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Eur J Immunol ; 31(2): 333-44, 2001 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-11180096

RESUMO

The ability of up-regulatory [recombinant (r) IFN-gamma, rIFN-beta and rTNF-alpha] and down-regulatory (rIL-4, rIL-10 and rIL-13) cytokines to control the expression of indoleamine 2,3-dioxygenase (INDO) and anti-Toxoplasma activity in the human fibrosarcoma cell line 2C4 was evaluated. Activation of fibroblasts with rIFN-gamma, rIFN-beta and rTNF-alpha resulted in augmentation of INDO expression and activity leading to 40.0, 25.0 and 27.0 % inhibition of tachyzoite growth, respectively. An additive effect was observed when host cells were incubated with rIFN-gamma plus rTNF-alpha. With regard to the down-regulatory cytokines we observed that IL-4 as well as IL-13, but not IL-10, induced significant inhibition of IFN-gamma-induced control of parasite replication, INDO mRNA expression and tryptophan catabolism. Similarly, IL-4 but not IL-10 inhibited the cell surface expression of HLA-DR and CD2 induced by IFN-gamma. Consistent with these findings we were able to detect by reverse transcription-PCR the expression of mRNA for different chains of IL-4 and IL-13 receptors (IL-4Ralpha, IL-13Ralpha1 and IL-13Ralpha2) but not for IL-10 receptor in the 2C4 and other human lung fibroblast cell lines (LL24 and MRC5). Together our results indicate that IL-4 and IL-13, but not IL-10, are implicated in the negative regulation of IFN-gamma-induced anti-Toxoplasma activity in human cells from fibroblast lineage.


Assuntos
Interferon gama/farmacologia , Interleucina-13/farmacologia , Interleucina-4/farmacologia , Toxoplasma/efeitos dos fármacos , Triptofano Oxigenase/biossíntese , Animais , Antígenos CD2/biossíntese , Células Cultivadas , Indução Enzimática/efeitos dos fármacos , Fibroblastos/parasitologia , Regulação Enzimológica da Expressão Gênica/efeitos dos fármacos , Antígenos HLA-DR/biossíntese , Humanos , Subunidade alfa1 de Receptor de Interleucina-13 , RNA Mensageiro/análise , Receptores de Interleucina/genética , Receptores de Interleucina-10 , Receptores de Interleucina-13 , Receptores de Interleucina-4/genética , Proteínas Recombinantes , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Toxoplasma/fisiologia , Triptofano Oxigenase/antagonistas & inibidores , Triptofano Oxigenase/genética
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