| Literature DB >> 23768493 |
Poornima Parameswaran1, Yi Liu, Krishna M Roskin, Katherine K L Jackson, Vaishali P Dixit, Ji-Yeun Lee, Karen L Artiles, Simona Zompi, Maria José Vargas, Birgitte B Simen, Bozena Hanczaruk, Kim R McGowan, Muhammad A Tariq, Nader Pourmand, Daphne Koller, Angel Balmaseda, Scott D Boyd, Eva Harris, Andrew Z Fire.
Abstract
Dengue is the most prevalent mosquito-borne viral disease in humans, and the lack of early prognostics, vaccines, and therapeutics contributes to immense disease burden. To identify patterns that could be used for sequence-based monitoring of the antibody response to dengue, we examined antibody heavy-chain gene rearrangements in longitudinal peripheral blood samples from 60 dengue patients. Comparing signatures between acute dengue, postrecovery, and healthy samples, we found increased expansion of B cell clones in acute dengue patients, with higher overall clonality in secondary infection. Additionally, we observed consistent antibody sequence features in acute dengue in the highly variable major antigen-binding determinant, complementarity-determining region 3 (CDR3), with specific CDR3 sequences highly enriched in acute samples compared to postrecovery, healthy, or non-dengue samples. Dengue thus provides a striking example of a human viral infection where convergent immune signatures can be identified in multiple individuals. Such signatures could facilitate surveillance of immunological memory in communities.Entities:
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Year: 2013 PMID: 23768493 PMCID: PMC4136508 DOI: 10.1016/j.chom.2013.05.008
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023