Whole-exome Sequencing for the Identification of Rare Variants in Primary Immunodeficiency Genes in Children With Sepsis: A Prospective, Population-based Cohort Study. (18th March 2020)

• Record Type: Journal Article
• Authors: Borghesi, Alessandro; Trück, Johannes; Asgari, Samira; Sancho-Shimizu, Vanessa; Agyeman, Philipp K A; Bellos, Evangelos; Giannoni, Eric; Stocker, Martin; Posfay-Barbe, Klara M; Heininger, Ulrich; Bernhard-Stirnemann, Sara; Niederer-Loher, Anita; Kahlert, Christian R; Natalucci, Giancarlo; Relly, Christa; Riedel, Thomas; Kuehni, Claudia E; Thorball, Christian W; Chaturvedi, Nimisha; Martinon-Torres, Federico; Kuijpers, Taco W; Coin, Lachlan; Wright, Victoria; Herberg, Jethro; Levin, Michael; Aebi, Christoph; Berger, Christoph; Fellay, Jacques; Schlapbach, Luregn J
• Is Part Of: Clinical infectious diseases. Volume 71:Number 10(2020)
• Page Start: e614
• Page End: e623
• Publication Date: 2020-03-18
• Subjects: child -- exome sequencing -- genomics -- immunodeficiency -- sepsis -- variant -- variants of uncertain significance; Communicable diseases -- Periodicals; 616.905
• DOI: 10.1093/cid/ciaa290
• Languages: English
• ISSNs: 1058-4838

Abstract

Abstract: Background: The role of primary immunodeficiencies (PID) in susceptibility to sepsis remains unknown. It is unclear whether children with sepsis benefit from genetic investigations. We hypothesized that sepsis may represent the first manifestation of underlying PID. We applied whole-exome sequencing (WES) to a national cohort of children with sepsis to identify rare, predicted pathogenic variants in PID genes. Methods: We conducted a multicenter, population-based, prospective study including previously healthy children aged ≥28 days and <17 years admitted with blood culture-proven sepsis. Using a stringent variant filtering procedure, analysis of WES data was restricted to rare, predicted pathogenic variants in 240 PID genes for which increased susceptibility to bacterial infection has been reported. Results: There were 176 children presenting with 185 sepsis episodes who underwent WES (median age, 52 months; interquartile range, 15.4–126.4). There were 41 unique predicted pathogenic PID variants (1 homozygous, 5 hemizygous, and 35 heterozygous) found in 35/176 (20%) patients, including 3/176 (2%) patients carrying variants that were previously reported to lead to PID. The variants occurred in PID genes across all 8 PID categories, as defined by the International Union of Immunological Societies. We did not observe a significant correlation between clinical or laboratory characteristics of patients and the presence or absence of PID variants. Conclusions: Applying WES to a population-based cohort of previously healthy children with bacterial sepsis detected variants of uncertain significance in PID genes in 1 out of 5 children. Future studies need to investigate the functional relevance of these variants to determine whether variants in PID genes contribute to pediatric sepsis susceptibility. Abstract : In this population-based cohort, whole-exome sequencing identified known and unknown, rare, predicted pathogenic variants in primary immunodeficiency genes in 1 of 5 children with proven sepsis. Future studies need to validate whether these variants contribute to sepsis susceptibility.