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

Author:

Sousa M Glória1,Ghosn E Eid Bou1,Nascimento R Ciciro1,Bomfim G Facchioli1,Noal V1,Santiago K1,De Maria Pedrozo e Silva Azevedo C2,Marques S Garcia2,Gonçalves A Guedes2,De Castro Lima Santos D Wagner2,Criado P Ricardo3,Costa Martins J Eduardo3,Almeida S Rogerio1

Affiliation:

1. Departamento de Análises Clínicas e Toxicológicas, Faculdade de Ciências Farmacêuticas

2. Departamento de Dermatologia, Faculdade de Medicina- Universidade de São Paulo, SP

3. Departamento de Patologia, Universidade Federal do Maranhão, São Paulo, Brazil

Abstract

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.

Publisher

Oxford University Press (OUP)

Subject

Immunology,Immunology and Allergy

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