- Meeting abstract
- Open Access
OR7-002 – Pyrin 577 mutations in dominant autoinflammation
© Stoffels et al; licensee BioMed Central Ltd. 2013
- Published: 8 November 2013
- Periodic Fever
- MEFV Gene
- Autoinflammatory Syndrome
- Index Family
Autoinflammatory disorders are disorders of the innate immune system. Standard genetic testing provided no correct diagnosis in a female patient from a non-consanguineous family of British descent with a colchicine-responsive autosomal dominant periodic fever syndrome.
We aimed to unravel the genetic cause of the symptoms in this family.
Whole exome sequencing was used to screen for novel sequence variants, which were validated by direct Sanger sequencing. Ex-vivo stimulations with peripheral blood mononuclear cells were done to study the functional consequences of the mutation. mRNA and cytokine levels were measured by q-PCR and ELISA, respectively.
Whole exome sequencing revealed a novel missense sequence variant, not seen in around 6800 controls, mapping to exon 8 of the MEFV gene (c.1730C>A; p.T577N), co-segregating perfectly with disease in this family. Other mutations at the same amino acid (c.1730C>G; p.T577S; c.1729A>T; p.T577S) were found in a family of Turkish descent, with autosomal dominant inheritance of FMF-like phenotype, and a Dutch patient, respectively. Moreover, a mutation (c.1729A>G; p.T577A) was detected in 2 Dutch siblings, suffering from episodes of inflammation of varying severity not resembling FMF. PBMCs from one patient of the index family revealed increased basal IL-1β mRNA levels and cytokine responses after LPS stimulation. Responses normalized under colchicine treatment.
Heterozygous mutations at amino acid position 577 of pyrin can induce an autosomal dominant autoinflammatory syndrome. This suggests that T577, located in front of the C-terminal B30.2/SPRY domain, is crucial for pyrin function.
M. Stoffels: None declared, A. Szperl: None declared, A. Simon Consultant for: Novartis and Swedish Orphan Biovitrum, M. Netea: None declared, T. Plantinga: None declared, M. van Deuren: None declared, S. Kamphuis: None declared, H. Lachmann: None declared, E. Cuppen: None declared, W. Kloosterman: None declared, J. Frenkel Consultant for: Novartis and Swedish Orphan Biovitrum, C. van Diemen: None declared, C. Wijmenga: None declared, M. van Gijn: None declared, J. van der Meer Consultant for: Novartis and Swedish Orphan Biovitrum
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.