| Literature DB >> 28694137 |
Stephanie Albin-Leeds1, Juliana Ochoa1, Harshna Mehta1, Beth H Vogel2, Michele Caggana2, Vincent Bonagura3, Heather Lehman4, Mark Ballow4, Arye Rubinstein5, Subhadra Siegel6, Leonard Weiner7, Geoffrey A Weinberg8, Charlotte Cunningham-Rundles9.
Abstract
Quantification of T-cell receptor excision circles (TRECs) for newborn screening for SCID has advanced the diagnosis of severe combined immune deficiency (SCID). However, it has led to the identification of infants with T cell lymphopenia without known cause. The clinical characteristics, appropriate laboratory monitoring, and outcomes of patients remain unclear. We performed a retrospective review of clinical and laboratory studies for 26 infants collected from 7 New York State referral centers from 2010 to 2016 with low TRECs (mean, 70copies/μl) and subnormal CD3 counts (mean, 1150/cubicmm). Over time absolute CD3 counts increased in 17 and decreased in 9; 22 (85%) have done well clinically regardless of absolute T cell values. Additional infants with TCL will continue to be identified in newborn screening panels. While most patients seem to do well clinically, parameters for diagnosis and monitoring have yet to be formalized, and additional information needs to be collected, causes and outcomes reported.Entities:
Keywords: Idiopathic T-cell lymphopenia; Newborn screening; Severe combined immunodeficiency; TREC level
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Year: 2017 PMID: 28694137 PMCID: PMC5736366 DOI: 10.1016/j.clim.2017.07.002
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969