» Articles » PMID: 32166410

T-cell Receptor Excision Circles in Newborns with Heart Defects

Overview
Journal Pediatr Cardiol
Date 2020 Mar 14
PMID 32166410
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

In the fetus, the cardiac neural crest gives rise to both the thymus and the conotruncus of the heart. In newborn screening for severe T-cell lymphopenia neonates with congenital heart defects may be detected. In this study, we investigated the occurrence of T-cell lymphopenia in neonates with or without 22q11.2 deletion syndrome (del) suffering from heart defects. This retrospective cohort study included 125 patients with heart defects. T-cell receptor excision circles (TRECs), a measure for T-cell lymphopenia, were quantified by RT-PCR using stored newborn screening blood spots. Three patient groups were compared: non-conotruncal defects (n = 57), conotruncal defects (n = 42), and 22q11.2 del with conotruncal defects (n = 26). Significantly lower TREC values were detected in patients with 22q11.2 del and conotruncal heart defects compared to those with non-syndromic conotruncal (p < 0.001) and non-conotruncal (p < 0.001) defects. In contrast, no significant difference was found between patients with non-syndromic conotruncal and non-conotruncal heart defects (p = 0.152). Low TREC levels were obtained in neonates treated with heart surgery/intervention within 2 weeks after birth and in those with a fatal outcome (p = 0.02) independent of patient group. A correlation was found between low TREC numbers and oxygen saturation, SpO below 95% (p = 0.017). The SpO was significantly lower in the non-syndromic conotruncal group compared to non-conotruncal (p < 0.001) and 22q11.2 del group (p = 0.015). No correlation was found between low neonatal TRECs and infections needing hospitalization later in life (p = 0.135). Patients with 22q11.2 del and conotruncal defects have significantly lower TREC levels compared to patients with heart defects without this syndrome.

Citing Articles

Pre-Transplant Immunophenotyping in Pediatric Heart Transplant: A Role for the Immunologist?.

Gunderman L, Lancki N, Madden B, Ahmed A Pediatr Transplant. 2025; 29(2):e70052.

PMID: 39989346 PMC: 11848703. DOI: 10.1111/petr.70052.


Thymic Atrophy and Immune Dysregulation in Infants with Complex Congenital Heart Disease.

Bremer S, Boxnick A, Glau L, Biermann D, Joosse S, Thiele F J Clin Immunol. 2024; 44(3):69.

PMID: 38393459 PMC: 10891212. DOI: 10.1007/s10875-024-01662-4.


Positive Newborn Screening for Severe Combined Immunodeficiency: What Should the Pediatrician Do?.

Mongkonsritragoon W, Huang J, Fredrickson M, Seth D, Poowuttikul P Clin Med Insights Pediatr. 2023; 17:11795565231162839.

PMID: 37025258 PMC: 10071162. DOI: 10.1177/11795565231162839.


The Role of Zinc in the T-Cell Metabolism in Infection Requires Further Investigation - An Opinion.

Sergi C Front Immunol. 2022; 13:865504.

PMID: 35359968 PMC: 8960245. DOI: 10.3389/fimmu.2022.865504.


TREC Screening for WHIM Syndrome.

Evans 2nd M, Petersen M, Khojah A, Jyonouchi S, Edwardson G, Khan Y J Clin Immunol. 2021; 41(3):621-628.

PMID: 33415666 PMC: 7925426. DOI: 10.1007/s10875-020-00921-4.

References
1.
Haynes B, Markert M, Sempowski G, Patel D, Hale L . The role of the thymus in immune reconstitution in aging, bone marrow transplantation, and HIV-1 infection. Annu Rev Immunol. 2000; 18:529-60. DOI: 10.1146/annurev.immunol.18.1.529. View

2.
Hazenberg M, Otto S, Cohen Stuart J, Verschuren M, Borleffs J, Boucher C . Increased cell division but not thymic dysfunction rapidly affects the T-cell receptor excision circle content of the naive T cell population in HIV-1 infection. Nat Med. 2000; 6(9):1036-42. DOI: 10.1038/79549. View

3.
Chan K, Puck J . Development of population-based newborn screening for severe combined immunodeficiency. J Allergy Clin Immunol. 2005; 115(2):391-8. DOI: 10.1016/j.jaci.2004.10.012. View

4.
Raff H, Lee J, Widmaier E, Oaks M, Engeland W . Basal and adrenocorticotropin-stimulated corticosterone in the neonatal rat exposed to hypoxia from birth: modulation by chemical sympathectomy. Endocrinology. 2003; 145(1):79-86. DOI: 10.1210/en.2003-1130. View

5.
Ferencz C, NEILL C, Boughman J, Rubin J, Brenner J, PERRY L . Congenital cardiovascular malformations associated with chromosome abnormalities: an epidemiologic study. J Pediatr. 1989; 114(1):79-86. DOI: 10.1016/s0022-3476(89)80605-5. View