Title
Reduced risk of disease during postsecondary dengue virus infections
Date Issued
15 September 2013
Access level
open access
Resource Type
journal article
Author(s)
Olkowski S.
Forshey B.
Morrison A.
Halsey E.
Kochel T.
Scott T.
Stoddard S.
Naval Medical Research Unit Six
Naval Medical Research Unit Six
Abstract
Background. Antibodies induced by infection with any 1 of 4 dengue virus (DENV) serotypes (DENV-1-4) may influence the clinical outcome of subsequent heterologous infections. To quantify potential cross-protective effects, we estimated disease risk as a function of DENV infection, using data from longitudinal studies performed from September 2006 through February 2011 in Iquitos, Peru, during periods of DENV-3 and DENV-4 transmission.Methods. DENV infections before and during the study period were determined by analysis of serial serum samples with virus neutralization tests. Third and fourth infections were classified as postsecondary infections. Dengue fever cases were detected by door-to-door surveillance for acute febrile illness.Results. Among susceptible participants, 39% (420/1077) and 53% (1595/2997) seroconverted to DENV-3 and DENV-4, respectively. Disease was detected in 7% of DENV-3 infections and 10% of DENV-4 infections. Disease during postsecondary infections was reduced by 93% for DENV-3 and 64% for DENV-4, compared with primary and secondary infections. Despite lower disease rates, postsecondary infections constituted a significant proportion of apparent infections (14% [for DENV-3 infections], 45% [for DENV-4 infections]).Conclusions. Preexisting heterotypic antibodies markedly reduced but did not eliminate the risk of disease in this study population. These results improve understanding of how preinfection history can be associated with dengue outcomes and DENV transmission dynamics. © 2013 The Author.
Start page
1026
End page
1033
Volume
208
Issue
6
Language
English
OCDE Knowledge area
EpidemiologÃa
VirologÃa
Subjects
Scopus EID
2-s2.0-84883216648
PubMed ID
Source
Journal of Infectious Diseases
ISSN of the container
00221899
Sponsor(s)
Financial support. This work was supported by the National Institutes of Health (grant R01 AI06934) and the US Military Infectious Disease Research Program (grants S0147_07_LI, S0216_09_LI, and S0263_10_LI); the Research and Policy in Infectious Disease Dynamics program of the Science and Technology Directorate, Department of Homeland Security (to T. W. S.); and the Fogarty International Center, National Institutes of Health (to T. W. S.). Potential conflicts of interest. All authors: No reported conflicts.
Sources of information:
Directorio de Producción CientÃfica
Scopus