Current research on chronic active Epstein-Barr virus infection in Japan
Epstein–Barr virus (EBV) infection is usually asymptomatic and persists lifelong. Although EBV‐infected B cells have the potential for unlimited proliferation, they are effectively removed by the virus‐specific cytotoxic T cells, and EBV‐associated lymphoproliferative disease develops only in immuno...
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Veröffentlicht in: | Pediatrics international 2014-04, Vol.56 (2), p.159-166 |
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creator | Fujiwara, Shigeyoshi Kimura, Hiroshi Imadome, Ken-ichi Arai, Ayako Kodama, Eiichi Morio, Tomohiro Shimizu, Norio Wakiguchi, Hiroshi |
description | Epstein–Barr virus (EBV) infection is usually asymptomatic and persists lifelong. Although EBV‐infected B cells have the potential for unlimited proliferation, they are effectively removed by the virus‐specific cytotoxic T cells, and EBV‐associated lymphoproliferative disease develops only in immunocompromised hosts. Rarely, however, individuals without apparent immunodeficiency develop chronic EBV infection with persistent infectious mononucleosis‐like symptoms. These patients have high EBV‐DNA load in the peripheral blood and systemic clonal expansion of EBV‐infected T cells or natural killer (NK) cells. Their prognosis is poor with life‐threatening complications including hemophagocytic lymphohistiocytosis, organ failure, and malignant lymphomas. The term “chronic active EBV infection” (CAEBV) is now generally used for this disease. The geographical distribution of CAEBV is markedly uneven and most cases have been reported from Japan and other East Asian countries. Here we summarize the current understanding of CAEBV and describe the recent progress of CAEBV research in Japan. |
doi_str_mv | 10.1111/ped.12314 |
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Although EBV‐infected B cells have the potential for unlimited proliferation, they are effectively removed by the virus‐specific cytotoxic T cells, and EBV‐associated lymphoproliferative disease develops only in immunocompromised hosts. Rarely, however, individuals without apparent immunodeficiency develop chronic EBV infection with persistent infectious mononucleosis‐like symptoms. These patients have high EBV‐DNA load in the peripheral blood and systemic clonal expansion of EBV‐infected T cells or natural killer (NK) cells. Their prognosis is poor with life‐threatening complications including hemophagocytic lymphohistiocytosis, organ failure, and malignant lymphomas. The term “chronic active EBV infection” (CAEBV) is now generally used for this disease. The geographical distribution of CAEBV is markedly uneven and most cases have been reported from Japan and other East Asian countries. Here we summarize the current understanding of CAEBV and describe the recent progress of CAEBV research in Japan.</description><identifier>ISSN: 1328-8067</identifier><identifier>EISSN: 1442-200X</identifier><identifier>DOI: 10.1111/ped.12314</identifier><identifier>PMID: 24528553</identifier><language>eng</language><publisher>Australia: Blackwell Publishing Ltd</publisher><subject>Animals ; Biomedical Research ; Cell growth ; Child ; chronic active EBV infection ; Chronic Disease ; Cytotoxicity ; Disease Models, Animal ; EBV-associated hemophagocytic lymphohistiocytosis ; EBV-associated T/NK-cell lymphoproliferative disease ; Epstein-Barr virus ; Epstein-Barr Virus Infections - diagnosis ; Epstein-Barr Virus Infections - drug therapy ; Epstein-Barr Virus Infections - physiopathology ; flow-cytometric in situ hybridization ; Herpes viruses ; Humans ; hydroa vacciniforme ; hypersensitivity to mosquito bites ; Japan ; Mice ; mouse model ; Pediatrics</subject><ispartof>Pediatrics international, 2014-04, Vol.56 (2), p.159-166</ispartof><rights>2014 Japan Pediatric Society</rights><rights>2014 Japan Pediatric Society.