| Literature DB >> 33713249 |
Chai Teng Chear1, Revathy Nallusamy2, Kwai Cheng Chan2, Ratna Mohd Tap3, Mohd Farid Baharin1, Sharifah Nurul Husna Syed Yahya1, Prasobhan Bala Krishnan1, Saharuddin Bin Mohamad4,5, Adiratna Mat Ripen6.
Abstract
X-linked agammaglobulinemia is a rare primary immunodeficiency due to a BTK mutation. The patients are characteristically deficient in peripheral B cells and serum immunoglobulins. While they are susceptible to infections caused by bacteria, enteroviruses, and parasites, fungal infections are uncommon in XLA patients. Here, we report a boy of Malay ethnicity who suffered from recurrent upper respiratory tract infections and severe progressive necrotizing fasciitis caused by Saksenaea erythrospora. Immunological tests showed a B cell deficiency and hypogammaglobulinemia. Whole-exome sequencing identified a dinucleotide deletion (c.1580_1581del) in BTK, confirmed by Sanger sequencing and predicted to be disease causing by in silico functional prediction tools (Varsome and MutationTaster2) but was absent in the gnomAD database. This mutation resulted in a frameshift and premature termination (p.C527fs), which disrupted the protein structure. The mother was heterozygous at the mutation site, confirming her carrier status. Flow cytometric analysis of monocyte BTK expression showed it to be absent in the patient and bimodal in the mother. This study describes a novel BTK mutation in a defined hotspot and an atypical fungal phenotype in XLA. Further studies are required to understand the pathogenesis of fungal infection in XLA.Entities:
Keywords: BTK; Necrotizing fasciitis; Saksenaea erythrospora; X-linked agammaglobulinemia; mutation
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Year: 2021 PMID: 33713249 DOI: 10.1007/s10875-021-01017-3
Source DB: PubMed Journal: J Clin Immunol ISSN: 0271-9142 Impact factor: 8.317