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The effect of l-arginine supplementation and surgical trauma on the frequency of myeloid-derived suppressor cells and T lymphocytes in tumour and blood of colorectal cancer patients

医学 免疫抑制 安慰剂 髓源性抑制细胞 结直肠癌 内科学 免疫系统 胃肠病学 癌症 抑制器 免疫学 病理 替代医学
作者
Jarosław Szefel,Tomasz Ślebioda,Jakub Walczak,Wiesław Janusz Kruszewski,Mariusz Szajewski,Maciej Ciesielski,Marcin Stanisławowski,Tomasz Buczek,Sylwia Małgorzewicz,Anna Owczarzak,Ewa Aleksandrowicz‐Wrona,Grzegorz Krzykowski
出处
期刊:Advances in Medical Sciences [Elsevier BV]
卷期号:67 (1): 66-78 被引量:16
标识
DOI:10.1016/j.advms.2021.12.005
摘要

l-arginine (L-arg) deficiency causes immunosuppression, but it is unknown if L-arg supplementation in colorectal cancer (CRC) patients restores immune system activity. Our objective was to investigate the effect of L-arg supplementation on the frequency of monocytic (M) and polymorphonuclear (PNM) myeloid-derived suppressor cells (M-MDSCs and PMN-MDSCs, respectively).We enrolled 65 CRC patients (34 males, 31 females) aged 69 ​± ​10 years into a prospective, randomised, double-blind study. Twenty-eight patients received L-arg and 37 received placebo for 9 days at a dose of 10 ​g/day. The frequency changes in MDSC, CD4+ cells and the concentration of C-reactive protein (CRP) were assessed before supplementation with L-arg (test 1), after 9 days of supplementation (test 2), and after surgery on day 11 (test 3).The frequency of M-MDSC in the tumours of patients receiving L-arg supplementation was higher than in placebo-treated patients, as was the frequency of PMN-MDSC and M-MDSC in the mucosa. CRP concentration in the serum of placebo-treated patients in test 2 was higher than in test 1, and the concentration in the serum of patients with L-arg supplementation in test 2 was lower than in test 1. Moreover, the expression pattern of the argininosuccinate synthase 1 (ASS1) suggests that CRC is not auxotrophic for L-arg.The results of this study do not support the hypothesis that L-arg supplementation in CRC patients can reduce immunosuppression by decreasing the frequency of suppressor cells and increasing the frequency of effector CD4+ T cells.
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