PD-1 function in apoptosis of T lymphocytes in canine visceral leishmaniasis
Autor: | Vanessa Marim Chiku, Valéria Marçal Felix de Lima, Paulo Sergio Patto dos Santos, Aline Aparecida Correa Leal, Cleber Costa de Martini, Gabriela Lovizutto Venturin, Kathlenn Liezbeth Oliveira Silva, Breno Fernando Martins de Almeida, Flávia de Rezende Eugênio |
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Přispěvatelé: | Universidade Estadual Paulista (Unesp) |
Rok vydání: | 2015 |
Předmět: |
0301 basic medicine
040301 veterinary sciences medicine.drug_class CD3 T-Lymphocytes Immunology Programmed Cell Death 1 Receptor Spleen Apoptosis Biology Monoclonal antibody Peripheral blood mononuclear cell 0403 veterinary science 03 medical and health sciences Antibodies Monoclonal Murine-Derived Immune system Dogs Canine visceral leishmaniasis medicine Immunology and Allergy Animals PD-1 (programmed cell death 1) Tumor Necrosis Factor-alpha Macrophages 04 agricultural and veterinary sciences Hematology biology.organism_classification Antibodies Neutralizing 030104 developmental biology medicine.anatomical_structure biology.protein Leishmaniasis Visceral Tumor necrosis factor alpha Interleukin-4 Leishmania infantum Antibody Leishmania donovani |
Zdroj: | Scopus Repositório Institucional da UNESP Universidade Estadual Paulista (UNESP) instacron:UNESP |
ISSN: | 1878-3279 |
Popis: | Made available in DSpace on 2018-12-11T17:02:06Z (GMT). No. of bitstreams: 0 Previous issue date: 2016-08-01 Dogs infected with Leishmania infantum have a reduced number of T lymphocytes. PD-1 (Programmed cell death 1) a new member of the B7-CD28 family that is expressed by immune cells, and its binding to PD-L1 (CD274) or PD-L2 (CD273) induces the deactivation or apoptosis of T cells. This study aimed to evaluate the expression of PD-1 and its ligands, as well as blocking in the induction of apoptosis in T lymphocytes, TNF-α, IL-4 and nitric oxide production by leucokocytes from PBMC and spleen and the parasite load in dogs with visceral leishmaniasis (VL). Our results showed that the expression of PD1 and its ligands was increased in CD3+ T cells and CD21+ B lymphocytes within the peripheral blood and splenic mononuclear cells of dogs with VL. In peripheral blood monocytes, only PD-1 ligands exhibited increased expression; however, in spleen macrophages, increased expression of both PD-1 and its ligands was observed. Levels of apoptosis in peripheral blood and splenic T lymphocytes were higher in dogs with VL compared to healthy dogs. Blocking monoclonal antibodies to PD-1 and its ligands in the culture of mononuclear cells from the peripheral blood and spleen decreased the amount of CD3+ T lymphocyte apoptosis. The concentration of nitric oxide, TNF-α and IL-4 increased in the culture supernatants of peripheral blood mononuclear cells treated with a blocking monoclonal antibody against PD-1. The TNF-α concentration increased in the culture supernatants of splenic cells following all treatments with antibodies blocking PD-1 and its ligands; however, the amount of IL-4 increased only in the presence of a PD-1 blocking agent. Treatment with a PD-1 blocking monoclonal antibody in the mononuclear peripheral blood of dogs with VL reduced the parasite burden while increased TNF-α. We conclude that in canine visceral leishmaniasis, PD-1 and its ligands are involved in the induction of T lymphocyte apoptosis and in regulating the production of nitric oxide, TNF-α, and IL-4, as well as the parasitic load. Faculty of Veterinary Medicine of Araçatuba Universidade Estadual Paulista “Julio de Mesquita Filho” FMVA/UNESP, Rua Clovis Pestana, 793, CEP Department of Clinical Care Surgery and Animal Reproduction Laboratory of Cellular Immunology Faculty of Veterinary Medicine of Araçatuba Universidade Estadual Paulista “Julio de Mesquita Filho” FMVA/UNESP, Rua Clovis Pestana, 793, CEP Faculty of Veterinary Medicine of Araçatuba Universidade Estadual Paulista “Julio de Mesquita Filho” FMVA/UNESP, Rua Clovis Pestana, 793, CEP Department of Clinical Care Surgery and Animal Reproduction Laboratory of Cellular Immunology Faculty of Veterinary Medicine of Araçatuba Universidade Estadual Paulista “Julio de Mesquita Filho” FMVA/UNESP, Rua Clovis Pestana, 793, CEP |
Databáze: | OpenAIRE |
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