SCID newborn screening: seven-year performance and outcomes including T-cell lymphopenia in Catalonia (Spain)

Purpose: Severe combined immunodeficiency (SCID) can be detected at birth through T-cell receptor excision circles (TREC) analysis in dried blood spots. This study summarizes the results of the consolidated SCID newborn screening (NBS) program in Catalonia (Spain) during the first seven years of program implementation (2017-2023). Methods: Newborns were screened for SCID using the EnLite Neonatal TREC assay (cut-off: 20 copies/μL), with confirmatory immunological and genetic testing performed in screen-positive cases. Definitive SCID diagnosis was established according to PIDTC-2022 definitions, while final diagnostic classification followed the recommendations provided by Blom et al. Results: ) resulted in successful outcomes in the three remaining patients. Overall and event-free survival reached 88%. Median age at diagnosis was 9 days and median age at initiation of definitive therapy was 3 months. In addition to SCID cases, 53 newborns were diagnosed with non-SCID T-cell lymphopenia (1:7,939), including syndromic, idiopathic, and reversible forms. During follow-up, patients with idiopathic T-cell lymphopenia did not develop significant infectious or autoimmune complications, except for one case of autoimmune neutropenia. Thirty-three cases were classified as false positives (0.008%). Conclusions: The Catalonian SCID newborn screening program demonstrated high clinical effectiveness, enabling early definitive treatment and excellent survival outcomes with a low false-positive burden. In addition, systematic follow-up of non-SCID T-cell lymphopenia identified through SCID screening appears warranted. These findings support the sustainability and clinical value of universal SCID screening programs.