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Somatic mosaicism in adult‐onset TNF receptor‐associated periodic syndrome (TRAPS)
BACKGROUND: Somatic mosaicism is to date an uncommon finding in genetic autoinflammatory syndromes such as Cryopyrin‐associated periodic syndrome, Blau syndrome, and TNF receptor‐associated periodic syndrome (TRAPS). However, somatic mosaicism may be particularly important in adult‐onset or atypical...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687656/ https://www.ncbi.nlm.nih.gov/pubmed/31397119 http://dx.doi.org/10.1002/mgg3.791 |
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author | Kontzias, Apostolos Zarabi, Samaneh K. Calabrese, Cassandra Wang, Yan Judis, LuAnn Yao, QingPing Cheng, Yu‐Wei |
author_facet | Kontzias, Apostolos Zarabi, Samaneh K. Calabrese, Cassandra Wang, Yan Judis, LuAnn Yao, QingPing Cheng, Yu‐Wei |
author_sort | Kontzias, Apostolos |
collection | PubMed |
description | BACKGROUND: Somatic mosaicism is to date an uncommon finding in genetic autoinflammatory syndromes such as Cryopyrin‐associated periodic syndrome, Blau syndrome, and TNF receptor‐associated periodic syndrome (TRAPS). However, somatic mosaicism may be particularly important in adult‐onset or atypical phenotypes of these conditions. Herein, we report a unique adult‐onset TRAPS patient presenting with intermittent daily fever for 3 weeks, rash, peritonitis, and lymphadenopathy, who was found with hematopoietic mosaicism involving different white blood cell populations. METHODS: Patient's lymphocyte genomic DNA was initially analyzed by periodic fever seven‐gene next‐generation sequencing panel. Genomic DNAs extracted from patient's hair roots, buccal swab, and subpopulations of white blood cells were subsequently examined on the identified TNFRSF1A variant using Sanger sequencing. RESULTS: A de novo mosaic missense variant, c.265 T>C(p.Phe89Leu), in the TNFRSF1A gene was found in the patient's buccal swab, B cells, neutrophils, and NK cells but not detected in monocytes, T cells, and hair roots. CONCLUSION: These data provide additional information about somatic mosaicism in autoinflammatory conditions and provide new insights regarding cellular players that are indispensable for the phenotypic expression of TRAPS. |
format | Online Article Text |
id | pubmed-6687656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-66876562019-08-14 Somatic mosaicism in adult‐onset TNF receptor‐associated periodic syndrome (TRAPS) Kontzias, Apostolos Zarabi, Samaneh K. Calabrese, Cassandra Wang, Yan Judis, LuAnn Yao, QingPing Cheng, Yu‐Wei Mol Genet Genomic Med Clinical Reports BACKGROUND: Somatic mosaicism is to date an uncommon finding in genetic autoinflammatory syndromes such as Cryopyrin‐associated periodic syndrome, Blau syndrome, and TNF receptor‐associated periodic syndrome (TRAPS). However, somatic mosaicism may be particularly important in adult‐onset or atypical phenotypes of these conditions. Herein, we report a unique adult‐onset TRAPS patient presenting with intermittent daily fever for 3 weeks, rash, peritonitis, and lymphadenopathy, who was found with hematopoietic mosaicism involving different white blood cell populations. METHODS: Patient's lymphocyte genomic DNA was initially analyzed by periodic fever seven‐gene next‐generation sequencing panel. Genomic DNAs extracted from patient's hair roots, buccal swab, and subpopulations of white blood cells were subsequently examined on the identified TNFRSF1A variant using Sanger sequencing. RESULTS: A de novo mosaic missense variant, c.265 T>C(p.Phe89Leu), in the TNFRSF1A gene was found in the patient's buccal swab, B cells, neutrophils, and NK cells but not detected in monocytes, T cells, and hair roots. CONCLUSION: These data provide additional information about somatic mosaicism in autoinflammatory conditions and provide new insights regarding cellular players that are indispensable for the phenotypic expression of TRAPS. John Wiley and Sons Inc. 2019-07-10 /pmc/articles/PMC6687656/ /pubmed/31397119 http://dx.doi.org/10.1002/mgg3.791 Text en © 2019 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Clinical Reports Kontzias, Apostolos Zarabi, Samaneh K. Calabrese, Cassandra Wang, Yan Judis, LuAnn Yao, QingPing Cheng, Yu‐Wei Somatic mosaicism in adult‐onset TNF receptor‐associated periodic syndrome (TRAPS) |
title | Somatic mosaicism in adult‐onset TNF receptor‐associated periodic syndrome (TRAPS) |
title_full | Somatic mosaicism in adult‐onset TNF receptor‐associated periodic syndrome (TRAPS) |
title_fullStr | Somatic mosaicism in adult‐onset TNF receptor‐associated periodic syndrome (TRAPS) |
title_full_unstemmed | Somatic mosaicism in adult‐onset TNF receptor‐associated periodic syndrome (TRAPS) |
title_short | Somatic mosaicism in adult‐onset TNF receptor‐associated periodic syndrome (TRAPS) |
title_sort | somatic mosaicism in adult‐onset tnf receptor‐associated periodic syndrome (traps) |
topic | Clinical Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687656/ https://www.ncbi.nlm.nih.gov/pubmed/31397119 http://dx.doi.org/10.1002/mgg3.791 |
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