43 kDa Glycoprotein (gp43) fromParacoccidioides brasiliensisInduced IL-17A and PGE2 Production by Human Polymorphonuclear Neutrophils: Involvement of TLR2 and TLR4

Author:

Gardizani Taiane Priscila12,Della Coletta Amanda Manoel1,Romagnoli Graziela Gorete3,Puccia Rosana4,Serezani Ana Paula Moreira5,de Campos Soares Ângela Maria Victoriano3,Dias-Melicio Luciane Alarcão16ORCID

Affiliation:

1. Laboratory of Immunopathology and Infectious Agents (LIAI), Experimental Research Unit (UNIPEX), Medical School of Botucatu (FMB), São Paulo State University (UNESP), Av. Professor Montenegro, s/n, Distrito de Rubião Júnior, 18618-687 Botucatu, São Paulo, Brazil

2. Department of Medicine, University Center of Adamantina, Av. Francisco Bellusci, 1000, Distrito Industrial Otavio Gacazzi, 17800-000 Adamantina, São Paulo, Brazil

3. Department of Microbiology and Immunology, Institute of Biosciences (IB), São Paulo State University (UNESP), Av. Professor Montenegro, s/n, Distrito de Rubião Júnior, 18618-687 Botucatu, São Paulo, Brazil

4. Departamento de Microbiologia, Imunologia e Parasitologia, Escola Paulista de Medicina-Universidade Federal de São Paulo, Rua Botucatu, 862, 04023062 São Paulo, São Paulo, Brazil

5. Division of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA

6. Department of Pathology, Medical School of Botucatu (FMB), São Paulo State University (UNESP), Av. Professor Montenegro, s/n, Distrito de Rubião Júnior, 18618-687 Botucatu, São Paulo, Brazil

Abstract

The glycoprotein gp43 is the major antigenic/diagnostic component ofParacoccidioides brasiliensis, one of the etiologic agents of paracoccidioidomycosis (PCM). Gp43 has protective roles in mice, but due to adhesive properties, this glycoprotein has also been associated with immune evasion mechanisms. The present study evaluated gp43 interaction in vitro with Toll-like receptors 2 and 4 (TLR2 and TLR4) present in polymorphonuclear neutrophils (PMNs) from healthy human individuals and the consequent modulation of the immune response through the expression and release of cytokines and eicosanoids. PMNs were incubated in the absence or presence of monoclonal antibodies anti-TLR2 and anti-TLR4 (individually or in combination) before gp43 stimulation. Then, PMNs were analyzed for the expression of both surface receptors and the detection of intracytoplasmic IL-17A and IL-4 using flow cytometry, while the production of PGE2, LTB4, IL-6, IL-10, IL-12, IFN-γ, and TNF-αwas evaluated in the supernatants by enzyme-linked immunosorbent assay (ELISA). Our results showed that gp43 increased TLR2 and TLR4 expression by PMNs and induced PGE2 and IL-17A via TLR4 and TLR2, respectively. Thus, our data suggest that gp43 fromP. brasiliensismight modulate host susceptibility to the fungal infection by affecting PGE2 and IL-17A production.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Publisher

Hindawi Limited

Subject

Immunology,General Medicine,Immunology and Allergy

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