FOXN1 deficient nude severe combined immunodeficiency

Abstract

Nude severe combined immunodeficiency is a rare inherited disease caused by autosomal recessive loss-of-function mutations in FOXN1. This gene encodes a transcription factor essential for the development of the thymus, the primary lymphoid organ that supports T-cell development and selection. To date nine cases have been reported presenting with the clinical triad of absent thymus resulting in severe T-cell immunodeficiency, congenital alopecia universalis and nail dystrophy. Diagnosis relies on testing for FOXN1 mutations, which allows genetic counselling and guides therapeutic management. Options for treating the underlying immune deficiency include HLA-matched genoidentical haematopoietic cell transplantation containing mature donor T-cells or thymus tissue transplantation. Experience from other severe combined immune deficiency syndromes suggests that early diagnosis, supportive care and definitive management result in better patient outcomes. Without these the prognosis is poor due to early-onset life threatening infections.

Keywords: Alopecia; FOXN1; Immunodeficiency; Nail dystrophy; T-cell; Thymus.

Fig. 1

FOXN1 secondary/domain structure annotated with locations of mutations known to cause nude SCID in humans. The scale bar represents position in base pairs within the cDNA sequence. Also included is a bar chart showing number of cases described for each mutation