Robust Phenotypic Activation of Eosinophils during Experimental Toxocara canis Infection
Autor: | Ricardo de Oliveira Correia, Jordana Grazziela Coelho-dos-Reis, Fernanda de Freitas Anibal, Débora Meira Neris, Olindo Assis Martins-Filho, Márcio Sobreira Silva Araújo, Elaine Speziali, Joice Margareth de Almeida Rodolpho, Andréa Teixeira-Carvalho, Luciana Camillo |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
lcsh:Immunologic diseases. Allergy Immunology Spleen Proinflammatory cytokine 03 medical and health sciences 0302 clinical medicine Immune system Antigen medicine Immunology and Allergy Cytotoxic T cell eosinophil biology Toxocara canis Eosinophil co-stimulatory molecules biology.organism_classification 030104 developmental biology medicine.anatomical_structure SLMV activation Bone marrow lcsh:RC581-607 030215 immunology |
Zdroj: | Frontiers in Immunology, Vol 9 (2018) |
ISSN: | 1664-3224 |
DOI: | 10.3389/fimmu.2018.00064/full |
Popis: | Eosinophils are multifunctional cells that have cytotoxic proinflammatory activities and stimulate CD4+ T-cells in experimental models of allergy and parasitic infections. Eosinophils, when exposed to antigens, are activated, expressing the CD38/CD69 molecules and exhibited increased expression of major histocompatibility complex (MHC-II), CD80 and CD86, suggesting they play a role upon Toxocara canis antigen stimulation. In the present study, we evaluated the profile of eosinophils using conventional and image flow cytometry upon experimental T. canis infection. T. canis antigens induced a robust activation on this subset, contributing to the immune responses elicited in the experimental model for T. canis-associated visceral larva migrans syndrome. Data analysis demonstrated that, during murine T. canis infection, eosinophils from peripheral blood, spleen, and bone marrow presented upregulated expression of CD69/MHC-II/CD80/CD86. As opposed to splenic and bone marrow eosinophils, circulating eosinophils had increased expression of activation markers upon T. canis infection. The enhanced connectivity between eosinophils and T-cells in T. canis-infected mice in all three compartments (peripheral blood, spleen, and bone marrow) also supports the hypothesis that eosinophils may adopt a role during T. canis infection. Moreover, in vitro T. canis antigen stimulation resulted in activation and upregulation of co-stimulatory-related molecules by bone marrow-derived eosinophils. Our findings are evidence of activation and upregulation of important activation and co-stimulatory-related molecules in eosinophils and suggest a reshape of activation hierarchy toward eosinophils during experimental T. canis infection. |
Databáze: | OpenAIRE |
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