Literature DB >> 22068910

Newborn screening for severe combined immunodeficiency; the Wisconsin experience (2008-2011).

James W Verbsky1, Mei W Baker, William J Grossman, Mary Hintermeyer, Trivikram Dasu, Benedetta Bonacci, Sreelatha Reddy, David Margolis, James Casper, Miranda Gries, Ken Desantes, Gary L Hoffman, Charles D Brokopp, Christine M Seroogy, John M Routes.   

Abstract

Severe combined immunodeficiency is a life-threatening primary immune deficiency characterized by low numbers of naïve T cells. Early diagnosis and treatment of this disease decreases mortality. In 2008, Wisconsin began newborn screening of infants for severe combined immunodeficiency and other forms of T-cell lymphopenia by the T-cell receptor excision circle assay. In total, 207,696 infants were screened. Seventy-two infants had an abnormal assay. T-cell numbers were normal in 38 infants, abnormal in 33 infants, and not performed in one infant, giving a positive predictive value for T-cell lymphopenia of any cause of 45.83% and a specificity of 99.98%. Five infants with severe combined immunodeficiency/severe T-cell lymphopenia requiring hematopoietic stem cell transplantation or other therapy were detected. In summary, the T-cell receptor excision circle assay is a sensitive and specific test to identify infants with severe combined immunodeficiency and severe T-cell lymphopenia that leads to life-saving therapies such as hematopoietic stem cell transplantation prior to the acquisition of severe infections.

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Year:  2011        PMID: 22068910     DOI: 10.1007/s10875-011-9609-4

Source DB:  PubMed          Journal:  J Clin Immunol        ISSN: 0271-9142            Impact factor:   8.317


  12 in total

1.  Neonatal diagnosis of severe combined immunodeficiency leads to significantly improved survival outcome: the case for newborn screening.

Authors:  Lucinda Brown; Jinhua Xu-Bayford; Zoe Allwood; Mary Slatter; Andrew Cant; E Graham Davies; Paul Veys; Andrew R Gennery; H Bobby Gaspar
Journal:  Blood       Date:  2011-01-27       Impact factor: 22.113

2.  Implementing routine testing for severe combined immunodeficiency within Wisconsin's newborn screening program.

Authors:  Mei Wang Baker; Ronald H Laessig; Murray L Katcher; John M Routes; William J Grossman; James Verbsky; Daniel F Kurtycz; Charles D Brokopp
Journal:  Public Health Rep       Date:  2010 May-Jun       Impact factor: 2.792

3.  Human phagocyte defect caused by a Rac2 mutation detected by means of neonatal screening for T-cell lymphopenia.

Authors:  Deborah Accetta; Grant Syverson; Benedetta Bonacci; Sreelatha Reddy; Christine Bengtson; Jill Surfus; Ronald Harbeck; Anna Huttenlocher; William Grossman; John Routes; James Verbsky
Journal:  J Allergy Clin Immunol       Date:  2010-12-16       Impact factor: 10.793

4.  [Jacobsen's syndrome, thrombopenia and humoral immunodeficiency].

Authors:  N Sirvent; F Monpoux; F Pedeutour; M Fraye; P Philip; M Ticchioni; C Turc-Carel; R Mariani
Journal:  Arch Pediatr       Date:  1998-12       Impact factor: 1.180

5.  Statewide newborn screening for severe T-cell lymphopenia.

Authors:  John M Routes; William J Grossman; James Verbsky; Ronald H Laessig; Gary L Hoffman; Charles D Brokopp; Mei W Baker
Journal:  JAMA       Date:  2009-12-09       Impact factor: 56.272

Review 6.  Transplantation of hematopoietic stem cells in human severe combined immunodeficiency: longterm outcomes.

Authors:  Rebecca H Buckley
Journal:  Immunol Res       Date:  2011-04       Impact factor: 2.829

7.  Assessment of thymic output in adults after haematopoietic stem-cell transplantation and prediction of T-cell reconstitution.

