| Literature DB >> 32681206 |
Connie H Lin1, Hye Sun Kuehn2, Timothy J Thauland1, Christine M Lee3, Suk See De Ravin4, Harry L Malech4, Timothy J Keyes5, Astraea Jager5, Kara L Davis5, Maria I Garcia-Lloret1, Sergio D Rosenzweig2, Manish J Butte6.
Abstract
We report the case of a patient with X-linked severe combined immunodeficiency (X-SCID) who survived for over 20 years without hematopoietic stem cell transplantation (HSCT) because of a somatic reversion mutation. An important feature of this rare case included the strategy to validate the pathogenicity of a variant of the IL2RG gene when the T and B cell lineages comprised only revertant cells. We studied the X-inactivation of sorted T cells from the mother to show that the pathogenic variant was indeed the cause of his SCID. One interesting feature was a progressive loss of B cells over 20 years. CyTOF (cytometry time of flight) analysis of bone marrow offered a potential explanation of the B cell failure, with expansions of progenitor populations that suggest a developmental block. Another interesting feature was that the patient bore extensive granulomatous disease and skin cancers that contained T cells, despite severe T cell lymphopenia in the blood. Finally, the patient had a few hundred T cells on presentation but his TCRs comprised a very limited repertoire, supporting the important conclusion that repertoire size trumps numbers of T cells.Entities:
Keywords: B cells; IL2RG; SCID; T cells; somatic reversion
Year: 2020 PMID: 32681206 PMCID: PMC7508923 DOI: 10.1007/s10875-020-00825-3
Source DB: PubMed Journal: J Clin Immunol ISSN: 0271-9142 Impact factor: 8.317