FOXI3 haploinsufficiency contributes to low T-cell receptor excision circles and T-cell lymphopenia

• Published in: Journal of allergy and clinical immunology Vol. 150; no. 6; pp. 1556 - 1562
• Main Authors: Ghosh, Rajarshi, Bosticardo, Marita, Singh, Sunita, Similuk, Morgan, Delmonte, Ottavia M., Pala, Francesca, Peng, Christine, Jodarski, Colleen, Keller, Michael D., Chinn, Ivan K., Groves, Andrew K., Notarangelo, Luigi D., Walkiewicz, Magdalena A., Chinen, Javier, Bundy, Vanessa
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.12.2022
• Subjects: Child; FOXI3; Genomics; Humans; Infant, Newborn; Receptors, Antigen, T-Cell - genetics; T-cell lymphopenia; T-cell receptor excision circles; T-Lymphocytes; T-cell lymphopenia; CADD; TCR; FOXI3; TREC; ATO; TCL; NBS; T-cell receptor excision circles
• ISSN: 0091-6749; 1097-6825; 1097-6825
• DOI: 10.1016/j.jaci.2022.08.005

Newborn screening can identify neonatal T-cell lymphopenia through detection of a low number of copies of T-cell receptor excision circles in dried blood spots collected at birth. After a positive screening result, further diagnostic testing is required to determine whether the subject has severe combined immunodeficiency or other causes of T-cell lymphopenia. Even after thorough evaluation, approximately 15% of children with a positive result of newborn screening for T-cell receptor excision circles remain genetically undiagnosed. Identifying the underlying genetic etiology is necessary to guide subsequent clinical management and family planning. We sought to elucidate the genetic basis of patients with T-cell lymphopenia without an apparent genetic diagnosis. We used clinical genomic testing as well as functional and immunologic assays to identify and elucidate the genetic and mechanistic basis of T-cell lymphopenia. We report 2 unrelated individuals with nonsevere T-cell lymphopenia and abnormal T-cell receptor excision circles who harbor heterozygous loss-of-function variants in forkhead box I3 transcription factor (FOXI3). Our findings support the notion that haploinsufficiency of FOXI3 results in T-cell lymphopenia with variable expressivity and that FOXI3 may be a key modulator of thymus development.