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Inducible cyclooxygenase released prostaglandin mediates immunosuppression in acute phase of experimental Trypanosoma cruzi infection
Authors:Michelin M A  Silva J S  Cunha F Q C
Affiliation:Department of Biological Sciences, Immunology, Federal School of Medicine, Uberaba, MG, Brazil. michelinimuno@dcb.fmtm.br
Abstract:
We investigated the possible role of prostaglandins produced by COX-2 in the immunosuppression observed during Trypanosoma cruzi infection. Con-A-stimulated splenocytes isolated from mice on days 5, 10, and 15 of infection released large amounts of PGE2 and this release was inhibited by the treatment of animals with sodium salicylate or meloxicam. The treatment of the animals with these drugs enhanced the release of IL-2 by splenocytes from T. cruzi-infected animals and significantly reduced the blood parasitemia and delayed the mortality of the infected mice. Furthermore, the release of TNF-alpha, IFN-gamma, IL-4, and IL-10 by Con-A-stimulated splenocytes obtained from infected mice on days 5, 10, and 15 of the infection was significantly inhibited by treatment of the animals with salicylate or meloxicam. In conclusion, the results suggest that the prostaglandins produced mainly by COX-2 mediate the immunosuppression observed in the acute phase of T. cruzi infection.
Keywords:PGE2, prostaglandin E2   Con-A, concanavalin A   IL, interleukin   TNF-α, tumor necrosis factor α   IFN-γ, interferon γ   COX, cyclooxygenase   Th, T helper   T. cruzi, Trypanosoma cruzi   Ig, immunoglobulin   NO, nitric oxide   MHC, major histocompatibility complex   PBS, phosphate-buffered saline   anti-PGE2, anti-prostaglandin E2 antibody   μCi, microcuries   h, hour   °C, degrees celsius   μg/ml, micrograms per milliliter   BSA, bovine serum albumin   ELISA, enzyme linked immunosorbent assay   nm, nanometers   HE, hematoxylin-eosin   mg/kg, milligrams per kilogram   ng/ml, nanograms per milliliter
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