Englander Institute for Precision Medicine

3-hydroxy-L-kynurenamine is an immunomodulatory biogenic amine.

Title3-hydroxy-L-kynurenamine is an immunomodulatory biogenic amine.
Publication TypeJournal Article
Year of Publication2021
AuthorsClement CC, D'Alessandro A, Thangaswamy S, Chalmers S, Furtado R, Spada S, Mondanelli G, Ianni F, Gehrke S, Gargaro M, Manni G, Cara LCarlota Lo, Runge P, Tsai WLi, Karaman S, Arasa J, Fernandez-Rodriguez R, Beck A, Macchiarulo A, Gadina M, Halin C, Fallarino F, Skobe M, Veldhoen M, Moretti S, Formenti S, Demaria S, Soni RK, Galarini R, Sardella R, Lauvau G, Putterman C, Alitalo K, Grohmann U, Santambrogio L
JournalNat Commun
Volume12
Issue1
Pagination4447
Date Published2021 Jul 21
ISSN2041-1723
KeywordsAnimals, Biogenic Amines, Cell Line, Tumor, Dendritic Cells, Disease Models, Animal, Endothelial Cells, Humans, Immunomodulation, Indoleamine-Pyrrole 2,3,-Dioxygenase, Inflammation, Interferon-gamma, Kynurenine, Mice, Nephritis, NF-kappa B, Psoriasis, Tryptophan
Abstract

Tryptophan catabolism is a major metabolic pathway utilized by several professional and non-professional antigen presenting cells to maintain immunological tolerance. Here we report that 3-hydroxy-L-kynurenamine (3-HKA) is a biogenic amine produced via an alternative pathway of tryptophan metabolism. In vitro, 3-HKA has an anti-inflammatory profile by inhibiting the IFN-γ mediated STAT1/NF-κΒ pathway in both mouse and human dendritic cells (DCs) with a consequent decrease in the release of pro-inflammatory chemokines and cytokines, most notably TNF, IL-6, and IL12p70. 3-HKA has protective effects in an experimental mouse model of psoriasis by decreasing skin thickness, erythema, scaling and fissuring, reducing TNF, IL-1β, IFN-γ, and IL-17 production, and inhibiting generation of effector CD8 T cells. Similarly, in a mouse model of nephrotoxic nephritis, besides reducing inflammatory cytokines, 3-HKA improves proteinuria and serum urea nitrogen, overall ameliorating immune-mediated glomerulonephritis and renal dysfunction. Overall, we propose that this biogenic amine is a crucial component of tryptophan-mediated immune tolerance.

DOI10.1038/s41467-021-24785-3
Alternate JournalNat Commun
PubMed ID34290243
PubMed Central IDPMC8295276
Grant ListZIC AR041181 / ImNIH / Intramural NIH HHS / United States
T32 DK007110 / DK / NIDDK NIH HHS / United States
R01 AI103338 / AI / NIAID NIH HHS / United States
R01 AI137198 / AI / NIAID NIH HHS / United States
P30 CA013330 / CA / NCI NIH HHS / United States
R21 AI138552 / AI / NIAID NIH HHS / United States
K12 GM102779 / GM / NIGMS NIH HHS / United States
R01 AG045223 / AG / NIA NIH HHS / United States

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