Literature DB >> 33607339

Ten Years of Newborn Screening for Severe Combined Immunodeficiency (SCID) in Massachusetts.

Jaime E Hale1, Craig D Platt2, Francisco A Bonilla3, Beverly N Hay4, John L Sullivan5, Alicia M Johnston6, Mark S Pasternack7, Paul E Hesterberg8, H Cody Meissner9, Ellen R Cooper10, Sara Barmettler11, Jocelyn R Farmer11, Donna Fisher12, Jolan E Walter13, Nancy J Yang11, Inderneel Sahai14, Roger B Eaton14, Alfred DeMaria15, Luigi D Notarangelo16, Sung-Yun Pai17, Anne Marie Comeau18.   

Abstract

BACKGROUND: Massachusetts began newborn screening (NBS) for severe combined immunodeficiency (SCID) using measurement of T-cell receptor excision circles (TRECs) from dried blood spots.
OBJECTIVE: We describe developments and outcomes from the first 10 years of this program (February 1, 2009, to January 31, 2019).
METHODS: TREC values, diagnostic, and outcome data from all patients screened for SCID were evaluated.
RESULTS: NBS of 720,038 infants prompted immunologic evaluation of 237 (0.03%). Of 237, 9 were diagnosed with SCID/leaky SCID (4% of referrals vs 0.001% general population). Another 7 were diagnosed with other combined immunodeficiencies, and 3 with athymia. SCID/leaky SCID incidence was approximately 1 in 80,000, whereas approximately 1 in 51,000 had severe T-cell lymphopenia for which definitive treatment was indicated. All patients with SCID/leaky SCID underwent hematopoietic cell transplant or gene therapy with 100% survival. One patient with athymia underwent successful thymus transplant. No known cases of SCID were missed. Compared with outcomes from the 10 years before SCID NBS, survival trended higher (9 of 9 vs 4 of 7), likely due to a lower rate of infection before treatment.
CONCLUSIONS: Our data support a single NBS testing-and-referral algorithm for all gestational ages. Despite lower median TREC values in premature infants, the majority for all ages are well above the TREC cutoff and the algorithm, which selects urgent (undetectable TREC) and repeatedly abnormal TREC values, minimizes referral. We also found that low naïve T-cell percentage is associated with a higher risk of SCID/CID, demonstrating the utility of memory/naïve T-cell phenotyping as part of follow-up flow cytometry.
Copyright © 2021 American Academy of Allergy, Asthma & Immunology. All rights reserved.

Entities:  

Keywords:  Athymia; Hematopoietic cell transplant (HCT); Newborn screening (NBS); Prematurity; SCID; TREC

Mesh:

Substances:

Year:  2021        PMID: 33607339      PMCID: PMC8113135          DOI: 10.1016/j.jaip.2021.02.006

Source DB:  PubMed          Journal:  J Allergy Clin Immunol Pract


  24 in total

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Authors:  Luigi D Notarangelo
Journal:  Curr Opin Pediatr       Date:  2014-12       Impact factor: 2.856

2.  SYK expression endows human ZAP70-deficient CD8 T cells with residual TCR signaling.

Authors:  Fabian Hauck; Britta Blumenthal; Sebastian Fuchs; Christelle Lenoir; Emmanuel Martin; Carsten Speckmann; Thomas Vraetz; Wilma Mannhardt-Laakmann; Nathalie Lambert; Marine Gil; Stephan Borte; Marie Audrain; Klaus Schwarz; Annick Lim; Wolfgang W Schamel; Alain Fischer; Stephan Ehl; Anne Rensing-Ehl; Capucine Picard; Sylvain Latour
Journal:  Clin Immunol       Date:  2015-07-14       Impact factor: 3.969

3.  SCID genotype and 6-month posttransplant CD4 count predict survival and immune recovery.

Authors:  Elie Haddad; Brent R Logan; Linda M Griffith; Rebecca H Buckley; Roberta E Parrott; Susan E Prockop; Trudy N Small; Jessica Chaisson; Christopher C Dvorak; Megan Murnane; Neena Kapoor; Hisham Abdel-Azim; Imelda C Hanson; Caridad Martinez; Jack J H Bleesing; Sharat Chandra; Angela R Smith; Matthew E Cavanaugh; Soma Jyonouchi; Kathleen E Sullivan; Lauri Burroughs; Suzanne Skoda-Smith; Ann E Haight; Audrey G Tumlin; Troy C Quigg; Candace Taylor; Blachy J Dávila Saldaña; Michael D Keller; Christine M Seroogy; Kenneth B Desantes; Aleksandra Petrovic; Jennifer W Leiding; David C Shyr; Hélène Decaluwe; Pierre Teira; Alfred P Gillio; Alan P Knutsen; Theodore B Moore; Morris Kletzel; John A Craddock; Victor Aquino; Jeffrey H Davis; Lolie C Yu; Geoffrey D E Cuvelier; Jeffrey J Bednarski; Frederick D Goldman; Elizabeth M Kang; Evan Shereck; Matthew H Porteus; James A Connelly; Thomas A Fleisher; Harry L Malech; William T Shearer; Paul Szabolcs; Monica S Thakar; Mark T Vander Lugt; Jennifer Heimall; Ziyan Yin; Michael A Pulsipher; Sung-Yun Pai; Donald B Kohn; Jennifer M Puck; Morton J Cowan; Richard J O'Reilly; Luigi D Notarangelo
Journal:  Blood       Date:  2018-08-28       Impact factor: 22.113

