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Multiplex cytokine profile from dengue patients: MIP-1beta and IFN-gamma as predictive factors for severity

BACKGROUND: Dengue virus pathogenesis is not yet fully understood and the identification of patients at high risk for developing severe disease forms is still a great challenge in dengue patient care. During the present study, we evaluated prospectively the potential of cytokines present in plasma f...

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Autores principales: Bozza, Fernando A, Cruz, Oswaldo G, Zagne, Sonia MO, Azeredo, Elzinandes L, Nogueira, Rita MR, Assis, Edson F, Bozza, Patricia T, Kubelka, Claire F
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2474613/
https://www.ncbi.nlm.nih.gov/pubmed/18578883
http://dx.doi.org/10.1186/1471-2334-8-86
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author Bozza, Fernando A
Cruz, Oswaldo G
Zagne, Sonia MO
Azeredo, Elzinandes L
Nogueira, Rita MR
Assis, Edson F
Bozza, Patricia T
Kubelka, Claire F
author_facet Bozza, Fernando A
Cruz, Oswaldo G
Zagne, Sonia MO
Azeredo, Elzinandes L
Nogueira, Rita MR
Assis, Edson F
Bozza, Patricia T
Kubelka, Claire F
author_sort Bozza, Fernando A
collection PubMed
description BACKGROUND: Dengue virus pathogenesis is not yet fully understood and the identification of patients at high risk for developing severe disease forms is still a great challenge in dengue patient care. During the present study, we evaluated prospectively the potential of cytokines present in plasma from patients with dengue in stratifying disease severity. METHODS: Seventeen-cytokine multiplex fluorescent microbead immunoassay was used for the simultaneous detection in 59 dengue patients. GLM models using bimodal or Gaussian family were determined in order to associate cytokines with clinical manifestations and laboratory diagnosis. RESULTS: IL-1β, IFN-γ, IL-4, IL-6, IL-13, IL-7 and GM-CSF were significantly increased in patients with severe clinical manifestations (severe dengue) when compared to mild disease forms (mild dengue). In contrast, increased MIP-1β levels were observed in patients with mild dengue. MIP-1β was also associated with CD56+NK cell circulating rates. IL-1β, IL-8, TNF-α and MCP-1 were associated with marked thrombocytopenia. Increased MCP-1 and GM-CSF levels correlated with hypotension. Moreover, MIP-1β and IFN-γ were independently associated with both dengue severity and disease outcome. CONCLUSION: Our data demonstrated that the use of a multiple cytokine assay platform was suitable for identifying distinct cytokine profiles associated with the dengue clinical manifestations and severity. MIP-β is indicated for the first time as a good prognostic marker in contrast to IFN-γ that was associated with disease severity.
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spelling pubmed-24746132008-07-17 Multiplex cytokine profile from dengue patients: MIP-1beta and IFN-gamma as predictive factors for severity Bozza, Fernando A Cruz, Oswaldo G Zagne, Sonia MO Azeredo, Elzinandes L Nogueira, Rita MR Assis, Edson F Bozza, Patricia T Kubelka, Claire F BMC Infect Dis Research Article BACKGROUND: Dengue virus pathogenesis is not yet fully understood and the identification of patients at high risk for developing severe disease forms is still a great challenge in dengue patient care. During the present study, we evaluated prospectively the potential of cytokines present in plasma from patients with dengue in stratifying disease severity. METHODS: Seventeen-cytokine multiplex fluorescent microbead immunoassay was used for the simultaneous detection in 59 dengue patients. GLM models using bimodal or Gaussian family were determined in order to associate cytokines with clinical manifestations and laboratory diagnosis. RESULTS: IL-1β, IFN-γ, IL-4, IL-6, IL-13, IL-7 and GM-CSF were significantly increased in patients with severe clinical manifestations (severe dengue) when compared to mild disease forms (mild dengue). In contrast, increased MIP-1β levels were observed in patients with mild dengue. MIP-1β was also associated with CD56+NK cell circulating rates. IL-1β, IL-8, TNF-α and MCP-1 were associated with marked thrombocytopenia. Increased MCP-1 and GM-CSF levels correlated with hypotension. Moreover, MIP-1β and IFN-γ were independently associated with both dengue severity and disease outcome. CONCLUSION: Our data demonstrated that the use of a multiple cytokine assay platform was suitable for identifying distinct cytokine profiles associated with the dengue clinical manifestations and severity. MIP-β is indicated for the first time as a good prognostic marker in contrast to IFN-γ that was associated with disease severity. BioMed Central 2008-06-25 /pmc/articles/PMC2474613/ /pubmed/18578883 http://dx.doi.org/10.1186/1471-2334-8-86 Text en Copyright © 2008 Bozza et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bozza, Fernando A
Cruz, Oswaldo G
Zagne, Sonia MO
Azeredo, Elzinandes L
Nogueira, Rita MR
Assis, Edson F
Bozza, Patricia T
Kubelka, Claire F
Multiplex cytokine profile from dengue patients: MIP-1beta and IFN-gamma as predictive factors for severity
title Multiplex cytokine profile from dengue patients: MIP-1beta and IFN-gamma as predictive factors for severity
title_full Multiplex cytokine profile from dengue patients: MIP-1beta and IFN-gamma as predictive factors for severity
title_fullStr Multiplex cytokine profile from dengue patients: MIP-1beta and IFN-gamma as predictive factors for severity
title_full_unstemmed Multiplex cytokine profile from dengue patients: MIP-1beta and IFN-gamma as predictive factors for severity
title_short Multiplex cytokine profile from dengue patients: MIP-1beta and IFN-gamma as predictive factors for severity
title_sort multiplex cytokine profile from dengue patients: mip-1beta and ifn-gamma as predictive factors for severity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2474613/
https://www.ncbi.nlm.nih.gov/pubmed/18578883
http://dx.doi.org/10.1186/1471-2334-8-86
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