Please use this identifier to cite or link to this item:
https://www.arca.fiocruz.br/handle/icict/50475
Type
ArticleCopyright
Open access
Collections
- INI - Artigos de Periódicos [3645]
- IOC - Artigos de Periódicos [12973]
Metadata
Show full item record
IL1B RS1143634 (+3953) VARIANT ASSOCIATED WITH SEVERE DENGUE IN BRAZILIAN CHILDREN
Author
Affilliation
University of Antioquia. Biology Institute. Research Group on Molecular Genetics. Medellín, Colombia.
Fundação Oswaldo Cruz. Instituto Nacional de Infectologia Evandro Chagas. Laboratório de Pesquisa Clínica em DST/AIDS. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Hanseníase. Rio de Janeiro, RJ, Brasil.
Universidade Federal do Rio de Janeiro. Instituto de Biologia. Departamento de Genética. Laboratório de Virologia Molecular. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Imunologia Viral. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Hanseníase. Rio de Janeiro, RJ, Brasil.
University of Antioquia. Biology Institute. Research Group on Molecular Genetics. Medellín, Colombia.
Fundação Oswaldo Cruz. Instituto Nacional de Infectologia Evandro Chagas. Laboratório de Pesquisa Clínica em DST/AIDS. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Hanseníase. Rio de Janeiro, RJ, Brasil.
Universidade Federal do Rio de Janeiro. Instituto de Biologia. Departamento de Genética. Laboratório de Virologia Molecular. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Imunologia Viral. Rio de Janeiro, RJ, Brasil.
Fundação Oswaldo Cruz. Instituto Oswaldo Cruz. Laboratório de Hanseníase. Rio de Janeiro, RJ, Brasil.
University of Antioquia. Biology Institute. Research Group on Molecular Genetics. Medellín, Colombia.
Abstract
Several variants involved in the expression of proteins related to immunopathological mechanisms have been
associated with dengue, but few specifically related to severe dengue. In addition, children are a group with a high
incidence and mortality rate due to dengue. Several immunopathological processes developed specifically in children
affected with severe dengue partially explain this risk condition. This case-control retrospective study aimed to
examine the association of variants in CD209, NFKBIA, IL12B, and IL1B genes with severe dengue. These genes
encode proteins involved in one of the main pathways of the immune response against dengue virus infection. The
study population included affected children and householding controls from Brazil. Genotyping was performed with
Real-Time TaqMan assays, and the association analysis was performed with conditional logistic regressions. We
found the IL1B rs1143634 genotypes carrying the T allele to be associated with susceptibility to severe dengue in
children. The lower circulating levels of IL-1β associated with carrying the T allele of the IL1B rs1143634 suggest a
role of this cytokine in the impairment of the immune response and plasma leakage, and, consequently, in the
development of severe dengue.
Share