Center for Infectious Diseases, Stony Brook University, Stony Brook, NY 11794-5120, USA.
Cell Host Microbe. 2012 Dec 13;12(6):791-8. doi: 10.1016/j.chom.2012.10.018.
Salmonella enterica serovar Typhimurium avoids clearance by the host immune system by suppressing T cell responses; however, the mechanisms that mediate this immunosuppression remain unknown. We show that S. Typhimurium inhibit T cell responses by producing L-Asparaginase II, which catalyzes the hydrolysis of L-asparagine to aspartic acid and ammonia. L-Asparaginase II is necessary and sufficient to suppress T cell blastogenesis, cytokine production, and proliferation and to downmodulate expression of the T cell receptor. Furthermore, S. Typhimurium-induced inhibition of T cells in vitro is prevented upon addition of L-asparagine. S. Typhimurium lacking the L-Asparaginase II gene (STM3106) are unable to inhibit T cell responses and exhibit attenuated virulence in vivo. L-Asparaginases are used to treat acute lymphoblastic leukemia through mechanisms that likely involve amino acid starvation of leukemic cells, and these findings indicate that pathogens similarly use L-asparagine deprivation to limit T cell responses.
肠炎沙门氏菌血清型 Typhimurium 通过抑制 T 细胞应答来逃避宿主免疫系统的清除;然而,介导这种免疫抑制的机制尚不清楚。我们表明,沙门氏菌 Typhimurium 通过产生 L-天冬酰胺酶 II 来抑制 T 细胞反应,L-天冬酰胺酶 II 催化 L-天冬酰胺水解为天冬氨酸和氨。L-天冬酰胺酶 II 是抑制 T 细胞有丝分裂、细胞因子产生、增殖和下调 T 细胞受体表达所必需和充分的。此外,在添加 L-天冬酰胺后,可防止体外沙门氏菌 Typhimurium 诱导的 T 细胞抑制。缺乏 L-天冬酰胺酶 II 基因(STM3106)的沙门氏菌 Typhimurium 无法抑制 T 细胞反应,并且在体内的毒力减弱。L-天冬酰胺酶用于通过可能涉及白血病细胞氨基酸饥饿的机制治疗急性淋巴细胞白血病,这些发现表明病原体同样通过剥夺 L-天冬酰胺来限制 T 细胞反应。