Monocyte-derived dendritic cells from patients with severe forms of chromoblastomycosis induce CD4⁺ T cell activation in vitro

Dendritic cells (DCs) have been described as initiators and modulators of the immune response. Recently we have shown a predominant production of interleukin-10 cytokine, low levels of interferon-γ and inefficient T cell proliferation in patients with severe forms of chromoblastomycosis. Chromoblast...

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Published in:Clinical and experimental immunology Vol. 156; no. 1; pp. 117 - 125
Main Authors: Sousa, M. Glória, Ghosn, E. Eid Bou, Nascimento, R. Ciciro, Bomfim, G. Facchioli, Noal, V, Santiago, K, de Maria Pedrozo e Silva Azevedo, C, Marques, S. Garcia, Gonçalves, A. Guedes, de Castro Lima Santos, D. Wagner, Criado, P. Ricardo, Costa Martins, J. Eduardo, Almeida, S. Rogerio
Format: Journal Article
Language:English
Published: Oxford, UK Oxford, UK : Blackwell Publishing Ltd 01-04-2009
Blackwell Publishing Ltd
Blackwell
Blackwell Science Inc
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Summary:Dendritic cells (DCs) have been described as initiators and modulators of the immune response. Recently we have shown a predominant production of interleukin-10 cytokine, low levels of interferon-γ and inefficient T cell proliferation in patients with severe forms of chromoblastomycosis. Chromoblastomycosis starts with subcutaneous inoculation of Fonsecaea pedrosoi into tissue where DCs are the first line of defence against this microorganism. In the present study, the interaction of F. pedrosoi and DCs obtained from patients with chromoblastomycosis was investigated. Our results showed that DCs from patients exhibited an increased expression of human leucocyte antigen D-related (HLA-DR) and co-stimulatory molecules. In the presence of conidia, the expression of HLA-DR and CD86 was up-regulated by DCs from patients and controls. Finally, we demonstrate the reversal of antigen-specific anergy and a T helper type 1 response mediated by DCs incubated with F. pedrosoi conidea.
Bibliography:http://dx.doi.org/10.1111/j.1365-2249.2008.03870.x
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ISSN:0009-9104
1365-2249
DOI:10.1111/j.1365-2249.2008.03870.x