4.  Guidelines for implementation of population-based newborn screening for severe combined immunodeficiency.

Authors:  Anne Marie Comeau; Jaime E Hale; Sung-Yun Pai; Francisco A Bonilla; Luigi D Notarangelo; Mark S Pasternack; H Cody Meissner; Ellen Rae Cooper; Alfred DeMaria; Inderneel Sahai; Roger B Eaton
Journal:  J Inherit Metab Dis       Date:  2010-05-20       Impact factor: 4.982

5.  Newborn screening for SCID in New York State: experience from the first two years.

Authors:  Beth H Vogel; Vincent Bonagura; Geoffrey A Weinberg; Mark Ballow; Jason Isabelle; Lisa DiAntonio; April Parker; Allison Young; Charlotte Cunningham-Rundles; Chin-To Fong; Jocelyn Celestin; Heather Lehman; Arye Rubinstein; Subhadra Siegel; Leonard Weiner; Carlos Saavedra-Matiz; Denise M Kay; Michele Caggana
Journal:  J Clin Immunol       Date:  2014-03-01       Impact factor: 8.317

Review 6.  Applying public health strategies to primary immunodeficiency diseases: a potential approach to genetic disorders.

Authors:  Mary Lou Lindegren; Lisa Kobrynski; Sonja A Rasmussen; Cynthia A Moore; Scott D Grosse; Marsha Lynne Vanderford; Thomas J Spira; J Steven McDougal; Robert F Vogt; W Harry Hannon; Lisa V Kalman; Bin Chen; Marifran Mattson; Timothy G Baker; Muin Khoury
Journal:  MMWR Recomm Rep       Date:  2004-01-16

7.  Development of a routine newborn screening protocol for severe combined immunodeficiency.

Authors:  Mei W Baker; William J Grossman; Ronald H Laessig; Gary L Hoffman; Charles D Brokopp; Daniel F Kurtycz; Michael F Cogley; Thomas J Litsheim; Murray L Katcher; John M Routes
Journal:  J Allergy Clin Immunol       Date:  2009-05-31       Impact factor: 10.793

8.  Whole-exome sequencing identifies tetratricopeptide repeat domain 7A (TTC7A) mutations for combined immunodeficiency with intestinal atresias.

Authors:  Rui Chen; Silvia Giliani; Gaetana Lanzi; George I Mias; Silvia Lonardi; Kerry Dobbs; John Manis; Hogune Im; Jennifer E Gallagher; Douglas H Phanstiel; Ghia Euskirchen; Philippe Lacroute; Keith Bettinger; Daniele Moratto; Katja Weinacht; Davide Montin; Eleonora Gallo; Giovanna Mangili; Fulvio Porta; Lucia D Notarangelo; Stefania Pedretti; Waleed Al-Herz; Wasmi Alfahdli; Anne Marie Comeau; Russell S Traister; Sung-Yun Pai; Graziella Carella; Fabio Facchetti; Kari C Nadeau; Michael Snyder; Luigi D Notarangelo
Journal:  J Allergy Clin Immunol       Date:  2013-07-04       Impact factor: 14.290

9.  Retrospective TREC testing of newborns with Severe Combined Immunodeficiency and other primary immunodeficiency diseases.

Authors:  O Jilkina; J R Thompson; L Kwan; P Van Caeseele; C Rockman-Greenberg; M L Schroeder
Journal:  Mol Genet Metab Rep       Date:  2014-08-07

Review 10.  Salivary Cortisol Reactivity in Preterm Infants in Neonatal Intensive Care: An Integrative Review.

Authors:  Evalotte Mörelius; Hong-Gu He; Shefaly Shorey
Journal:  Int J Environ Res Public Health       Date:  2016-03-18       Impact factor: 3.390

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Review 1.  Future of Therapy for Inborn Errors of Immunity.

Authors:  Elena Perez
Journal:  Clin Rev Allergy Immunol       Date:  2022-01-12       Impact factor: 10.817

2.  Immunological Findings and Clinical Outcomes of Infants With Positive Newborn Screening for Severe Combined Immunodeficiency From a Tertiary Care Center in the U.S.

Authors:  Vasudha Mantravadi; Jeffrey J Bednarski; Michelle A Ritter; Hongjie Gu; Ana L Kolicheski; Caroline Horner; Megan A Cooper; Maleewan Kitcharoensakkul
Journal:  Front Immunol       Date:  2021-09-03       Impact factor: 7.561

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