@article{10.1172/jci.insight.137131, author = {Jeffrey M. Collins AND Amnah Siddiqa AND Dean P. Jones AND Ken Liu AND Russell R. Kempker AND Azhar Nizam AND N. Sarita Shah AND Nazir Ismail AND Samuel G. Ouma AND Nestani Tukvadze AND Shuzhao Li AND Cheryl L. Day AND Jyothi Rengarajan AND James C.M. Brust AND Neel R. Gandhi AND Joel D. Ernst AND Henry M. Blumberg AND Thomas R. Ziegler}, journal = {JCI Insight}, publisher = {The American Society for Clinical Investigation}, title = {Tryptophan catabolism reflects disease activity in human tuberculosis}, year = {2020}, month = {5}, volume = {5}, url = {https://insight.jci.org/articles/view/137131}, abstract = {There is limited understanding of the role of host metabolism in the pathophysiology of human tuberculosis (TB). Using high-resolution metabolomics with an unbiased approach to metabolic pathway analysis, we discovered that the tryptophan pathway is highly regulated throughout the spectrum of TB infection and disease. This regulation is characterized by increased catabolism of tryptophan to kynurenine, which was evident not only in active TB disease but also in latent TB infection (LTBI). Further, we found that tryptophan catabolism is reversed with effective treatment of both active TB disease and LTBI in a manner commensurate with bacterial clearance. Persons with active TB and LTBI also exhibited increased expression of indoleamine 2,3-dioxygenase-1 (IDO-1), suggesting IDO-1 mediates observed increases in tryptophan catabolism. Together, these data indicate IDO-1–mediated tryptophan catabolism is highly preserved in the human response to Mycobacterium tuberculosis and could be a target for biomarker development as well as host-directed therapies.}, number = {10}, doi = {10.1172/jci.insight.137131}, url = {https://doi.org/10.1172/jci.insight.137131}, }