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Epstein-Barr Virus-Infected B Cells Expanding in Germinal Centers of Infectious Mononucleosis Patients Do Not Participate in the Germinal Center Reaction
To assess the impact of the germinal center (GC) reaction on viral spread in Epstein-Barr virus (EBV) infection, we isolated EBV+GC B cells from the tonsils of two infectious mononucleosis patients, sequenced their rearranged V genes, and determined expression of the EBV latency genes EBV nuclear an...
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Published in: | Proceedings of the National Academy of Sciences - PNAS 2003-04, Vol.100 (8), p.4730-4735 |
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description | To assess the impact of the germinal center (GC) reaction on viral spread in Epstein-Barr virus (EBV) infection, we isolated EBV+GC B cells from the tonsils of two infectious mononucleosis patients, sequenced their rearranged V genes, and determined expression of the EBV latency genes EBV nuclear antigen 2 and latent membrane protein 1. Most EBV+GC B cells belonged to clones of cells harboring somatically mutated V gene rearrangements. Ongoing somatic hypermutation, the hallmark of the GC reaction, was seen only in uninfected GC B cell clones, not in EBV+B cell clones. Thus, in infectious mononucleosis, GC and/or memory B cells are directly infected by EBV and expand without somatic hypermutation, whereas the GC passage of EBV-infected naive B cells does not contribute detectably to the generation of infected memory B cells, the main reservoir of EBV during persistence. Most, if not all, EBV-infected cells in GCs exhibited an unusual EBV gene expression pattern in that they were positive for EBV nuclear antigen 2 but negative for latent membrane protein 1. Although the three main types of EBV-associated B cell lymphomas (Burkitt's, Hodgkin's, and posttransplant lymphomas) presumably are derived from GC B cells, EBV+GC B cells resembling these EBV+GC B cell lymphomas in terms of EBV gene expression and somatic hypermutation pattern could not be identified. |
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Most EBV+GC B cells belonged to clones of cells harboring somatically mutated V gene rearrangements. Ongoing somatic hypermutation, the hallmark of the GC reaction, was seen only in uninfected GC B cell clones, not in EBV+B cell clones. Thus, in infectious mononucleosis, GC and/or memory B cells are directly infected by EBV and expand without somatic hypermutation, whereas the GC passage of EBV-infected naive B cells does not contribute detectably to the generation of infected memory B cells, the main reservoir of EBV during persistence. Most, if not all, EBV-infected cells in GCs exhibited an unusual EBV gene expression pattern in that they were positive for EBV nuclear antigen 2 but negative for latent membrane protein 1. Although the three main types of EBV-associated B cell lymphomas (Burkitt's, Hodgkin's, and posttransplant lymphomas) presumably are derived from GC B cells, EBV+GC B cells resembling these EBV+GC B cell lymphomas in terms of EBV gene expression and somatic hypermutation pattern could not be identified.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.2627966100</identifier><identifier>PMID: 12665622</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Adolescent ; Adult ; B lymphocytes ; B-Lymphocytes - immunology ; B-Lymphocytes - pathology ; B-Lymphocytes - virology ; Base Sequence ; Biological Sciences ; Cell lines ; Cells ; DNA, Viral - genetics ; DNA, Viral - isolation & purification ; Epstein Barr virus infections ; Epstein-Barr virus ; Gene Expression ; Genes ; Genes, Viral ; Germinal Center - immunology ; Germinal Center - pathology ; Germinal Center - virology ; Herpesvirus 4, Human - genetics ; Herpesvirus 4, Human - immunology ; Herpesvirus 4, Human - pathogenicity ; Humans ; Immunology ; Infections ; Infectious Mononucleosis - immunology ; Infectious Mononucleosis - pathology ; Infectious Mononucleosis - virology ; Lymphoid tissue ; Lymphoma ; Lymphoma, B-Cell - etiology ; Male ; Molecular Sequence Data ; Palatine tonsils ; Polymerase chain reaction ; T lymphocytes ; Viruses</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2003-04, Vol.100 (8), p.4730-4735</ispartof><rights>Copyright 1993-2003 National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Apr 15, 2003</rights><rights>Copyright © 2003, The National Academy of Sciences 2003</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c522t-144f52afa229bf3076e02aa9acb3ceab38c9845699eff3643d083f4a414fbdfc3</citedby><cites>FETCH-LOGICAL-c522t-144f52afa229bf3076e02aa9acb3ceab38c9845699eff3643d083f4a414fbdfc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/100/8.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/3144010$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/3144010$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792,58237,58470</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12665622$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kurth, Julia</creatorcontrib><creatorcontrib>Hansmann, Martin-Leo</creatorcontrib><creatorcontrib>Rajewsky, Klaus</creatorcontrib><creatorcontrib>Küppers, Ralf</creatorcontrib><title>Epstein-Barr Virus-Infected B Cells Expanding in Germinal Centers of Infectious Mononucleosis Patients Do Not Participate in the Germinal Center Reaction</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>To assess the impact of the germinal center (GC) reaction on viral spread in Epstein-Barr virus (EBV) infection, we isolated EBV+GC B cells from the tonsils of two infectious mononucleosis patients, sequenced their rearranged V genes, and determined expression of the EBV latency genes EBV nuclear antigen 2 and latent membrane protein 1. Most EBV+GC B cells belonged to clones of cells harboring somatically mutated V gene rearrangements. Ongoing somatic hypermutation, the hallmark of the GC reaction, was seen only in uninfected GC B cell clones, not in EBV+B cell clones. Thus, in infectious mononucleosis, GC and/or memory B cells are directly infected by EBV and expand without somatic hypermutation, whereas the GC passage of EBV-infected naive B cells does not contribute detectably to the generation of infected memory B cells, the main reservoir of EBV during persistence. Most, if not all, EBV-infected cells in GCs exhibited an unusual EBV gene expression pattern in that they were positive for EBV nuclear antigen 2 but negative for latent membrane protein 1. Although the three main types of EBV-associated B cell lymphomas (Burkitt's, Hodgkin's, and posttransplant lymphomas) presumably are derived from GC B cells, EBV+GC B cells resembling these EBV+GC B cell lymphomas in terms of EBV gene expression and somatic hypermutation pattern could not be identified.</description><subject>Adolescent</subject><subject>Adult</subject><subject>B lymphocytes</subject><subject>B-Lymphocytes - immunology</subject><subject>B-Lymphocytes - pathology</subject><subject>B-Lymphocytes - virology</subject><subject>Base Sequence</subject><subject>Biological Sciences</subject><subject>Cell lines</subject><subject>Cells</subject><subject>DNA, Viral - genetics</subject><subject>DNA, Viral - isolation & purification</subject><subject>Epstein Barr virus infections</subject><subject>Epstein-Barr virus</subject><subject>Gene Expression</subject><subject>Genes</subject><subject>Genes, Viral</subject><subject>Germinal Center - immunology</subject><subject>Germinal Center - pathology</subject><subject>Germinal Center - virology</subject><subject>Herpesvirus 4, Human - genetics</subject><subject>Herpesvirus 4, Human - immunology</subject><subject>Herpesvirus 4, Human - pathogenicity</subject><subject>Humans</subject><subject>Immunology</subject><subject>Infections</subject><subject>Infectious