Severe graft rejection, increased immunosuppression, and active CMV infection in renal transplantation
Associations between active cytomegalovirus (CMV) infection, graft rejection, rejection therapy, and clinical signs and symptoms have been shown repeatedly. However, the causes and the sequence of events remain an area of debate. Two hundred twenty five patients with cadaveric renal transplant were...
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Veröffentlicht in: | Journal of medical virology 2006-03, Vol.78 (3), p.394-399 |
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description | Associations between active cytomegalovirus (CMV) infection, graft rejection, rejection therapy, and clinical signs and symptoms have been shown repeatedly. However, the causes and the sequence of events remain an area of debate. Two hundred twenty five patients with cadaveric renal transplant were included in the present study. Clinical signs and symptoms, and the development of active CMV infections were recorded during the first 3 months after renal transplantation. CMV monitoring by pp65‐antigenemia was performed followed by preemptive antiviral therapy. Delayed graft function and severe graft rejection followed by anti T‐cell antibody therapy was associated with the development of active CMV infection. In contrast, the induction therapy with anti‐T‐cell antibodies was not associated with more active CMV infections. Post‐transplant morbidity determined by fever, pneumonia, and duration of hospital stay was increased significantly in patients with active CMV infection. However, in times of preemptive antiviral therapy an increased morbidity occurred in association with severe graft rejection and not with active CMV infection alone. In patients with renal transplantation and preemptive antiviral therapy, the morbidity was no more influenced by the CMV serostatus although the prevalence of active CMV infection was obviously different between CMV exposed (D+/R+,D+/R−, D−/R+) and unexposed (D−/R−) patients. Severe graft rejection and increased immunosuppression could stimulate cooperatively active CMV infections whereas immunosuppression alone may not be as effective. Prevention of severe graft rejection may be important to decrease early post‐transplant morbidity and also the development of active CMV infections after renal transplantation. J. Med. Virol. 78:394–399, 2006. © 2006 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/jmv.20552 |
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However, the causes and the sequence of events remain an area of debate. Two hundred twenty five patients with cadaveric renal transplant were included in the present study. Clinical signs and symptoms, and the development of active CMV infections were recorded during the first 3 months after renal transplantation. CMV monitoring by pp65‐antigenemia was performed followed by preemptive antiviral therapy. Delayed graft function and severe graft rejection followed by anti T‐cell antibody therapy was associated with the development of active CMV infection. In contrast, the induction therapy with anti‐T‐cell antibodies was not associated with more active CMV infections. Post‐transplant morbidity determined by fever, pneumonia, and duration of hospital stay was increased significantly in patients with active CMV infection. However, in times of preemptive antiviral therapy an increased morbidity occurred in association with severe graft rejection and not with active CMV infection alone. In patients with renal transplantation and preemptive antiviral therapy, the morbidity was no more influenced by the CMV serostatus although the prevalence of active CMV infection was obviously different between CMV exposed (D+/R+,D+/R−, D−/R+) and unexposed (D−/R−) patients. Severe graft rejection and increased immunosuppression could stimulate cooperatively active CMV infections whereas immunosuppression alone may not be as effective. Prevention of severe graft rejection may be important to decrease early post‐transplant morbidity and also the development of active CMV infections after renal transplantation. J. Med. Virol. 78:394–399, 2006. © 2006 Wiley‐Liss, Inc.</description><identifier>ISSN: 0146-6615</identifier><identifier>EISSN: 1096-9071</identifier><identifier>DOI: 10.1002/jmv.20552</identifier><identifier>PMID: 16419118</identifier><identifier>CODEN: JMVIDB</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Biological and medical sciences ; Cytomegalovirus ; Cytomegalovirus Infections - physiopathology ; Cytomegalovirus Infections - virology ; Female ; Fever ; Fundamental and applied biological sciences. Psychology ; Graft Rejection ; Human viral diseases ; Humans ; Immunosuppression ; Infectious diseases ; kidney transplantation ; Kidney Transplantation - adverse effects ; Length of Stay ; Leukopenia ; Lymphocyte Depletion ; Male ; Medical sciences ; Microbiology ; Middle Aged ; Miscellaneous ; Phosphoproteins - blood ; Pneumonia ; Retrospective Studies ; Thrombocytopenia ; Viral diseases ; Viral Matrix Proteins - blood ; Virology</subject><ispartof>Journal of medical virology, 2006-03, Vol.78 (3), p.394-399</ispartof><rights>Copyright © 2006 Wiley‐Liss, Inc.