Epstein-Barr Virus-Associated γδ T-Cell Lymphoproliferative Disorder Associated With Hypomorphic IL2RG Mutation
Chronic active Epstein-Barr virus (EBV) infection (CAEBV) is an EBV-associated lymphoproliferative disease characterized by repeated or sustainable infectious mononucleosis (IM)-like symptoms. EBV is usually detected in B cells in patients who have IM or Burkitt's lymphoma and even in patients...
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Frontiers Media S.A.
2019-02-01
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Series: | Frontiers in Pediatrics |
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Online Access: | https://www.frontiersin.org/article/10.3389/fped.2019.00015/full |
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Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Kay Tanita Akihiro Hoshino Ken-Ichi Imadome Takahiro Kamiya Kento Inoue Tsubasa Okano Tzu-wen Yeh Masakatsu Yanagimachi Akira Shiraishi Masataka Ishimura Tilmann Schober Meino Rohlfs Masatoshi Takagi Kohsuke Imai Hidetoshi Takada Shouichi Ohga Christoph Klein Tomohiro Morio Hirokazu Kanegane |
spellingShingle |
Kay Tanita Akihiro Hoshino Ken-Ichi Imadome Takahiro Kamiya Kento Inoue Tsubasa Okano Tzu-wen Yeh Masakatsu Yanagimachi Akira Shiraishi Masataka Ishimura Tilmann Schober Meino Rohlfs Masatoshi Takagi Kohsuke Imai Hidetoshi Takada Shouichi Ohga Christoph Klein Tomohiro Morio Hirokazu Kanegane Epstein-Barr Virus-Associated γδ T-Cell Lymphoproliferative Disorder Associated With Hypomorphic IL2RG Mutation Frontiers in Pediatrics chronic active Epstein-Barr virus infection γδT-cell common γ chain IL2RG JAK/STAT pathway |
author_facet |
Kay Tanita Akihiro Hoshino Ken-Ichi Imadome Takahiro Kamiya Kento Inoue Tsubasa Okano Tzu-wen Yeh Masakatsu Yanagimachi Akira Shiraishi Masataka Ishimura Tilmann Schober Meino Rohlfs Masatoshi Takagi Kohsuke Imai Hidetoshi Takada Shouichi Ohga Christoph Klein Tomohiro Morio Hirokazu Kanegane |
author_sort |
Kay Tanita |
title |
Epstein-Barr Virus-Associated γδ T-Cell Lymphoproliferative Disorder Associated With Hypomorphic IL2RG Mutation |
title_short |
Epstein-Barr Virus-Associated γδ T-Cell Lymphoproliferative Disorder Associated With Hypomorphic IL2RG Mutation |
title_full |
Epstein-Barr Virus-Associated γδ T-Cell Lymphoproliferative Disorder Associated With Hypomorphic IL2RG Mutation |
title_fullStr |
Epstein-Barr Virus-Associated γδ T-Cell Lymphoproliferative Disorder Associated With Hypomorphic IL2RG Mutation |
title_full_unstemmed |
Epstein-Barr Virus-Associated γδ T-Cell Lymphoproliferative Disorder Associated With Hypomorphic IL2RG Mutation |
title_sort |
epstein-barr virus-associated γδ t-cell lymphoproliferative disorder associated with hypomorphic il2rg mutation |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Pediatrics |
issn |
2296-2360 |
publishDate |
2019-02-01 |
description |
Chronic active Epstein-Barr virus (EBV) infection (CAEBV) is an EBV-associated lymphoproliferative disease characterized by repeated or sustainable infectious mononucleosis (IM)-like symptoms. EBV is usually detected in B cells in patients who have IM or Burkitt's lymphoma and even in patients with X-linked lymphoproliferative syndrome, which is confirmed to have vulnerability to EBV infection. In contrast, EBV infects T cells (CD4+ T, CD8+ T, and γδT) or NK cells mono- or oligoclonally in CAEBV patients. It is known that the CAEBV phenotypes differ depending on which cells are infected with EBV. CAEBV is postulated to be associated with a genetic immunological abnormality, although its cause remains undefined. Here we describe a case of EBV-related γδT-cell proliferation with underlying hypomorphic IL2RG mutation. The immunological phenotype consisted of γδT-cell proliferation in the peripheral blood. A presence of EBV-infected B cells and γδT cells mimicked γδT-cell-type CAEBV. Although the patient had normal expression of CD132 (common γ chain), the phosphorylation of STAT was partially defective, indicating impaired activation of the downstream signal of the JAK/STAT pathway. Although the patient was not diagnosed as having CAEBV, this observation shows that CAEBV might be associated with immunological abnormality. |
