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dc.contributor.authorBreijo Dotta, Martín Andrés-
dc.contributor.authorEsteves, Eliane-
dc.contributor.authorBizzarro, Bruna-
dc.contributor.authorLara, Priscila G.-
dc.contributor.authorAssis, Josiane B.-
dc.contributor.authorRocha, Sergio-
dc.contributor.authorPastro, Lucía-
dc.contributor.authorFernández, Cecilia-
dc.contributor.authorMeikle, Ana-
dc.contributor.authorSá-Nunes, Anderson-
dc.date.accessioned2025-07-15T12:21:33Z-
dc.date.available2025-07-15T12:21:33Z-
dc.date.issued2018-
dc.identifier.citationBreijo Dotta, M, Esteves, E, Bizzarro, B, Lara, P, Assis, J, Rocha, S, Pastro, L, Fernández, C, Meikle, A y Sá-Nunes, A. Hematobin is a novel immunomodulatory protein from the saliva of the horn fly Haematobia irritans that inhibits the inflammatory response in murine macrophages. Parasites & Vectors. [en línea] 2018, 11(435), 1-11es
dc.identifier.urihttps://hdl.handle.net/20.500.12008/50616-
dc.description.abstractBackground: The horn fly Haematobia irritans is a blood-sucking ectoparasite responsible for substantial economic loss of livestock. Like other hematophagous arthropods species, the successful blood-feeding of H. irritans is highly dependent on the modulation of the host’s hemostasis and immune system. Here, we evaluated the biological activity of hematobin (HTB), a protein recently identified in the H. irritans saliva, on macrophage biology. The goal was to understand the putative interactions between the components of H. irritans saliva and the early host immune responses. Results: Thioglycolate-elicited peritoneal macrophages from BALB/c mice were stimulated by lipopolysaccharide (LPS) plus interferon-γ (IFN-γ) in the presence or absence of recombinant HTB. The presence of the salivary protein in the cultures inhibited nitric oxide production and decreased the inducible nitric oxide synthase (iNOS) expression induced by LPS plus IFN-γ. The tumor necrosis factor-α (TNF-α) and interleukin-12p40 (IL-12p40) levels were also reduced in the macrophages pre-incubated with HTB; these findings correlated to the decreased NF-κB expression. The biological activities described here were not associated with changes in annexin V binding to macrophages suggesting that HTB does not induce cell death. In addition, the activity of HTB seems to be specific to macrophages because no changes were observed in lymphocyte proliferation or cytokine production. Conclusions: We describe here the first bioactive salivary protein of H. irritans. We characterized its ability to modulate macrophage inflammatory response, and the results can help explain how horn flies modulate the host immune system to feed on blood.es
dc.format.extent11 pes
dc.format.mimetypeapplication/pdfes
dc.language.isoenes
dc.relation.ispartofParasites & Vectors, 2018, 11(435), 1-11es
dc.rightsLas obras depositadas en el Repositorio se rigen por la Ordenanza de los Derechos de la Propiedad Intelectual de la Universidad de la República.(Res. Nº 91 de C.D.C. de 8/III/1994 – D.O. 7/IV/1994) y por la Ordenanza del Repositorio Abierto de la Universidad de la República (Res. Nº 16 de C.D.C. de 07/10/2014)es
dc.subject.otherHAEMATOBIA IRRITANSes
dc.subject.otherSALIVAes
dc.subject.otherSANGREes
dc.subject.otherECTOPARASITOSes
dc.subject.otherRESPUESTA INMUNOLÓGICAes
dc.titleHematobin is a novel immunomodulatory protein from the saliva of the horn fly Haematobia irritans that inhibits the inflammatory response in murine macrophageses
dc.typeArtículoes
dc.contributor.filiacionBreijo Dotta Martín Andrés, Universidad de la República (Uruguay). Facultad de Medicina. Unidad de Reactivos y Biomodelos de Experimentación-
dc.contributor.filiacionEsteves Eliane, University of Sao Paulo (Sao Paulo, Brazil) Department of Immunology. Institute of Biomedical Sciences. Laboratory of Experimental Immunology-
dc.contributor.filiacionBizzarro Bruna, University of Sao Paulo (Sao Paulo, Brazil) Department of Immunology. Institute of Biomedical Sciences. Laboratory of Experimental Immunology-
dc.contributor.filiacionLara Priscila G., University of Sao Paulo (Sao Paulo, Brazil) Department of Immunology. Institute of Biomedical Sciences. Laboratory of Experimental Immunology-
dc.contributor.filiacionAssis Josiane B., University of Sao Paulo (Sao Paulo, Brazil) Department of Immunology. Institute of Biomedical Sciences. Laboratory of Experimental Immunology-
dc.contributor.filiacionRocha Sergio, Universidad de la República (Uruguay). Facultad de Medicina. Unidad de Reactivos y Biomodelos de Experimentación-
dc.contributor.filiacionPastro Lucía, Universidad de la República (Uruguay). Facultad de Ciencias. Laboratorio de Interacciones Moleculares-
dc.contributor.filiacionFernández Cecilia, Universidad de la República (Uruguay). Facultad de Química. Cátedra de Inmunología-
dc.contributor.filiacionMeikle Ana, Universidad de la República (Uruguay). Facultad de Veterinaria. Laboratorio de Técnicas Nucleares-
dc.contributor.filiacionSá-Nunes Anderson, University of Sao Paulo (Sao Paulo, Brazil) Department of Immunology. Institute of Biomedical Sciences. Laboratory of Experimental Immunology ; National Council of Scientific and Technological Development (INCT-EM/CNPq) (Rio de Janeiro, RJ, Brazil.). National Institute of Science and Technology in Molecular Entomology-
dc.rights.licenceLicencia Creative Commons Atribución (CC - By 4.0)es
dc.identifier.doihttps://doi.org/10.1186/s13071-018-3017-z-
Aparece en las colecciones: Publicaciones académicas y científicas - Facultad de Veterinaria

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