Autosomal recessive HOXA3 deficiency causes congenital athymia and laryngeal malformation.
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История · было → стало
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Dinges Sarah S, Bosticardo Marita, Hirschfelder Anke, Pala Francesca, Kopp Johannes, Glaser Viktor, Gru Nhagen Johannes, Sangiorgio Giuseppe, Ehlers Lisa, Durek Pawel, Staudacher Olga, Völler Mirjam, Worth Austen, Kölsch Uwe, Golwala Zainab M, Unterwalder Nadine, Lankes Erwin, Schunck Karl-Ulrich, Heinrich Frederik, Amini Kayla, Loukogeorgakis Stavros, Howley Evey, Kenney Heather, Fischer Hendrik S, Weber Sven C, Blankenstein Oliver, Meisel Christian, Wendt Anke, Stachelscheid Harald, Kaindl Angela, Bu Hrer Christoph, Balázs Anita, Mashreghi Mir-Farzin, Polansky Julia K, Wagner Dimitrios L, Davies E Graham, Mall Marcus A, Kreins Alexandra Y, Notarangelo Luigi D, von Bernuth Horst
Аннотация
OBJECTIVE: We characterize the first human with HOXA3 deficiency and investigate the role of HOXA3 in immune system development.
METHODS: We performed clinical and immunological phenotyping, as well as genetic sequencing. A homozygous nonsense variant in HOXA3 was identified, and functionally validated including RT-PCR, western blot, assessment of transcriptional activity and intracellular localization of HOXA3. We report clinical management and course.
RESULTS: The homozygous HOXA3 nonsense variant generates a truncated protein with cytoplasmic retention and reduced transcriptional activity. The clinical phenotype includes craniofacial and cervical anomalies, severe laryngopharyngeal malformation with epiglottic hypoplasia causing dysphagia and aspiration, central breathing disorder, and thymus aplasia. T-cell maturation in artificial thymic organoids (ATO) and recovery after thymus transplantation establish the T-cell defect as non-hematopoietic.
CONCLUSION: Human HOXA3 has non-redundant roles for the development of larynx and thymus. HOXA3 deficiency is a novel, life-threatening multisystem disorder. It is the first human Homeobox-gene disease causing congenital athymia. These findings expand the diagnostic gene panel for patients with a SCID phenotype and indicate epiglottic hypoplasia as a new specific co-morbidity of congenital athymia.
KEY MESSAGES: Homeobox A3 (HOXA3) deficiency is a novel cause of congenital athymia, characterized by craniofacial and cervical anomalies, and life-threatening laryngeal malformation. Human HOXA3, unlike murine Hoxa3, may be redundant for parathyroid and thyroid gland development. The loss of the homeodomain causes cytoplasmic retention of the HOXA3 protein, leading to reduced transcriptional activity.
CAPSULE SUMMARY: We describe HOXA3 deficiency as the 8th genetically defined cause of congenital athymia, facilitating life-saving thymus transplantation for future patients. Life-threatening laryngeal malformations provide a clinical diagnostic clue for congenital athymia.