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March 3, 2026Frontiers in Immunology3 citationsOpen Access

First 2-year experience of nationwide newborn screening for severe forms of T and B cell immunodeficiency: 2.3 million newborns analyzed using TREC and KREC in Russia

AMAndrey V. MarakhonovResearch Centre for Medical GeneticsAMAnna MukhinаResearch Centre for Medical GeneticsIEIrina EfimovaResearch Centre for Medical Genetics

Key Points

  • Identification of a broad spectrum of immunodeficiencies reduces the risk of severe infections and organ damage.
  • Timely intervention includes treatments such as hematopoietic stem cell transplantation and immunoglobulin replacement therapy.
  • Assessment involved a large-scale application of TREC and KREC testing across 2.3 million newborns in Russia.
  • Future improvements focus on enhancing protocols and individualized medical management for affected infants.

Abstract

Importantly, early diagnosis through NBS allowed for the timely initiation of disease-specific treatments, including hematopoietic stem cell transplantation (HSCT), immunoglobulin replacement therapy, and targeted immunosuppressive or supportive care strategies. Early intervention may reduce the risk of severe infections, improve neurodevelopmental outcomes, and prevent irreversible organ damage or malignancies in predisposed syndromes. Overall, our study demonstrates the effectiveness of large-scale implementation of TREC/KREC-based NBS in identifying a broad spectrum of immunodeficiencies and highlights future directions for improving NBS algorithms, follow-up protocols, and individualized medical management for affected infants.

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Cite This Study

Marakhonov et al. (2026) studied this question.

synapsesocial.com/papers/69a76791badf0bb9e87e1736https://doi.org/10.3389/fimmu.2026.1742811
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