[A first pilot study on the neonatal screening of primary immunodeficiencies in Spain: TRECS and KRECS identify severe T- and B-cell lymphopenia]

An Pediatr (Barc). 2014 Nov;81(5):310-7. doi: 10.1016/j.anpedi.2014.08.002. Epub 2014 Sep 30.
[Article in Spanish]

Abstract

Introduction: Early diagnosis of primary immunodeficiency such as severe combined immunodeficiency (SCID) and X-linked agammaglobulinemia (XLA) improves outcome of affected infants/children. The measurement of T-cell receptor excision circles (TRECS) and kappa-deleting recombination excision circles (KRECS) can identify neonates with severe T or B-cell lymphopenia.

Objectives: To determine TRECS and KRECS levels from prospectively collected dried blood spot samples (DBS) and to correctly identify severe T and B-cell lymphopenia.

Material and methods: Determination of TRECS and KRECS by multiplex PCR from neonates born in two tertiary hospitals in Seville between February 2014 and May 2014. PCR cut-off levels: TRECS<15 copies/μl, KRECS<10 copies/μl, ACTB (β-actin)>1000 copies/μl. Internal (XLA, ataxia telangiectasia) and external (SCID) controls were included.

Results: A total of 1068 out of 1088 neonates (mean GA 39 weeks (38-40) and BW 3238g (2930-3520) were enrolled in the study. Mean (median, min/max) copies/μl, were as follows: TRECS 145 (132, 8/503), KRECS 82 (71, 7/381), and ACTB 2838 (2763, 284/7710). Twenty samples (1.87%) were insufficient. Resampling was needed in one neonate (0.09%), subsequently giving a normal result. When using lower cut-offs (TRECS<8 and KRECS<4 copies/μl), all the samples tested were normal and the internal and external controls were correctly identified.

Conclusion: This is the first prospective pilot study in Spain using TRECS/KRECS/ACTB-assay, describing the experience and applicability of this method to identify severe lymphopenias. The ideal cut-off remains to be established in our population. Quality of sampling, storage and preparation need to be further improved.

Keywords: Agammaglobulinemia ligada al cromosoma C; Cribado neonatal; Inmunodeficiencia combinada grave; Inmunodeficiencias primarias; Linfopenia; Lymphopenia; Newborn screening; Primary immunodeficiency diseases; Severe combined immunodeficiency; X-linked agammaglobulinaemia.

Publication types

  • Observational Study

MeSH terms

  • Agammaglobulinemia / blood
  • Agammaglobulinemia / diagnosis*
  • Agammaglobulinemia / genetics*
  • Algorithms
  • B-Lymphocytes
  • DNA, Circular / blood
  • Genetic Diseases, X-Linked / blood
  • Genetic Diseases, X-Linked / diagnosis*
  • Genetic Diseases, X-Linked / genetics*
  • Humans
  • Infant, Newborn
  • Longitudinal Studies
  • Lymphopenia / diagnosis*
  • Neonatal Screening / methods*
  • Pilot Projects
  • Prospective Studies
  • Severe Combined Immunodeficiency / blood
  • Severe Combined Immunodeficiency / diagnosis*
  • Severe Combined Immunodeficiency / genetics*
  • Severity of Illness Index
  • Spain
  • T-Lymphocytes

Substances

  • DNA, Circular

Supplementary concepts

  • Bruton type agammaglobulinemia