PLoS ONE (Jan 2018)

The association between dengue immunoglobulin G titres with previous clinical dengue infection and white cell counts in Cuban children: A population-based study.

  • Ramón Suárez-Medina,
  • Silvia Josefina Venero-Fernández,
  • Lourdes Batista-Gutierrez,
  • Yanelis de Los Angeles Estrada-Rondon,
  • Anadelis Alfonso-Hernandez,
  • Dulcima Casanave-Guarnaluce,
  • Nieves Sardinas-Baez,
  • Ivette Castillo-Aguilar,
  • Jorge Antonio Febles-Del Toro,
  • Andrew W Fogarty,
  • HINASIC (Historia Natural de la Sibilancia en Cuba/Natural History of Wheezing in Cuba) Study Group

DOI
https://doi.org/10.1371/journal.pone.0207391
Journal volume & issue
Vol. 13, no. 11
p. e0207391

Abstract

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BackgroundThe prevalence of dengue infection is increasing globally. There are few prospective population-based surveillance studies of the immunological and inflammatory consequences of exposure to dengue virus in young children.ObjectiveTo study the association between serologically confirmed prior medical diagnosis of dengue infection and blood measures of systemic inflammation with dengue virus immunoglobulin G levels.MethodsA population-based study of healthy three-year old children living in Havana, Cuba.Results865 individuals provided a blood sample. Fourteen (1.6%) had a prior medical diagnosis of dengue infection, and 851 individuals had no prior medical diagnosis. There was no difference in the serum immunoglobulin G titres between these groups (Mann-Whitney test, p = 0.49). Total white cell count, blood neutrophil and eosinophil counts were linearly associated with a dengue immunoglobulin G value above the median value.ConclusionsThere was no difference between the dengue immunoglobulin G titres in young children who had previously had clinically proven dengue infection compared to those who had no diagnosis of prior infection. This may be a consequence of a relatively high prevalence of sub-clinical infection. A higher dengue immunoglobulin G level was positively associated with a range of inflammatory biomarkers, although these data cannot demonstrate a causal association.