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J Virol. 2016 Aug 12;90(17):7967-79. doi: 10.1128/JVI.00994-16. Print 2016 Sep 1.

Kynurenine Reduces Memory CD4 T-Cell Survival by Interfering with Interleukin-2 Signaling Early during HIV-1 Infection.

Author information

1
Institut National de la Recherche Scientifique (INRS)-Institut Armand-Frappier, Laval, Québec, Canada.
2
Chronic Viral Illness Service and Division of Hematology, McGill University Health Centre, Montréal, Québec, Canada.
3
Centre de Recherche de l'Université de Montréal, Montréal, Québec, Canada.
4
Center for AIDS Research, Proteomics and Systems Biology, Case Western Reserve University, Cleveland, Ohio, USA.
5
Institut National de la Recherche Scientifique (INRS)-Institut Armand-Frappier, Laval, Québec, Canada julien.vangrevenynghe@iaf.inrs.ca.

Abstract

Early HIV-1 infection is characterized by enhanced tryptophan catabolism, which contributes to immune suppression and disease progression. However, the mechanism by which kynurenine, a tryptophan-related metabolite, induces immune suppression remains poorly understood. Herein, we show that the increased production of kynurenine correlates with defective interleukin-2 (IL-2) signaling in memory CD4 T cells from HIV-infected subjects. Defective IL-2 signaling in these subjects, which drives reduced protection from Fas-mediated apoptosis, was also associated with memory CD4 T-cell loss. Treatment of memory CD4 T cells with the concentration of kynurenine found in plasma inhibited IL-2 signaling through the production of reactive oxygen species. We further show that IL-2 signaling in memory CD4 T cells is improved by the antioxidant N-acetylcysteine. Early initiation of antiretroviral therapy restored the IL-2 response in memory CD4 T cells by reducing reactive oxygen species and kynurenine production. The study findings provide a kynurenine-dependent mechanism through IL-2 signaling for reduced CD4 T-cell survival, which can be reversed by early treatment initiation in HIV-1 infection.

IMPORTANCE:

The persistence of functional memory CD4 T cells represents the basis for long-lasting immune protection in individuals after exposure to HIV-1. Unfortunately, primary HIV-1 infection results in the massive loss of these cells within weeks of infection, which is mainly driven by inflammation and massive infection by the virus. These new findings show that the enhanced production of kynurenine, a metabolite related to tryptophan catabolism, also impairs memory CD4 T-cell survival and interferes with IL-2 signaling early during HIV-1 infection.

PMID:
27356894
PMCID:
PMC4988137
DOI:
10.1128/JVI.00994-16
[Indexed for MEDLINE]
Free PMC Article

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