</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4222-6881a8bda87561cd5413534678cee420578f46ad7bc3077ebb0e8953de3864be3</citedby><cites>FETCH-LOGICAL-c4222-6881a8bda87561cd5413534678cee420578f46ad7bc3077ebb0e8953de3864be3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjmv.20552$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjmv.20552$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17469523$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16419118$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>von Müller, Lutz</creatorcontrib><creatorcontrib>Schliep, Christian</creatorcontrib><creatorcontrib>Storck, Martin</creatorcontrib><creatorcontrib>Hampl, Walter</creatorcontrib><creatorcontrib>Schmid, Thomas</creatorcontrib><creatorcontrib>Abendroth, Dietmar</creatorcontrib><creatorcontrib>Mertens, Thomas</creatorcontrib><title>Severe graft rejection, increased immunosuppression, and active CMV infection in renal transplantation</title><title>Journal of medical virology</title><addtitle>J. Med. Virol</addtitle><description>Associations between active cytomegalovirus (CMV) infection, graft rejection, rejection therapy, and clinical signs and symptoms have been shown repeatedly. However, the causes and the sequence of events remain an area of debate. Two hundred twenty five patients with cadaveric renal transplant were included in the present study. Clinical signs and symptoms, and the development of active CMV infections were recorded during the first 3 months after renal transplantation. CMV monitoring by pp65‐antigenemia was performed followed by preemptive antiviral therapy. Delayed graft function and severe graft rejection followed by anti T‐cell antibody therapy was associated with the development of active CMV infection. In contrast, the induction therapy with anti‐T‐cell antibodies was not associated with more active CMV infections. Post‐transplant morbidity determined by fever, pneumonia, and duration of hospital stay was increased significantly in patients with active CMV infection. However, in times of preemptive antiviral therapy an increased morbidity occurred in association with severe graft rejection and not with active CMV infection alone. In patients with renal transplantation and preemptive antiviral therapy, the morbidity was no more influenced by the CMV serostatus although the prevalence of active CMV infection was obviously different between CMV exposed (D+/R+,D+/R−, D−/R+) and unexposed (D−/R−) patients. Severe graft rejection and increased immunosuppression could stimulate cooperatively active CMV infections whereas immunosuppression alone may not be as effective. Prevention of severe graft rejection may be important to decrease early post‐transplant morbidity and also the development of active CMV infections after renal transplantation. J. Med. Virol. 78:394–399, 2006. © 2006 Wiley‐Liss, Inc.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Cytomegalovirus</subject><subject>Cytomegalovirus Infections - physiopathology</subject><subject>Cytomegalovirus Infections - virology</subject><subject>Female</subject><subject>Fever</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Graft Rejection</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Immunosuppression</subject><subject>Infectious diseases</subject><subject>kidney transplantation</subject><subject>Kidney Transplantation - adverse effects</subject><subject>Length of Stay</subject><subject>Leukopenia</subject><subject>Lymphocyte Depletion</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microbiology</subject><subject>Middle Aged</subject><subject>Miscellaneous</subject><subject>Phosphoproteins - blood</subject><subject>Pneumonia</subject><subject>Retrospective Studies</subject><subject>Thrombocytopenia</subject><subject>Viral diseases</subject><subject>Viral Matrix Proteins - blood</subject><subject>Virology</subject><issn>0146-6615</issn><issn>1096-9071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtP3DAURq2qqAyPRf9AlU2RKjXgt51lNaI8NEBReSwtx7mpMs2rdjKUf48hA6wQK1u65_uufRD6TPA-wZgeLJvVPsVC0A9oRnAm0wwr8hHNMOEylZKITbQVwhJjrDNKP6FNIjnJCNEzVP6GFXhI_nhbDomHJbih6trvSdU6DzZAkVRNM7ZdGPveQwhPQ9sWiY3gCpL52U1kyykWb7GjtXUyeNuGvrbtYB8HO2ijtHWA3fW5ja5_Hl7Nj9PFxdHJ_McidZxSmkqtidV5YbUSkrhCcMIE41JpB8DjF5UuubSFyh3DSkGeY9CZYAUwLXkObBvtTb297_6NEAbTVMFBHR8C3RiMimIUJuJdMO5iIuM0gt8m0PkuBA-l6X3VWH9vCDaP9k20b57sR_bLunTMGyheybXuCHxdAzY4W5dRkqvCK6e4zGJP5A4m7q6q4f7tjeb07OZ5dTolqjDA_5eE9X-NVEwJc3t-ZM4vqbpc_BLmmD0AVMarGw</recordid><startdate>200603</startdate><enddate>200603</enddate><creator>von Müller, Lutz</creator><creator>Schliep, Christian</creator><creator>Storck, Martin</creator><creator>Hampl, Walter</creator><creator>Schmid, Thomas</creator><creator>Abendroth, Dietmar</creator><creator>Mertens, Thomas</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><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>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200603</creationdate><title>Severe