Authors: | Guérin, A.; Kerner, G.; Marr, N.; Markle, J. G.; Fenollar, F.; Wong, N.; Boughorbel, S.; Avery, D. T.; Ma, C. S.; Bougarn, S.; Bouaziz, M.; Béziat, V.; Della Mina, E.; Oleaga-Quintas, C.; Lazarov, T.; Worley, L.; Nguyen, T.; Patin, E.; Deswarte, C.; Martinez-Barricarte, R.; Boucherit, S.; Ayral, X.; Edouard, S.; Boisson-Dupuis, S.; Rattina, V.; Bigio, B.; Vogt, G.; Geissmann, F.; Quintana-Murci, L.; Chaussabel, D.; Tangye, S. G.; Raoult, D.; Abel, L.; Bustamante, J.; Casanova, J. L. |
Article Title: | IRF4 haploinsufficiency in a family with Whipple's disease |
Abstract: | Most humans are exposed to Tropheryma whipplei (Tw). Whipple's disease (WD) strikes only a small minority of individuals infected with Tw (<0.01%), whereas asymptomatic chronic carriage is more common (<25%). We studied a multiplex kindred, containing four WD patients and five healthy Tw chronic carriers. We hypothesized that WD displays autosomal dominant (AD) inheritance, with age-dependent incomplete penetrance. We identified a single very rare non-synonymous mutation in the four patients: the private R98W variant of IRF4, a transcription factor involved in immunity. The five Tw carriers were younger, and also heterozygous for R98W. We found that R98W was loss-of-function, modified the transcriptome of heterozygous leukocytes following Tw stimulation, and was not dominant-negative. We also found that only six of the other 153 known non-synonymous IRF4 variants were loss-of-function. Finally, we found that IRF4 had evolved under purifying selection. AD IRF4 deficiency can underlie WD by haploinsufficiency, with age-dependent incomplete penetrance. |
Keywords: | innate immunity; t-cells; cell-differentiation; genetic-variants; herpes-simplex encephalitis; probe level; sequencing data; interferon regulatory factor-4; tropheryma-whipplei; inborn-errors |
Journal Title: | eLife |
Volume: | 7 |
ISSN: | 2050-084X |
Publisher: | eLife Sciences Publications Ltd. |
Date Published: | 2018-03-14 |
Start Page: | e32340 |
Language: | English |
ACCESSION: | WOS:000430674800001 |
DOI: | 10.7554/eLife.32340 |
PROVIDER: | wos |
PMCID: | PMC5915175 |
PUBMED: | 29537367 |
Notes: | Article -- Source: Wos |