</rights><rights>Copyright © 2014 Japan Pediatric Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fped.12314$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fped.12314$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27926,27927,45576,45577</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24528553$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fujiwara, Shigeyoshi</creatorcontrib><creatorcontrib>Kimura, Hiroshi</creatorcontrib><creatorcontrib>Imadome, Ken-ichi</creatorcontrib><creatorcontrib>Arai, Ayako</creatorcontrib><creatorcontrib>Kodama, Eiichi</creatorcontrib><creatorcontrib>Morio, Tomohiro</creatorcontrib><creatorcontrib>Shimizu, Norio</creatorcontrib><creatorcontrib>Wakiguchi, Hiroshi</creatorcontrib><title>Current research on chronic active Epstein-Barr virus infection in Japan</title><title>Pediatrics international</title><addtitle>Pediatr Int</addtitle><description>Epstein–Barr virus (EBV) infection is usually asymptomatic and persists lifelong. Although EBV‐infected B cells have the potential for unlimited proliferation, they are effectively removed by the virus‐specific cytotoxic T cells, and EBV‐associated lymphoproliferative disease develops only in immunocompromised hosts. Rarely, however, individuals without apparent immunodeficiency develop chronic EBV infection with persistent infectious mononucleosis‐like symptoms. These patients have high EBV‐DNA load in the peripheral blood and systemic clonal expansion of EBV‐infected T cells or natural killer (NK) cells. Their prognosis is poor with life‐threatening complications including hemophagocytic lymphohistiocytosis, organ failure, and malignant lymphomas. The term “chronic active EBV infection” (CAEBV) is now generally used for this disease. The geographical distribution of CAEBV is markedly uneven and most cases have been reported from Japan and other East Asian countries. Here we summarize the current understanding of CAEBV and describe the recent progress of CAEBV research in Japan.</description><subject>Animals</subject><subject>Biomedical Research</subject><subject>Cell growth</subject><subject>Child</subject><subject>chronic active EBV infection</subject><subject>Chronic Disease</subject><subject>Cytotoxicity</subject><subject>Disease Models, Animal</subject><subject>EBV-associated hemophagocytic lymphohistiocytosis</subject><subject>EBV-associated T/NK-cell lymphoproliferative disease</subject><subject>Epstein-Barr virus</subject><subject>Epstein-Barr Virus Infections - diagnosis</subject><subject>Epstein-Barr Virus Infections - drug therapy</subject><subject>Epstein-Barr Virus Infections - physiopathology</subject><subject>flow-cytometric in situ hybridization</subject><subject>Herpes viruses</subject><subject>Humans</subject><subject>hydroa vacciniforme</subject><subject>hypersensitivity to mosquito bites</subject><subject>Japan</subject><subject>Mice</subject><subject>mouse model</subject><subject>Pediatrics</subject><issn>1328-8067</issn><issn>1442-200X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkTlPAzEQhS0E4i74A2glGpoFn2tvCSHcl1A4Oss4s8KQeBc7C-Tf4ySQgoppZqT53kjzHkJbBO-RVPsN9PcIZYQvoFXCOc0pxk-LaWZU5QoXcgWtxfiKMVZS8WW0QrmgSgi2ik47bQjgR1mACCbYl6z2mX0JtXc2M3bkPiDrNnEEzueHJoTsw4U2Zs5XkJaJdT47N43xG2ipMoMImz99Hd0fd3ud0_zy5uSsc3CZOy4FzwkvBQVGJaHcFpIUQpRWlIVkUlZMYbASl2CVMkZVnPWFkFRSY3FR0P5zBWwd7c7uNqF-byGO9NBFC4OB8VC3URPBuKJluvcPlBSSJlYldOcP-lq3wadHJpQoCSaSJmr7h2qfh9DXTXBDE8b6184E7M-ATzeA8XxPsJ7kpFNOepqTvu0eTYekyGcKlzz-mitMeNMTT4R-vD7R4ujuil70HrRk395ukIs</recordid><startdate>201404</startdate><enddate>201404</enddate><creator>Fujiwara, Shigeyoshi</creator><creator>Kimura, Hiroshi</creator><creator>Imadome, Ken-ichi</creator><creator>Arai, Ayako</creator><creator>Kodama, Eiichi</creator><creator>Morio, Tomohiro</creator><creator>Shimizu, Norio</creator><creator>Wakiguchi, Hiroshi</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TK</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201404</creationdate><title>Current research on chronic active Epstein-Barr virus infection in Japan</title><author>Fujiwara, Shigeyoshi ; Kimura, Hiroshi ; Imadome, Ken-ichi ; Arai, Ayako ; Kodama, Eiichi ; Morio, Tomohiro ; Shimizu, Norio ; Wakiguchi, Hiroshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i4754-14952e327124c6716559c5967377f380ec709ec88aa8f43d557272ac0662dbfe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Biomedical Research</topic><topic>Cell growth</topic><topic>Child</topic><topic>chronic active EBV infection</topic><topic>Chronic Disease</topic><topic>Cytotoxicity</topic><topic>Disease Models, Animal</topic><topic>EBV-associated hemophagocytic lymphohistiocytosis</topic><topic>EBV-associated T/NK-cell lymphoproliferative disease</topic><topic>Epstein-Barr virus</topic><topic>Epstein-Barr Virus Infections - diagnosis</topic><topic>Epstein-Barr Virus Infections - drug therapy</topic><topic>Epstein-Barr Virus Infections - physiopathology</topic><topic>flow-cytometric in situ hybridization</topic><topic>Herpes viruses</topic><topic>Humans</topic><topic>hydroa vacciniforme</topic><topic>hypersensitivity to mosquito bites</topic><topic>Japan</topic><topic>Mice</topic><topic>mouse model</topic><topic>Pediatrics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fujiwara, Shigeyoshi</creatorcontrib><creatorcontrib>Kimura, Hiroshi</creatorcontrib><creatorcontrib>Imadome, Ken-ichi</creatorcontrib><creatorcontrib>Arai, Ayako</creatorcontrib><creatorcontrib>Kodama, Eiichi</creatorcontrib><creatorcontrib>Morio, Tomohiro</creatorcontrib><creatorcontrib>Shimizu, Norio</creatorcontrib><creatorcontrib>Wakiguchi, Hiroshi</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Pediatrics international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fujiwara, Shigeyoshi</au><au>Kimura, Hiroshi</au><au>Imadome, Ken-ichi</au><au>Arai, Ayako</au><au>Kodama, Eiichi</au><au>Morio, Tomohiro</au><au>Shimizu, Norio</au><au>Wakiguchi, Hiroshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Current research on chronic active Epstein-Barr virus infection in Japan</atitle><jtitle>Pediatrics international</jtitle><addtitle>Pediatr Int</addtitle><date>2014-04</date><risdate>2014</risdate><volume>56</volume><issue>2</issue><spage>159</spage><epage>166</epage><pages>159-166</pages><issn>1328-8067</issn><eissn>1442-200X</eissn><abstract>Epstein–Barr virus (EBV) infection is usually asymptomatic and persists lifelong. Although EBV‐infected B cells have the potential for unlimited proliferation, they are effectively removed by the virus‐specific cytotoxic T cells, and EBV‐associated lymphoproliferative disease develops only in immunocompromised hosts. Rarely, however, individuals without apparent immunodeficiency develop chronic EBV infection with persistent infectious mononucleosis‐like symptoms. These patients have high EBV‐DNA load in the peripheral blood and systemic clonal expansion of EBV‐infected T cells or natural killer (NK) cells. Their prognosis is poor with life‐threatening complications including hemophagocytic lymphohistiocytosis, organ failure, and malignant lymphomas. The term “chronic active EBV infection” (CAEBV) is now generally used for this disease. The geographical distribution of CAEBV is markedly uneven and most cases have been reported from Japan and other East Asian countries. Here we summarize the current understanding of CAEBV and describe the recent progress of CAEBV research in Japan.</abstract><cop>Australia</cop><pub>Blackwell Publishing Ltd</pub><pmid>24528553</pmid><doi>10.1111/ped.12314</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Biomedical Research Cell growth Child chronic active EBV infection Chronic Disease Cytotoxicity Disease Models, Animal EBV-associated hemophagocytic lymphohistiocytosis EBV-associated T/NK-cell lymphoproliferative disease Epstein-Barr virus Epstein-Barr Virus Infections - diagnosis Epstein-Barr Virus Infections - drug therapy Epstein-Barr Virus Infections - physiopathology flow-cytometric in situ hybridization Herpes viruses Humans hydroa vacciniforme hypersensitivity to mosquito bites Japan Mice mouse model Pediatrics |
title | Current research on chronic active Epstein-Barr virus infection in Japan |
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