SCID Screening: A New York State of Mind

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Transcript SCID Screening: A New York State of Mind

New York Newborn Screening Program - DNA
Jason Isabelle
June 4-5, 2012
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Severe Combined Immunodeficiency
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Caused by diverse mutations in several different genes
resulting in a combined immune deficiency
 X-Linked/Autosomal Recessive Inheritance
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Prevalence: ~1:40,000-100,000
 3-7 affected newborns in NY each year
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Extreme lack of T lymphocyte differentiation and function
 Severally impaired humoral/cellular immunity
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Often fatal within the first year of life
Prepared by Jason Isabelle-NYSNSP
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X-linked SCID
 Mutations in the gene encoding the common gamma chain
of IL-2,4,7, & 9 cytokine+ receptors
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Autosomal Recessive SCID
 Adenosine deaminase deficiency
 Jak3 tyrosine kinase deficiency
 RAG1,2
 IL-7R (α chain)
 CD-45
David Vetter: X-linked SCID
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Allogeneic hematopoietic stem cell transplant (HSCT)
 Donor marrow is depleted of T cells (Prevents GVHD)
 Allows for half-matched donor
 Climbing to a 90% success rate if administered <3 months of age
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Enzyme replacement therapy
 ADA deficient SCID
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Gene Therapy
 X-linked or ADA deficient SCID
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By-products of T cell receptor gene rearrangements during T
cell maturation in the thymus
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TRECs do not replicate during mitosis
 Episomal DNA that gets diluted by cell divisions
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TREC levels in peripheral blood reflect T cell production in the
thymus
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Low/No TRECs = Low/No T cell production by the thymus
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Created from the sequential rearrangements of the TCR α/δ
locus
 70% of thymocytes that express α/β TCR will form this specific TREC
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Signal joint region of this TREC is flanked by a conserved
region
 Allows for universal primer design that will always detect this TREC
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Occurs late in maturation
 Likely to generate a functional and diverse T cell repertoire
Hazenberg MD, Verschuren MCM,Hamann D, Miedema F, van Dongen JMJ (2001)
T cell receptor excision circles as markers for recent thymic emigrants: basic
aspects, technical approach, and guidelines for interpretation. J Mol Med 79:631640
Prepared by Jason Isabelle-NYSNSP

Automated assay developed and validated 12/2009-9/2010
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Submitted validation package to NYS Clinical Laboratory Evaluation
Program (CLEP) for approval on 9/08/2010
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CLEP and emergency regulation approved 9/27/2010
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SCID screening started 9/29/2010
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1st “True SCID” baby detected 12/27/2010 (NICHD Support)
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Presumptive Positive (Borderline) category added 1/25/2011
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Commissioner of Health officially adds SCID to NSP panel 4/12/2011
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CASM ‘Homebrew’ Extraction
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4 Solutions
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100μl Total Volume
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Tip Intensive
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Easily Scalable
 Low-Mid Throughput
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Average Yield: 4-5ng/μl
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RBC Lysis Solution
 Targets and destroys known PCR inhibitors
▪ Immunoglobulins, hemoglobin, etc
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Wash Solution
 Eliminate lysis by-products
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Buffer A
 Lyses of WBC’s and “scratches” fiber matrix
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Buffer B
 Neutralize pH and solubilize DNA
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Accommodate increased throughput
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Reduce repetitive stress injuries
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Address staffing shortages
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Increase reproducibility and consistency of
results
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Many manual processes are difficult to
automate
 Centrifugation, heating/cooling, vortexing, etc…
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Spot/Tip interactions
 10….960….3,840….11,520
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Labware Adjustments
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Liquid Type Editor
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Pipetting Template
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Volume Conditioning
METHOD CREATION
Each complete Liquid Handling System is capable of 1200 DNA extractions per 8 hour day.
Each Cytomat has a capacity of 6048 Tips when fully loaded.
Each Shaking Peltier Device can heat/cool from +4°C to +70°C .
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10 μl Final Volume
 (8μl Reaction Mix/2μl DNA)
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RNaseP/TREC Multiplex
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8-Point Standard Curve In Triplicate
 2000,1000,500,250,125,62.5,31.2,15.6 Copies
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+SCID/-SCID Control In Triplicate
 ADA, IL7R alpha, X-Linked, Omenn’s Syndrome—0 Avg
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Cutoff: 200 Trecs/μl of Whole Blood
Applied Biosystems
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Reporter/Quencher
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5’ Nuclease Activity
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Probe Cleavage
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Sequence Specific
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Multiplex Capability
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62bp amplicon
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Probe sequence spans signal joint
96 Well Extraction Plate to 384 Well Reaction Plate.
Shaking-Heating-Multiplate Adapters
Each 7900HT is capable of running 1500 samples per 8 hour day.
QPCR TERMS
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Baseline Adjustment
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Threshold Adjustment
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Algorithm Settings
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Individual Trace Analysis
Sample Passes
Applied Biosystems
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2nd most common form of SCID
 ~15% of all SCID cases
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Autosomal recessive inheritance
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Mutations in the ADA gene reduce or eliminate the
activity of the enzyme adenosine deaminase
 Toxic buildup of deoxyadenosine ensues
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Massive reduction in lymphocyte population
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Affected newborns have options
ADA
RNaseP
TREC
TREC AMPLIFICATION PLOT
RNASE P AMPLIFICATION PLOT
ADA
ADA
Dried Blood Spot Specimen
Multiplex PCR (TREC/RNaseP)
TREC ≥ 200
and
RNase P < WAL
TREC values are copies/ul RNaseP values are Cq
TREC< 200
Sample is retested in duplicate
RNase P ≥ 35
SCREEN NEGATIVE
Two of Three RNaseP WAL
AND
Two of Three TREC ≥ 200
OR
Average of Three TREC ≥200
SCREEN NEGATIVE
Two of Three RNaseP WAL
AND
Two of Three TREC < 200
AND
Average of Three TREC >125<200
AND
Gestation Age ≥37
AND
Has never been a PP before
PRESUMPTIVE POSITIVE
Two of Three RNaseP WAL
AND
Two of Three TREC <200
AND
Average of Three TREC <200
AND
Gestation Age <37
REPEAT PREMATURE
Two of Three RNaseP
WAL
AND
Two of Three TREC ≤200
AND
Gestation Age ≥37
AND
Average of Three TREC
≤200 if a previous PP
OR
Average of Three TREC
<150 if an initial
Specimen
REFERRAL
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Early detection benefits
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Adaptable screening methodology
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Prevalence
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Treatment
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Testing
Funding Support
The New York State Department of Health
The Eunice Kennedy Shriver Institute for Child Health
and Human Development
Jeffrey Modell Foundation