Source:http://linkedlifedata.com/resource/pubmed/id/21328386
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
2011-2-17
|
pubmed:abstractText |
The etiology of cytomegalovirus (CMV), human herpesvirus-6 (HHV-6), and Epstein-Barr virus (EBV) reactivation and the potential for complications following cytotoxic chemotherapy in the absence of allogeneic transplantation are not clearly understood. Patients with adult T cell leukemia (ATL) are susceptible to opportunistic infections. In this study, the incidence, kinetics and clinical significance of reactivation of CMV, HHV-6, and EBV in ATL patients were investigated. Viral DNA in a total of 468 plasma samples from 34 patients was quantified using real-time PCR. The probability of CMV, HHV-6, and EBV reactivation by 100 days after the start of chemotherapy was 50.6%, 52.3%, and 21.6%, respectively. Although most CMV reactivations were self-limited, plasma CMV DNA tended to persist or increase if the CMV DNA levels in plasma reached ? 10(4) copies/ml. CMV reactivation was negatively associated with survival, but the P-value for this association was near the borderline of statistical significance (P=0.052). One patient developed fatal interstitial pneumonia concomitant with peak CMV DNA accumulation (1.6 × 10(6) ?copies/ml plasma). Most HHV-6 and EBV reactivations were self-limited, and no disease resulting from HHV-6 or EBV was confirmed. HHV-6 and EBV reactivation were not associated with reduced survival (P=0.35 and 0.11, respectively). These findings demonstrated that subclinical reactivation of CMV, HHV-6, and EBV were common in ATL patients receiving chemotherapy. There were differences in the viral reactivation patterns among the three viruses. A CMV load ? 10(4) copies/ml plasma was indicative of subsequent exacerbation of CMV reactivation and developing serious clinical course.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Apr
|
pubmed:issn |
1096-9071
|
pubmed:author |
pubmed-author:AndoTakeakiT,
pubmed-author:IkewakiJunjiJ,
pubmed-author:KadotaJun-ichiJ,
pubmed-author:KawanoRieR,
pubmed-author:KikuchiHiroshiH,
pubmed-author:KohnoKazuhiroK,
pubmed-author:MiyazakiYasuhikoY,
pubmed-author:OgataMasaoM,
pubmed-author:OhtsukaEiichiE,
pubmed-author:SaburiYoshioY,
pubmed-author:SaikawaTetsunoriT,
pubmed-author:SatouTakakoT,
pubmed-author:YoshikawaTetsushiT
|
pubmed:copyrightInfo |
Copyright © 2011 Wiley-Liss, Inc.
|
pubmed:issnType |
Electronic
|
pubmed:volume |
83
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
702-9
|
pubmed:meshHeading |
pubmed-meshheading:21328386-Adult,
pubmed-meshheading:21328386-Aged,
pubmed-meshheading:21328386-Aged, 80 and over,
pubmed-meshheading:21328386-Antineoplastic Agents,
pubmed-meshheading:21328386-Cytomegalovirus Infections,
pubmed-meshheading:21328386-DNA, Viral,
pubmed-meshheading:21328386-Drug Therapy,
pubmed-meshheading:21328386-Epstein-Barr Virus Infections,
pubmed-meshheading:21328386-Female,
pubmed-meshheading:21328386-Humans,
pubmed-meshheading:21328386-Incidence,
pubmed-meshheading:21328386-Leukemia-Lymphoma, Adult T-Cell,
pubmed-meshheading:21328386-Male,
pubmed-meshheading:21328386-Middle Aged,
pubmed-meshheading:21328386-Polymerase Chain Reaction,
pubmed-meshheading:21328386-Roseolovirus Infections,
pubmed-meshheading:21328386-Virus Activation
|
pubmed:year |
2011
|
pubmed:articleTitle |
High incidence of cytomegalovirus, human herpesvirus-6, and Epstein-Barr virus reactivation in patients receiving cytotoxic chemotherapy for adult T cell leukemia.
|
pubmed:affiliation |
Blood Transfusion Center, Oita University Hospital, Oita, Japan. mogata@med.oita-u.ac.jp
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|