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Type 1 Innate Lymphoid Cell and Natural Killer Cells Are Sources of Interferon-γ and Other Inflammatory Cytokines Associated With Distinct Clinical Presentation in Early Dengue Infection.

Authors :
Quintino-de-Carvalho, Iracema Luisa
Gonçalves-Pereira, Marcela Helena
Ramos, Michele Faria
Milhim, Bruno Henrique Gonçalves de Aguiar
Costa, Último Libânio Da
Santos, Érika Gonçalves
Nogueira, Maurício Lacerda
Santiago, Helton Da Costa
de Aguiar Milhim, Bruno Henrique Gonçalves
Da Costa, Último Libânio
Faria Ramos, Michele
Da Costa Santiago, Helton
Source :
Journal of Infectious Diseases; 1/1/2022, Vol. 225 Issue 1, p84-93, 10p
Publication Year :
2022

Abstract

<bold>Background: </bold>Increased levels of inflammatory cytokines are associated with severe dengue evolution, but the source of such hypercytokinemia is elusive. We investigated the contribution of innate lymphocytes, innate lymphoid cells (ILCs), and natural killer (NK) cells in cytokine production in early dengue infection.<bold>Methods: </bold>Peripheral blood mononuclear cells of individuals with dengue without warning signs (DWS-) and dengue with warning signs and severe dengue (SD) presentation combined (DWS+) were obtained between 2 and 7 days since fever onset and submitted to flow cytometry without specific antigen stimulation to evaluate cytokines in ILC and NK cell subpopulations.<bold>Results: </bold>ILCs and NK cells were found to be important sources of cytokines during dengue. ILCs of the DWS+/SD group displayed higher production of interferon gamma (IFN-γ) and interleukin (IL) 4/IL-13 when compared to DWS- individuals. On the other hand, NK Eomes+ cells of DWS- patients displayed higher IFN-γ production levels compared with the DWS+/SD group. Interestingly, when NK cells were identified by CD56 expression, DWS+/SD displayed higher frequency of IL-17 production compared with the DWS- group.<bold>Conclusions: </bold>These results indicate that ILCs and NK cells are important sources of inflammatory cytokines during acute dengue infection and display distinct profiles associated with different clinical forms. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00221899
Volume :
225
Issue :
1
Database :
Complementary Index
Journal :
Journal of Infectious Diseases
Publication Type :
Academic Journal
Accession number :
154512134
Full Text :
https://doi.org/10.1093/infdis/jiab312