File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1002/(SICI)1096-9071(199711)53:3<295::AID-JMV20>3.0.CO;2-F
- Scopus: eid_2-s2.0-0031429631
- PMID: 9365899
- WOS: WOS:A1997YE75500020
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Human herpesvirus-6 and human herpesvirus-7 infections in bone marrow transplant recipients
Title | Human herpesvirus-6 and human herpesvirus-7 infections in bone marrow transplant recipients |
---|---|
Authors | |
Keywords | Antiviral CMV Cofactors Encephalities Myelosuppression PCR |
Issue Date | 1997 |
Publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/32763 |
Citation | Journal Of Medical Virology, 1997, v. 53 n. 3, p. 295-305 How to Cite? |
Abstract | Human cytomegalovirus (HCMV), human herpesvirus-6 (HHV-6), and human herpesvirus-7 (HHV-7) DNA in peripheral blood leukocytes (PBL) of 61 bone marrow transplant recipients was monitored weekly during the first 12 weeks post-transplantation by a nested polymerase chain reaction (PCR). Thirty- seven (61%), 17 (28%), and 23 (53%) of patients had one or more PBL specimens positive for HCMV, HHV-6 or HHV-7 DNA, respectively. HHV-7 DNA in PBL during the early post-transplant period was associated with a longer time to neutrophil engraftment (mean 28.8 days vs 19.8 days; P = 0.01). In two patients who failed to engraft, HHV-6 DNA and HHV-7 DNA was detected in plasma and PBL, respectively, early in their post-transplant period. Patients with HCMV disease were more likely to have concurrent HHV-7 DNA in PBL prior to onset of disease than were patients with asymptomatic HCMV infection, suggesting that HHV-7 may be a cofactor in the progression from HCMV infection to HCMV disease. In the 17 patients (179 specimens) in whom viral DNA in plasma was studied (in addition to PBL), a positive result was found only in 3. In each, viral DNA in plasma appeared to correlate with clinically significant disease. HHV-7 DNA in plasma was associated with encephalitis in an allograft recipient. |
Persistent Identifier | http://hdl.handle.net/10722/157280 |
ISSN | 2023 Impact Factor: 6.8 2023 SCImago Journal Rankings: 1.560 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chan, PKS | en_HK |
dc.contributor.author | Peiris, JSM | en_HK |
dc.contributor.author | Yuen, KY | en_HK |
dc.contributor.author | Liang, RHS | en_HK |
dc.contributor.author | Lau, YL | en_HK |
dc.contributor.author | Chen, FE | en_HK |
dc.contributor.author | Lo, SKF | en_HK |
dc.contributor.author | Cheung, CY | en_HK |
dc.contributor.author | Chan, TK | en_HK |
dc.contributor.author | Ng, MH | en_HK |
dc.date.accessioned | 2012-08-08T08:48:37Z | - |
dc.date.available | 2012-08-08T08:48:37Z | - |
dc.date.issued | 1997 | en_HK |
dc.identifier.citation | Journal Of Medical Virology, 1997, v. 53 n. 3, p. 295-305 | en_HK |
dc.identifier.issn | 0146-6615 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/157280 | - |
dc.description.abstract | Human cytomegalovirus (HCMV), human herpesvirus-6 (HHV-6), and human herpesvirus-7 (HHV-7) DNA in peripheral blood leukocytes (PBL) of 61 bone marrow transplant recipients was monitored weekly during the first 12 weeks post-transplantation by a nested polymerase chain reaction (PCR). Thirty- seven (61%), 17 (28%), and 23 (53%) of patients had one or more PBL specimens positive for HCMV, HHV-6 or HHV-7 DNA, respectively. HHV-7 DNA in PBL during the early post-transplant period was associated with a longer time to neutrophil engraftment (mean 28.8 days vs 19.8 days; P = 0.01). In two patients who failed to engraft, HHV-6 DNA and HHV-7 DNA was detected in plasma and PBL, respectively, early in their post-transplant period. Patients with HCMV disease were more likely to have concurrent HHV-7 DNA in PBL prior to onset of disease than were patients with asymptomatic HCMV infection, suggesting that HHV-7 may be a cofactor in the progression from HCMV infection to HCMV disease. In the 17 patients (179 specimens) in whom viral DNA in plasma was studied (in addition to PBL), a positive result was found only in 3. In each, viral DNA in plasma appeared to correlate with clinically significant disease. HHV-7 DNA in plasma was associated with encephalitis in an allograft recipient. | en_HK |
