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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
Institution: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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