Luck, SE;
Emery, VC;
Atkinson, C;
Sharland, M;
Griffiths, PD;
(2016)
Compartmentalized dynamics of cytomegalovirus replication in treated congenital infection.
J Clin Virol
, 82
pp. 152-158.
10.1016/j.jcv.2016.07.018.
Preview |
Text
Griffiths_viral load in cCMV resubmission 23 July 2016.pdf Download (441kB) | Preview |
Preview |
Text
Griffiths_Table 1 viral load.pdf Download (178kB) | Preview |
Preview |
Text
Griffiths_Figure 1 CMV viral load.pdf Download (312kB) | Preview |
Preview |
Text
Griffiths_Figure 2 CMV viral load.pdf Download (175kB) | Preview |
Preview |
Text
Griffiths_Figure 3 CMV viral load.pdf Download (295kB) | Preview |
Preview |
Text
Griffiths_Figure 4 - CMV viral load.pdf Download (309kB) | Preview |
Preview |
Text
Griffiths_supplemental data CMV viral load.pdf Download (291kB) | Preview |
Spreadsheet
Griffiths_Data%20of%20viral%20load%20for%20supplemental%20data%20tables.xlsx Download (11kB) |
Abstract
BACKGROUND: Cytomegalovirus (CMV) is the most prevalent congenital infection in developed countries. A significant number of infected infants develop long-term neurodevelopmental and hearing impairment irrespective of whether disease is detectable at birth. Studies of viral load and replication dynamics have informed the treatment of CMV in adult populations but no similar data exist in neonates. OBJECTIVES: To study CMV virus kinetics in different body fluids of babies treated for congenital infection. STUDY DESIGN: CMV virus load was sequentially analyzed in blood, urine and saliva in 17 babies treated for symptomatic congenital CMV infection. RESULTS: Virus was detectable in the urine and saliva of all babies at baseline but in only 15/17 in blood. At the end of 6 weeks of antiviral treatment CMV remained detectable in 9/14 blood samples, 9/12 urine samples and 4/7 salivary swabs. Median half-life (T1/2) of virus decline in blood was 2.4 days (IQR 1.9-3.3) and basic reproductive number (Ro) was 2.3. Although T1/2 values were similar in urine and saliva to those observed in blood, virus dynamics differed both during and after treatment. CONCLUSIONS: T1/2 and Ro in blood in this group of neonates were similar to values derived from studies of immunocompromised adults. The persistent viremia observed in treated neonates cannot therefore be adequately explained by the virus dynamics early in treatment. The different dynamics exhibited in blood and urine suggests that studying changes in distinct body compartments may assist in further understanding long-term manifestations of disease.
Type: | Article |
---|---|
Title: | Compartmentalized dynamics of cytomegalovirus replication in treated congenital infection. |
Location: | Netherlands |
Open access status: | An open access version is available from UCL Discovery |
DOI: | 10.1016/j.jcv.2016.07.018 |
Publisher version: | http://dx.doi.org/10.1016/j.jcv.2016.07.018 |
Language: | English |
Additional information: | © 2016. This manuscript version is published under a Creative Commons Attribution Non-commercial Non-derivative 4.0 International licence (CC BY-NC-ND 4.0). This licence allows you to share, copy, distribute and transmit the work for personal and non-commercial use providing author and publisher attribution is clearly stated. Further details about CC BY licences are available at http://creativecommons.org/licenses/by/4.0. Access may be initially restricted by the publisher. |
Keywords: | Antiviral treatment, Congenital cytomegalovirus, Virus dynamics, Virus half-life |
UCL classification: | UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Div of Infection and Immunity |
URI: | https://discovery.ucl.ac.uk/id/eprint/1508724 |
Archive Staff Only
View Item |