1. Characterization of Infants with Idiopathic Transient and Persistent T Cell Lymphopenia Identified by Newborn Screening—a Single-Center Experience in New York State
- Author
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Artemio M. Jongco, Elise Hon, Catherine Capo, Robert Sporter, Shouling Zhang, Vincent R. Bonagura, D.W. Rosenthal, Brianne Navetta-Modrov, Omer Elshaigi, Foysal Daian, Emily Bae, and Amanda Innamorato
- Subjects
Male ,medicine.medical_specialty ,T-Lymphocytes ,T cell ,Immunology ,New York ,Single Center ,medicine.disease_cause ,Neonatal Screening ,Lymphopenia ,Internal medicine ,Rotavirus ,medicine ,Humans ,Immunology and Allergy ,Public Health Surveillance ,Lymphocyte Count ,Retrospective Studies ,Newborn screening ,T-cell receptor excision circles ,business.industry ,Viral Vaccine ,Vaccination ,Infant, Newborn ,Viral Vaccines ,CD4 Lymphocyte Count ,medicine.anatomical_structure ,Cohort ,Female ,Disease Susceptibility ,business ,CD8 - Abstract
Newborn screening (NBS) quantifies T cell receptor excision circles (TREC) and identifies infants with T cell lymphopenia (TCL). This study elucidates the demographics, laboratory characteristics, genetics, and clinical outcomes following live viral vaccine administration of term infants with transient or persistent idiopathic TCL. A single-center retrospective analysis was performed from September 2010 through June 2018. Laboratory variables were compared with Mann-Whitney tests. Correlations between initial TREC levels and T cell counts were determined by Spearman tests. Twenty-two transient and 21 persistent TCL infants were identified. Males comprised 68% of the transient and 52% of the persistent TCL cohorts. Whites comprised 23% of the transient and 29% of the persistent cohorts. Median initial TREC levels did not differ (66 vs. 60 TRECs/μL of blood, P = 0.58). The transient cohort had higher median initial CD3+ (2135 vs. 1169 cells/μL, P
- Published
- 2021