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International Immunology, Vol. 14, No. 1, 65-68, January 2002
© 2002 Japanese Society for Immunology

Functional expression of indoleamine 2,3-dioxygenase by murine CD8{alpha}+ dendritic cells

Francesca Fallarino, Carmine Vacca, Ciriana Orabona, Maria L. Belladonna, Roberta Bianchi, Brendan Marshall1, Derin B. Keskin1, Andrew L. Mellor1, Maria C. Fioretti, Ursula Grohmann and Paolo Puccetti

Department of Experimental Medicine, University of Perugia, Via del Giochetto, Perugia 06122, Italy
1 Institute of Molecular Medicine and Genetics, Medical College of Georgia, 1120 15th Street, Augusta, GA 30912, USA

Correspondence to: P. Puccetti

Immunoregulatory antigen-presenting cells (APC) play an important role in maintaining T cell homeostasis and self-tolerance. In particular, recent evidence demonstrates a role for inhibition of T cell proliferation by macrophage tryptophan catabolism involving the activity of the enzyme indoleamine 2,3-dioxygenase (IDO). Dendritic cells (DC) have also been shown to exert immunoregulatory effects mediated by tryptophan catabolism and to cause T cell apoptosis. In the present study, we have comparatively analyzed the expression of IDO activity by murine macrophages and splenic DC. By means of PCR, Western blotting and measurements of enzyme functional activity, we obtained evidence that, different from macrophages, DC constitutively express IDO. Following activation by IFN-{gamma}, the latter cells, in particular the CD8{alpha}+ subset, exhibit high functional activity and, unlike macrophages, mediate apoptosis of Th cells in vitro. Therefore, in the mouse, CD8{alpha}+ DC may be unique APC capable of fully expressing the IDO mechanism functionally.

Keywords: antigen-presenting cells, indoleamine 2,3-dioxygenase, T cell apoptosis, tryptophan metabolism

Transmitting editor: K. Murphy


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