dc.language | eng | en_US |
dc.publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/32763 | en_HK |
dc.relation.ispartof | Journal of Medical Virology | en_HK |
dc.subject | Antiviral | en_HK |
dc.subject | CMV | en_HK |
dc.subject | Cofactors | en_HK |
dc.subject | Encephalities | en_HK |
dc.subject | Myelosuppression | en_HK |
dc.subject | PCR | en_HK |
dc.subject.mesh | Acyclovir - Therapeutic Use | en_US |
dc.subject.mesh | Adolescent | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Antiviral Agents - Therapeutic Use | en_US |
dc.subject.mesh | Bone Marrow Transplantation - Adverse Effects | en_US |
dc.subject.mesh | Child | en_US |
dc.subject.mesh | Child, Preschool | en_US |
dc.subject.mesh | Cytomegalovirus - Drug Effects - Genetics - Isolation & Purification | en_US |
dc.subject.mesh | Dna, Viral - Blood - Drug Effects | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Graft Vs Host Disease | en_US |
dc.subject.mesh | Herpesviridae Infections - Blood - Drug Therapy - Etiology | en_US |
dc.subject.mesh | Herpesvirus 6, Human - Drug Effects - Genetics - Isolation & Purification | en_US |
dc.subject.mesh | Herpesvirus 7, Human - Drug Effects - Genetics - Isolation & Purification | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Leukocytes, Mononuclear - Virology | en_US |
dc.subject.mesh | Longitudinal Studies | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Polymerase Chain Reaction | en_US |
dc.title | Human herpesvirus-6 and human herpesvirus-7 infections in bone marrow transplant recipients | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Peiris, JSM: malik@hkucc.hku.hk | en_HK |
dc.identifier.email | Yuen, KY: kyyuen@hkucc.hku.hk | en_HK |
dc.identifier.email | Liang, RHS: rliang@hku.hk | en_HK |
dc.identifier.email | Lau, YL: lauylung@hku.hk | en_HK |
dc.identifier.email | Cheung, CY: chungey@hkucc.hku.hk | en_HK |
dc.identifier.authority | Peiris, JSM=rp00410 | en_HK |
dc.identifier.authority | Yuen, KY=rp00366 | en_HK |
dc.identifier.authority | Liang, RHS=rp00345 | en_HK |
dc.identifier.authority | Lau, YL=rp00361 | en_HK |
dc.identifier.authority | Cheung, CY=rp00404 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1002/(SICI)1096-9071(199711)53:3<295::AID-JMV20>3.0.CO;2-F | en_HK |
dc.identifier.pmid | 9365899 | - |
dc.identifier.scopus | eid_2-s2.0-0031429631 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0031429631&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 53 | en_HK |
dc.identifier.issue | 3 | en_HK |
dc.identifier.spage | 295 | en_HK |
dc.identifier.epage | 305 | en_HK |
dc.identifier.isi | WOS:A1997YE75500020 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Chan, PKS=7403497792 | en_HK |
dc.identifier.scopusauthorid | Peiris, JSM=7005486823 | en_HK |
dc.identifier.scopusauthorid | Yuen, KY=36078079100 | en_HK |
dc.identifier.scopusauthorid | Liang, RHS=26643224900 | en_HK |
dc.identifier.scopusauthorid | Lau, YL=7201403380 | en_HK |
dc.identifier.scopusauthorid | Chen, FE=17934080100 | en_HK |
dc.identifier.scopusauthorid | Lo, SKF=7401542391 | en_HK |
dc.identifier.scopusauthorid | Cheung, CY=7202061836 | en_HK |
dc.identifier.scopusauthorid | Chan, TK=37076590700 | en_HK |
dc.identifier.scopusauthorid | Ng, MH=7202076421 | en_HK |
dc.identifier.issnl | 0146-6615 | - |