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10.3389/fimmu.2017.01561

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suck abstract from ncbi


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pmid29201027
      Front+Immunol 2017 ; 8 (ä): 1561
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  • l-Citrulline Metabolism in Mice Augments CD4(+) T Cell Proliferation and Cytokine Production In Vitro, and Accumulation in the Mycobacteria-Infected Lung #MMPMID29201027
  • Lange SM ; McKell MC ; Schmidt SM ; Hossfeld AP ; Chaturvedi V ; Kinder JM ; McAlees JW ; Lewkowich IP ; Way SS ; Turner J ; Qualls JE
  • Front Immunol 2017[]; 8 (ä): 1561 PMID29201027 show ga
  • Activation, recruitment, and effector function of T lymphocytes are essential for control of mycobacterial infection. These processes are tightly regulated in T cells by the availability of l-arginine within the microenvironment. In turn, mycobacterial infection dampens T cell responsiveness through arginase induction in myeloid cells, promoting sequestration of l-arginine within the local milieu. Here, we show T cells can replenish intracellular l-arginine through metabolism of l-citrulline to mediate inflammatory function, allowing anti-mycobacterial T cells to overcome arginase-mediated suppression. Furthermore, T cell l-citrulline metabolism is necessary for accumulation of CD4(+) T cells at the site of infection, suggesting this metabolic pathway is involved during anti-mycobacterial T cell immunity in vivo. Together, these findings establish a contribution for l-arginine synthesis by T cells during mycobacterial infection, and implicate l-citrulline as a potential immuno-nutrient to modulate host immunity.
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