T Cell Receptor Excision Circle (TREC) Assay for Newborn Screening of SCID
Molecular Technology in Newborn Screening: SCID and...
Transcript of Molecular Technology in Newborn Screening: SCID and...
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Molecular Technology in Newborn Screening: SCID and Beyond
ARUP Seminar
Salt Lake City, Utah October 17, 2013
Mei Baker, M.D., FACMG
Associate Professor, Department of Pediatrics
Co-Director, NBS Laboratory at WSLH
University of Wisconsin School of Medicine and Public Health
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History of NBS Molecular Testing
• 1994
– Washington: hemoglobin second tier testing (Hb S, C, and E) by RELP
– Wisconsin: CFTR mutation analysis for F508del
• 1998
– New England: 2 GALT mutations (Q & N) by RFLP
• 1999
– New England: MCADD (c.985A>G) by RFLP
• 2005
– Wisconsin: MSUD (p.Y438N) by Tetra-primer ARMS-PCR
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History of NBS Molecular Testing
• 2006
– New York: Krabbe disease (3 polymorphisms & 5 mutations) by DNA sequencing
• 2008
– Wisconsin: TREC assay for SCID screening by Real-time PCR
• 1st use of molecular test as a primary test for population screen
• 2010
– 36 NBSPs in US use molecular testing for CF
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Severe Combined Immunodeficiency (SCID)
Then… Now…
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Severe Combined Immunodeficiency (SCID)
• Infections in first year of life – recurrent, etiology bacterial, viral and fungal – persistent despite routine treatment – severe--including sepsis, meningitis – opportunistic pathogens, such as PCP (pneumonia)
• Failure to thrive, chronic diarrhea • T cells decreased or absent
– poor proliferation in vitro to mitogens
• B cells absent or non-functional – low Ig’s after maternal IgG wanes; no specific antibody
responses
• Fatal without immune reconstitution
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Buckley Ann. Rev Imm 2004
SCID Genetic Analysis
• X-linked SCID is most common form (males)
• Specific gene defect can be found in 80% of cases (15 genes known)
• Clinical applications: – Carrier and
prenatal dx – Predict response
to BMT – Gene therapy
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Available Curative Treatment Modalities for SCID
• Bone Marrow Transplantation
• Gene Therapy (X-linked and adenosine deaminase deficiency SCID)
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Does SCID fulfill NBS criteria?
• Prevalence of the disease (1:100,000 or greater) – SCID: 1:66,000 (conservative estimate)
• Can the disorder be detected by routine physical exam? – SCID: No, SCID baby appears normal at birth.
• Does the disorder have a short asymptomatic period after birth? – SCID: Yes, SCID baby can be protected by passive maternal
immunity. • Does the disease cause serious medical complications?
– SCID: Yes, universally fatal within the first year of life • Is there potential for successful treatment?
– SCID: Yes, hematopoietic stem cell transplantation • Is there a confirmatory test?
– SCID: Yes, lymphocyte subpopulation analysis (flow cytometry) • Does early intervention leads better outcome?
– SCID: Yes! • Is there a screening test?
– SCID: Yes, measurement of TRECs using real-time qPCR
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SCID: Benefits of Early Diagnosis
0 2 4 6 8 1 0 1 2 1 4 1 6 1 8 2 0 2 2 2 4 0
1 0
2 0
3 0
4 0
5 0
6 0
7 0
8 0
9 0
1 0 0
Years post-transplantation
Perc
en
t su
rviv
ing
113 SCID infants with HSCT at greater than 3.5 months of age
66%
96% 46 SCID infants with HSCT at than 3.5 months of age or less
Buckley, R. JACI, 120 (4): 760-8 (2007)
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Screening for SCID in Newborns Considerations
•Many genes •Many mutations in each known gene •Some genotypes still not known
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TRECs are reduced in nearly ALL forms of SCID
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T-cell Generation in Newborns
• Two mechanisms: – Thymic output
– Postthymic T-cell proliferation
• Consequences: – Majority of T-cells are naïve T cells in newborns.
– TREC s are diluted out, and 10% T cells contain TRECs in newborns.
Schönland et al. Blood.2003; 102: 1428-1434
Gent et al, Clinical Immunology. 2009; 133: 95–107
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T Cell Receptor Recombination During Development in the Thymus
Generation of T cell receptor excision circles (TRECs) occur in >70% of all new (naïve) T
cells and can be detected by PCR
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NBS Card
(NSC) a.k.a. Guthrie Card
Dried blood
spots (DBS)
3 mm punch 96 well plate
Extract
DNA
Amplify TREC
by real-time
QPCR
Analyze
∆R
n
(am
plif
ica
tio
n
)
TREC plasmid
calibrators
ABI 7900HT Fast Real-Time PCR System
Overall Analysis Scheme
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Multiplexing _384-well Plate
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TREC Copy Numbers
Nu
mb
er
of
Infa
nts
Scre
en
ed
True Negatives
True
Positives
Normal Population
Affected
Cutoff Mean
(Affected)
Mean
(Normal)
False positives
False negatives
Affected Unaffected
Test Positive TP FP
Test Negative FN TN
Sensitivity = [TP] / [TP + FN]
Positive Predictive Value = [TP] / [TP + FP]
Specificity = [TN] / [TN + FP]
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Initial TREC assay
Full term ≥ 40
Preterm ≥ 25 Full term <40 Preterm <25
TREC & Actin Assay on 2 additional
punches
Full term: TREC < 30
Actin > 10,000
Normal
Screening Abnormal
Full term: TREC < 30
Actin < 10,000
Screening inconclusive
Preterm: TREC < 25
Actin > 10,000
Screening Abnormal
Preterm: TREC < 25
Actin < 10,000
Screening inconclusive
SCID Testing Algorithm
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SCID Reporting Algorithm
Full term screening Abnormal
Call out results to PCP
Call out results to clinical
consultants
Confirmatory Dx
Work up
Full term screening
inconclusive
Preterm screening
inconclusive
Preterm screening Abn.
