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Neutralization of dengue virus in the presence of Fc receptor-mediated phagocytosis distinguishes serotype-specific from cross-neutralizing antibodies.
- Source :
-
Antiviral research [Antiviral Res] 2012 Dec; Vol. 96 (3), pp. 340-3. Date of Electronic Publication: 2012 Oct 04. - Publication Year :
- 2012
-
Abstract
- Although several vaccine candidates are presently in various phases of clinical trials, the field still lacks an effective tool to determine protective immunity. The presence of cross-neutralizing antibodies limits a serological approach to identify the etiology and distinguish lifelong from short-lived humoral protection. A recent study indicated that cross-reactive but not serotype-specific antibodies require high antibody concentration to co-ligate FcγRIIB and inhibit infection. Here, we tested if these differences could allow us to distinguish serotype-specific from cross-neutralizing antibodies. Using 30 blinded early convalescent serum samples from patients with virologically confirmed dengue, we demonstrate that neutralization in the presence of FcγR-mediated phagocytosis in THP-1 correctly identifies the DENV serotype of the infection in 93.3% of the cases compared to 76.7% with plaque reduction neutralization test. Our findings could provide a new approach for evaluating DENV neutralization and suggest that in addition to blocking specific ligand-receptor interactions for viral entry, antibodies must prevent viral uncoating during FcγR-mediated phagocytosis for complete humoral protection.<br /> (Copyright © 2012 Elsevier B.V. All rights reserved.)
- Subjects :
- Adult
Antibodies, Viral blood
Antibodies, Viral immunology
Cell Line, Tumor
Dengue immunology
Dengue virology
Dengue Virus classification
Host-Pathogen Interactions
Humans
Neutralization Tests methods
Sensitivity and Specificity
Species Specificity
Viral Plaque Assay
Virus Internalization
Antibodies, Neutralizing immunology
Cross Reactions
Dengue Virus immunology
Phagocytosis
Receptors, IgG immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1872-9096
- Volume :
- 96
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Antiviral research
- Publication Type :
- Academic Journal
- Accession number :
- 23041143
- Full Text :
- https://doi.org/10.1016/j.antiviral.2012.09.018