Mononucleosis - immunology</subject><subject>Infectious Mononucleosis - pathology</subject><subject>Infectious Mononucleosis - virology</subject><subject>Lymphoid tissue</subject><subject>Lymphoma</subject><subject>Lymphoma, B-Cell - etiology</subject><subject>Male</subject><subject>Molecular Sequence Data</subject><subject>Palatine tonsils</subject><subject>Polymerase chain reaction</subject><subject>T lymphocytes</subject><subject>Viruses</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNqFkktvEzEUhUcIRENhzQYhiwWspr1-jGe8YEHTUCqVhxCwtRzHbh1N7MH2VOWn8G_xKFFTKiRWlnW_c3R9fKrqOYYjDC09HrxKR4STVnCOAR5UMwwC15wJeFjNAEhbd4ywg-pJSmsAEE0Hj6sDTDhvOCGz6vdiSNk4X5-oGNEPF8dUn3trdDYrdILmpu8TWtwMyq-cv0TOozMTN86rvsx8NjGhYNFW4cKY0Mfggx91b0JyCX1R2RUsodOAPoVc7jE77QaVzeSVr8x9P_TVqMnKP60eWdUn82x3Hlbf3y--zT_UF5_PzufvLmrdEJJrzJhtiLKKELG0FFpugCgllF5SbdSSdlp0rOFCGGspZ3QFHbVMMczscmU1Pazebn2HcbkxK122iKqXQ3QbFX_JoJz8e-LdlbwM1xI3lBNW9K93-hh-jiZluXFJl9yUNyUQ2VIsiGja_4K4a4kANjm-ugeuwxhLREkSwJRy3PICHW8hHUNK0djbjTHIqRty6obcd6MoXt596J7flaEAb3bApNzbgewkaylIO_Z9Njf5jtW_yQK82ALrlEO8JWj5LcBA_wANdtlf</recordid><startdate>20030415</startdate><enddate>20030415</enddate><creator>Kurth, Julia</creator><creator>Hansmann, Martin-Leo</creator><creator>Rajewsky, Klaus</creator><creator>Küppers, Ralf</creator><general>National Academy of Sciences</general><general>National Acad Sciences</general><general>The National Academy of Sciences</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20030415</creationdate><title>Epstein-Barr Virus-Infected B Cells Expanding in Germinal Centers of Infectious Mononucleosis Patients Do Not Participate in the Germinal Center Reaction</title><author>Kurth, Julia ; 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Most EBV+GC B cells belonged to clones of cells harboring somatically mutated V gene rearrangements. Ongoing somatic hypermutation, the hallmark of the GC reaction, was seen only in uninfected GC B cell clones, not in EBV+B cell clones. Thus, in infectious mononucleosis, GC and/or memory B cells are directly infected by EBV and expand without somatic hypermutation, whereas the GC passage of EBV-infected naive B cells does not contribute detectably to the generation of infected memory B cells, the main reservoir of EBV during persistence. Most, if not all, EBV-infected cells in GCs exhibited an unusual EBV gene expression pattern in that they were positive for EBV nuclear antigen 2 but negative for latent membrane protein 1. Although the three main types of EBV-associated B cell lymphomas (Burkitt's, Hodgkin's, and posttransplant lymphomas) presumably are derived from GC B cells, EBV+GC B cells resembling these EBV+GC B cell lymphomas in terms of EBV gene expression and somatic hypermutation pattern could not be identified.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>12665622</pmid><doi>10.1073/pnas.2627966100</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult B lymphocytes B-Lymphocytes - immunology B-Lymphocytes - pathology B-Lymphocytes - virology Base Sequence Biological Sciences Cell lines Cells DNA, Viral - genetics DNA, Viral - isolation & purification Epstein Barr virus infections Epstein-Barr virus Gene Expression Genes Genes, Viral Germinal Center - immunology Germinal Center - pathology Germinal Center - virology Herpesvirus 4, Human - genetics Herpesvirus 4, Human - immunology Herpesvirus 4, Human - pathogenicity Humans Immunology Infections Infectious Mononucleosis - immunology Infectious Mononucleosis - pathology Infectious Mononucleosis - virology Lymphoid tissue Lymphoma Lymphoma, B-Cell - etiology Male Molecular Sequence Data Palatine tonsils Polymerase chain reaction T lymphocytes Viruses |
title | Epstein-Barr Virus-Infected B Cells Expanding in Germinal Centers of Infectious Mononucleosis Patients Do Not Participate in the Germinal Center Reaction |
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