Authors:  D C Douek; R A Vescio; M R Betts; J M Brenchley; B J Hill; L Zhang; J R Berenson; R H Collins; R A Koup
Journal:  Lancet       Date:  2000-05-27       Impact factor: 79.321

8.  Development of population-based newborn screening for severe combined immunodeficiency.

Authors:  Kee Chan; Jennifer M Puck
Journal:  J Allergy Clin Immunol       Date:  2005-02       Impact factor: 10.793

9.  Persistent low thymic activity and non-cardiac mortality in children with chromosome 22q11.2 microdeletion and partial DiGeorge syndrome.

Authors:  P Eberle; C Berger; S Junge; S Dougoud; E Valsangiacomo Büchel; M Riegel; A Schinzel; R Seger; T Güngör
Journal:  Clin Exp Immunol       Date:  2008-11-24       Impact factor: 4.330

10.  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

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  42 in total

Review 1.  History and current status of newborn screening for severe combined immunodeficiency.

Authors:  Antonia Kwan; Jennifer M Puck
Journal:  Semin Perinatol       Date:  2015-04-30       Impact factor: 3.300

Review 2.  Newborn screening for severe combined immunodeficiency and T-cell lymphopenia.

Authors:  Jennifer M Puck
Journal:  Immunol Rev       Date:  2019-01       Impact factor: 12.988

3.  Fiscal implications of newborn screening in the diagnosis of severe combined immunodeficiency.

Authors:  Catherine Kubiak; Soma Jyonouchi; Caroline Kuo; Maria Garcia-Lloret; Morna J Dorsey; John Sleasman; Arthur S Zbrozek; Elena E Perez
Journal:  J Allergy Clin Immunol Pract       Date:  2014-08-28

4.  Newborn Screening for Severe Combined Immunodeficiency: Analytic and Clinical Performance of the T Cell Receptor Excision Circle Assay in France (DEPISTREC Study).

Authors:  Marie A P Audrain; Alexandra J C Léger; Caroline A F Hémont; Sophie M Mirallié; David Cheillan; Marie G M Rimbert; Aurélie M-P Le Thuaut; Véronique A Sébille-Rivain; Aurore Prat; Enora M Q Pinel; Eléonore Divry; Cécile G L Dert; Maxime A G Fournier; Caroline J C Thomas
Journal:  J Clin Immunol       Date:  2018-09-24       Impact factor: 8.317

5.  Screening of neonatal UK dried blood spots using a duplex TREC screening assay.

Authors:  Stuart P Adams; Samina Rashid; Tharindu Premachandra; Katie Harvey; Adeboye Ifederu; Melanie C Wilson; H Bobby Gaspar
Journal:  J Clin Immunol       Date:  2014-02-28       Impact factor: 8.317

6.  Lessons for Sequencing from the Addition of Severe Combined Immunodeficiency to Newborn Screening Panels.

Authors:  Jennifer M Puck
Journal:  Hastings Cent Rep       Date:  2018-07       Impact factor: 2.683

7.  Cross-Sectional Survey on Newborn Screening in Wisconsin Amish and Mennonite Communities.

Authors:  Shelby Sieren; Meghan Grow; Matthew GoodSmith; Gretchen Spicer; James Deline; Qianqian Zhao; Mary J Lindstrom; Anne Bradford Harris; Angela M Rohan; Christine M Seroogy
Journal:  J Community Health       Date:  2016-04

8.  Novel mutation in TP63 associated with ectrodactyly ectodermal dysplasia and clefting syndrome and T cell lymphopenia.

Authors:  Philip F Giampietro; Mei W Baker; Monica J Basehore; Julie R Jones; Christine M Seroogy
Journal:  Am J Med Genet A       Date:  2013-04-23       Impact factor: 2.802

9.  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

10.  Terminal deletion of 11q with significant late-onset combined immune deficiency.

Authors:  Mikko Seppänen; Hannele Koillinen; Satu Mustjoki; Mölkänen Tomi; Kathleen E Sullivan
Journal:  J Clin Immunol       Date:  2014-01       Impact factor: 8.317

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