RHD
-Potential for role of human challenge
-CANVAS initiative*
-Global investment case: divide drivers*
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Vaccine development: pipeline
CANVAS (Coalition to Advance New Vaccines for GAS) -New Zealand and Australian governments -3-year funding period complete end 2016 -Three main areas: -1. Strain selection panel -2. Economic evaluation -3. Assay development -Next phase unclear
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Global investment case
High-income countries:
Prevent strep throat
Prevent invasive disease (incl. cellulitis)*
Reduce health care costs
Reduce antibiotic use
Low- and middle-income countries:
Prevent ARF/RHD
Prevent invasive disease
Reduce excess mortality
+/- impetigo & APSGN
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Global GAS vaccine consortium
Emerging consortium of interested partners:
-International Vaccine Institute
-Hilleman
-GSK Vaccines Institute for Global Health
-Others…
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Summary
-Very large burden of disease and need: HIC & LMIC
-HPV-like disease (RHD)
-Nm-like disease (IGAS)
-Potential to reduce AMR
-Vaccines in pipeline (but only few)
-Significant other work around vaccine trial readiness
-Levers are needed to advance development
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With thanks to
-Jim Dale, University of Tennessee, USA -Michael Good, Griffith University, Australia -Luiza Guilherme, Brazil -Allan Saul, GSK -David Kaslow, PD-VAC -Pierre Smeesters, Belgium -Jonathan Carapetis, Telethon Institute, Australia -John Fraser, Auckland University, NZ -Nicole Moreland, Auckland University, NZ -Kim Mulholland, MCRI, Australia -Florian Schodel, MedImmune Inc -Jeff Cannon, Telethon Institute, Australia
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Thank you