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Cell Immunol ; 363: 104316, 2021 05.
Article in English | MEDLINE | ID: mdl-33713902

ABSTRACT

Clinical and experimental studies have described eosinophil infiltration in Leishmania amazonensis infection sites, positioning eosinophils strategically adjacent to the protozoan-infected macrophages in cutaneous leishmaniasis. Here, by co-culturing mouse eosinophils with L. amazonensis-infected macrophages, we studied the impact of eosinophils on macrophage ability to regulate intracellular L. amazonensis infection. Eosinophils prevented the increase in amastigote numbers within macrophages by a mechanism dependent on a paracrine activity mediated by eosinophil-derived prostaglandin (PG) D2 acting on DP2 receptors. Exogenous PGD2 mimicked eosinophil-mediated effect on managing L. amazonensis intracellular infection by macrophages and therefore may function as a complementary tool for therapeutic intervention in L. amazonensis-driven cutaneous leishmaniasis.


Subject(s)
Eosinophils/immunology , Leishmaniasis/immunology , Macrophages/immunology , Prostaglandin D2/immunology , Animals , Eosinophils/metabolism , Female , Leishmania/immunology , Leishmaniasis/metabolism , Macrophages/metabolism , Mice , Mice, Inbred BALB C , Paracrine Communication/immunology , Prostaglandin D2/metabolism , Receptors, Prostaglandin/metabolism
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