topic |
chronic active Epstein-Barr virus infection γδT-cell common γ chain IL2RG JAK/STAT pathway |
url |
https://www.frontiersin.org/article/10.3389/fped.2019.00015/full |
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doaj-f9fa48da9746493b9db8dbcd6a8684202020-11-24T23:17:58ZengFrontiers Media S.A.Frontiers in Pediatrics2296-23602019-02-01710.3389/fped.2019.00015426774Epstein-Barr Virus-Associated γδ T-Cell Lymphoproliferative Disorder Associated With Hypomorphic IL2RG MutationKay Tanita0Akihiro Hoshino1Ken-Ichi Imadome2Takahiro Kamiya3Kento Inoue4Tsubasa Okano5Tzu-wen Yeh6Masakatsu Yanagimachi7Akira Shiraishi8Masataka Ishimura9Tilmann Schober10Meino Rohlfs11Masatoshi Takagi12Kohsuke Imai13Hidetoshi Takada14Shouichi Ohga15Christoph Klein16Tomohiro Morio17Hirokazu Kanegane18Department of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, JapanDepartment of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, JapanDepartment of Advanced Medicine for Virus Infections, National Center for Child Health and Development, Tokyo, JapanDepartment of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, JapanDepartment of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, JapanDepartment of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, JapanDepartment of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, JapanDepartment of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, JapanDepartment of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, JapanDepartment of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, JapanDepartment of Pediatrics, Dr. von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians-University Munich, Munich, GermanyDepartment of Pediatrics, Dr. von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians-University Munich, Munich, GermanyDepartment of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, JapanDepartment of Community Pediatrics, Perinatal and Maternal Medicine, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, JapanDepartment of Child Health, Faculty of Medicine, University of Tsukuba, Tsukuba, JapanDepartment of Pediatrics, Graduate School of Medical Sciences, Kyushu University, Fukuoka, JapanDepartment of Pediatrics, Dr. von Hauner Children's Hospital, University Hospital, Ludwig-Maximilians-University Munich, Munich, GermanyDepartment of Pediatrics and Developmental Biology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, JapanDepartment of Child Health and Development, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, JapanChronic active Epstein-Barr virus (EBV) infection (CAEBV) is an EBV-associated lymphoproliferative disease characterized by repeated or sustainable infectious mononucleosis (IM)-like symptoms. EBV is usually detected in B cells in patients who have IM or Burkitt's lymphoma and even in patients with X-linked lymphoproliferative syndrome, which is confirmed to have vulnerability to EBV infection. In contrast, EBV infects T cells (CD4+ T, CD8+ T, and γδT) or NK cells mono- or oligoclonally in CAEBV patients. It is known that the CAEBV phenotypes differ depending on which cells are infected with EBV. CAEBV is postulated to be associated with a genetic immunological abnormality, although its cause remains undefined. Here we describe a case of EBV-related γδT-cell proliferation with underlying hypomorphic IL2RG mutation. The immunological phenotype consisted of γδT-cell proliferation in the peripheral blood. A presence of EBV-infected B cells and γδT cells mimicked γδT-cell-type CAEBV. Although the patient had normal expression of CD132 (common γ chain), the phosphorylation of STAT was partially defective, indicating impaired activation of the downstream signal of the JAK/STAT pathway. Although the patient was not diagnosed as having CAEBV, this observation shows that CAEBV might be associated with immunological abnormality.https://www.frontiersin.org/article/10.3389/fped.2019.00015/fullchronic active Epstein-Barr virus infectionγδT-cellcommon γ chainIL2RGJAK/STAT pathway |