Written report and request a repeating NBS
specimen
Written Report and recommending
repeat NBS following NICU procedure
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Confirmatory testing
• Flow cytometry lymphocyte subset enumeration for T , B and NK cell
quantitation
• Lymphocyte (T and/or B) proliferation tests
• Quantitative immunoglobulin assessment (IgG, IgA, IgM and IgE)
• HIV testing (to rule out secondary causes of T-cell
lymphopenia)
• Genetics testing
• Others: enzymes, Fluorescence in situ hybridization (FISH)
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Special Considerations • TREC copy numbers
– Measurement units – DNA extraction – Calibrators
• TREC assay platform
– Multiplexing vs. single target – 384-well vs. 96-well
• Automation
• QA/QC issues • Premature Newborns
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Wisconsin Experience (January 1, 2008– December 31, 2012)
Infants Screened: 340,037
– Premature (< 37 wks) 30,664
– Full term 309,373
Abnormal results: 246 – Premature (<37 wks) 147 (0.04%)
– Full term 99 (0.03%)
Inconclusive Results: 472 – Premature (<37 wks) 382 (0.11%)
– Full term 90 (0.03%)
Total number of flow cytometry referral: 108
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Wisconsin Experience (January 1, 2008– December 31, 2012)
Severe T cell Lymphopenia Cases
• Rac 2 mutation
• ADA SCID
• T-B-NK+ SCID
• T-B+NK+ (3)
• RAG 1 SCID
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Wisconsin Experience (January 1, 2008– December 31, 2012)
Other T cell Lymphopenia Cases
• Chromosomal abnormalities
22q11.2 deletion (11)
Trisomy 21
• Syndromes with T cell impairment
Jacobsen syndrome
Tar syndrome
Ectrodactyly ectodermic dysplasia
Ataxia Telangiectasia
• Idopathic T-cell lymphopenia
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Improving NBS for CF to Reduce Screening false positives
using Next Generation sequencing Technology
IRT
Limited CFTR mutations panel
Screening Positive
Screening Normal
One Mut.
One Mut.
CFTR2 147*
Two Mut.
Screening Positive
Screening Normal ??
Two Mut.
No Mut.
*Disease-causing mutations and mutations with varying
consequences. (Sosnay et al, Nature Genetics, 2013)
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Specific Aims
1. Establish a method of simultaneously detecting 162 CFTR mutations/gene variants using dried blood spot routine newborn screening specimens to create IRT/DNA/DNA CF screening opportunity.
2. Demonstrate that the three-tier IRT/DNA/DNA CF screening protocol would significantly reduce false positive screening results caused by identification of CF heterozygote carrier infants.
3. Demonstrate that it is cost effective to implement the three-tier IRT/DNA/DNA CF screening protocol into routine NBS for CF.
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MiSeqDx Cystic Fibrosis System
• 162 CFTR mutations/variants (IUO version*)
– 127 single nucleotide mutations/variants
– 32 insertion/deletion mutations
– 2 large deletions
– PolyTG/PolyT region
*Product is currently under FDA review.
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Isolate DNA Prepare Libraries
Pool Libraries
Sequence on MiSeqDx
Review Data
Cystic Fibrosis System Workflow
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Hybridization
Extension/Ligation
PCR amplification
PCR Primers Anneal
Sequencing Library Generation
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Replaced by DNA from DBS (25 – 50 ng)
Michael L. Metzker, Nature Review Genetics, 2010
Key Features: 1. Robust and logical work flow 2. 46 + 2 samples multiplexing
platform 3. Dual indexing identification 4. Immediate result w/o additional
informatics requirements
Genotyping-by-sequencing
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Funding Support for SCID
Jeffrey Modell Foundation
Children’s Hospital of Wisconsin
Wisconsin State Laboratory of Hygiene
Center for Disease Control and Prevention
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Funding Support for CF
The Legacy of Angels Foundation
Co-Funders: Paul and Sue Rosenau
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Acknowledgements
CHW/MCW Jack Routes, MD Bill Grossman, MD, PhD James Verbsky MD, PhD Trivikram Dasu, PhD
UWSMPH/WSLH Charles Brokopp, DrPH Daniel Kurtycz, MD Gary Hoffman, BS Michael Cogley, BS Lisa Berkan, MT(ASCP) Marcy Rowe, BS
DHS Murray Katcher, MD, PhD
NIAID Daniel Douek, PhD
CDC Robert Vogt, PhD Francis Lee, PhD
UWSMPH/Pediatrics
Christine Seroogy, MD
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Acknowledgements
• WSLH and SMPH at University of Wisconsin-Madison Philip Farrell, MD, PhD. (Co-PI) Anne Atkins, MPH
• Michigan: Kevin Cavanagh, PhD Samya Nasr, MD
• Minnesota: Mark McCann, MS
Warren Regelmann, MD
• Newborn Screening and Molecular Biology Branch, Centers for Disease Control and Prevention Suzanne Cordovado, PhD Marie Earley, PhD Carla Cuthbert, PhD