graft rejection, increased immunosuppression, and active CMV infection in renal transplantation</title><author>von Müller, Lutz ; Schliep, Christian ; Storck, Martin ; Hampl, Walter ; Schmid, Thomas ; Abendroth, Dietmar ; Mertens, Thomas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4222-6881a8bda87561cd5413534678cee420578f46ad7bc3077ebb0e8953de3864be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Cytomegalovirus</topic><topic>Cytomegalovirus Infections - physiopathology</topic><topic>Cytomegalovirus Infections - virology</topic><topic>Female</topic><topic>Fever</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Graft Rejection</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Immunosuppression</topic><topic>Infectious diseases</topic><topic>kidney transplantation</topic><topic>Kidney Transplantation - adverse effects</topic><topic>Length of Stay</topic><topic>Leukopenia</topic><topic>Lymphocyte Depletion</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Microbiology</topic><topic>Middle Aged</topic><topic>Miscellaneous</topic><topic>Phosphoproteins - blood</topic><topic>Pneumonia</topic><topic>Retrospective Studies</topic><topic>Thrombocytopenia</topic><topic>Viral diseases</topic><topic>Viral Matrix Proteins - blood</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>von Müller, Lutz</creatorcontrib><creatorcontrib>Schliep, Christian</creatorcontrib><creatorcontrib>Storck, Martin</creatorcontrib><creatorcontrib>Hampl, Walter</creatorcontrib><creatorcontrib>Schmid, Thomas</creatorcontrib><creatorcontrib>Abendroth, Dietmar</creatorcontrib><creatorcontrib>Mertens, Thomas</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of medical virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>von Müller, Lutz</au><au>Schliep, Christian</au><au>Storck, Martin</au><au>Hampl, Walter</au><au>Schmid, Thomas</au><au>Abendroth, Dietmar</au><au>Mertens, Thomas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Severe graft rejection, increased immunosuppression, and active CMV infection in renal transplantation</atitle><jtitle>Journal of medical virology</jtitle><addtitle>J. Med. Virol</addtitle><date>2006-03</date><risdate>2006</risdate><volume>78</volume><issue>3</issue><spage>394</spage><epage>399</epage><pages>394-399</pages><issn>0146-6615</issn><eissn>1096-9071</eissn><coden>JMVIDB</coden><abstract>Associations between active cytomegalovirus (CMV) infection, graft rejection, rejection therapy, and clinical signs and symptoms have been shown repeatedly. However, the causes and the sequence of events remain an area of debate. Two hundred twenty five patients with cadaveric renal transplant were included in the present study. Clinical signs and symptoms, and the development of active CMV infections were recorded during the first 3 months after renal transplantation. CMV monitoring by pp65‐antigenemia was performed followed by preemptive antiviral therapy. Delayed graft function and severe graft rejection followed by anti T‐cell antibody therapy was associated with the development of active CMV infection. In contrast, the induction therapy with anti‐T‐cell antibodies was not associated with more active CMV infections. Post‐transplant morbidity determined by fever, pneumonia, and duration of hospital stay was increased significantly in patients with active CMV infection. However, in times of preemptive antiviral therapy an increased morbidity occurred in association with severe graft rejection and not with active CMV infection alone. In patients with renal transplantation and preemptive antiviral therapy, the morbidity was no more influenced by the CMV serostatus although the prevalence of active CMV infection was obviously different between CMV exposed (D+/R+,D+/R−, D−/R+) and unexposed (D−/R−) patients. Severe graft rejection and increased immunosuppression could stimulate cooperatively active CMV infections whereas immunosuppression alone may not be as effective. Prevention of severe graft rejection may be important to decrease early post‐transplant morbidity and also the development of active CMV infections after renal transplantation. J. Med. Virol. 78:394–399, 2006. © 2006 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>16419118</pmid><doi>10.1002/jmv.20552</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Biological and medical sciences Cytomegalovirus Cytomegalovirus Infections - physiopathology Cytomegalovirus Infections - virology Female Fever Fundamental and applied biological sciences. Psychology Graft Rejection Human viral diseases Humans Immunosuppression Infectious diseases kidney transplantation Kidney Transplantation - adverse effects Length of Stay Leukopenia Lymphocyte Depletion Male Medical sciences Microbiology Middle Aged Miscellaneous Phosphoproteins - blood Pneumonia Retrospective Studies Thrombocytopenia Viral diseases Viral Matrix Proteins - blood Virology |
title | Severe graft rejection, increased immunosuppression, and active CMV infection in renal transplantation |
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