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Low levels of mannan-binding lectin or ficolins are not associated with an increased risk of cytomegalovirus disease in HIV-infected patients
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 2832632
Author(s) Egli, A.; Schafer, J.; Osthoff, M.; Thiel, S.; Mikkelsen, C.; Rauch, A.; Hirsch, H. H.; Bucher, H. C.; Young, J.; Jensenius, J. C.; Battegay, M.; Trendelenburg, M.
Author(s) at UniBasel Trendelenburg, Marten
Battegay, Manuel E.
Bucher, Heiner
Hirsch, Hans H.
Egli, Adrian
Year 2013
Title Low levels of mannan-binding lectin or ficolins are not associated with an increased risk of cytomegalovirus disease in HIV-infected patients
Journal PLoS ONE
Volume 8
Number 1
Pages / Article-Number e51983
Keywords Adult; Case-Control Studies; Cohort Studies; Cytomegalovirus/ isolation & purification; Cytomegalovirus Infections/ blood/diagnosis/ etiology; Female; HIV/isolation & purification; HIV Infections/blood/ complications/diagnosis; Humans; Lectins/ blood; Male; Mannose-Binding Lectin/ blood; Middle Aged; Risk Factors
Mesh terms Adult; Case-Control Studies; Cohort Studies; Cytomegalovirus, isolation & purification; Cytomegalovirus Infections, etiology; Female; HIV, isolation & purification; HIV Infections, diagnosis; Humans; Lectins, blood; Male; Mannose-Binding Lectin, blood; Middle Aged; Risk Factors
Abstract BACKGROUND: In HIV-infected patients, prediction of Cytomegalovirus (CMV) disease remains difficult. A protective role of mannan-binding lectin (MBL) and ficolins against CMV disease has been reported after transplantation, but the impact in HIV-infected patients is unclear. METHODS: In a case-control study nested within the Swiss HIV Cohort Study, we investigated associations between plasma levels of MBL/ficolins and CMV disease. We compared HIV-infected patients with CMV disease (cases) to CMV-seropositive patients without CMV disease (controls) matched for CD4 T-cells, sampling time, and use of combination antiretroviral therapy. MBL and M-ficolin, L-ficolin, and H-ficolin were quantified using ELISA. RESULTS: We analysed 105 cases and 105 matched controls. CMV disease was neither associated with MBL (odds ratio [OR] 1.03 per log(10) ng/mL increase (95% CI 0.73-1.45)) nor with ficolins (OR per log(10) ng/mL increase 0.66 (95% CI 0.28-1.52), 2.34 (95% CI 0.44-12.36), and 0.89 (95% CI 0.26-3.03) for M-ficolin, L-ficolin, and H-ficolin, respectively). We found no evidence of a greater association between MBL and CMV disease in patients with low CD4 counts; however in the multivariable analysis, CMV disease was more likely in patients with an increased HIV RNA (OR 1.53 per log(10) copies/mL; 95% CI 1.08-2.16), or a shorter duration of HIV-infection (OR 0.91 per year; 95% CI 0.84-0.98). CONCLUSIONS: CMV disease is not associated with low levels of MBL/ficolins, suggesting a lack of a protective role in HIV-infected patients.
Publisher Public Library of Science
ISSN/ISBN 1932-6203
edoc-URL http://edoc.unibas.ch/dok/A6338043
Full Text on edoc No
Digital Object Identifier DOI 10.1371/journal.pone.0051983
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/23308103
ISI-Number WOS:000313670100005
Document type (ISI) Article
 
   

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