CDllc+ Cells Modulate Pulmonary Immune Responses by Production of Indoleamine 2,3-Dioxygenase
2004
Interactions between
antigen-presenting cellsand T cells can result in T cell activation or suppression. With the use of RNA analysis, high-performance liquid chromatography, mixed leukocyte reactions (MLRs), and animal models, the current study reports that lung interstitial
antigen-presenting cells(iAPCs, CDllc+) suppress T cell responses in vitro and in vivo by production of
indoleamine 2,3-dioxygenase(IDO), an enzyme that catabolizes tryptophan to its byproduct,
kynurenine. IDO mRNA expression was unique to lung iAPCs, as cells similarly isolated from the liver and spleen did not express IDO constitutively, or in response to interferon-γ. Lung iAPCs suppressed proliferation of allogeneic T cells, correlating with increased
kynureninelevels; and blockade of IDO activity with 1-methyl-DL-tryptohan (1-MT) or addition of exogenous tryptophan recovered T cell proliferation in MLRs. In contrast, liver and splenic iAPCs were potent stimulators of T cells in MLRs, and IDO inhibition had no effect on T
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