Clermont Université, Université d'Auvergne, Unité de Nutrition Humaine, BP 10448, F-63000 Clermont-Ferrand, France; INRA, UMR 1019, UNH, CRNH Auvergne, F-63000 Clermont-Ferrand, France.
Centre Jean Perrin, Service de Statistiques, F-63000 Clermont-Ferrand, France.
Clin Nutr. 2015 Oct;34(5):810-7. doi: 10.1016/j.clnu.2014.12.002. Epub 2014 Dec 9.
Immunonutrition has been reported to improve the immune status of perioperative cancer patients, thereby reducing complications and length of hospital stay.
This study aimed to assess whether immunonutrition enriched in arginine, EPA & DHA and nucleotides could impact the immune cells responses in head & neck and esophageal cancer patients treated by radiochemotherapy (RCT).
A double-blind clinical trial was carried out in 28 patients randomized into two groups, receiving either an immunomodulating enteral nutrition formula (IEN, n = 13, Impact(®), Nestlé) or an isoenergetic isonitrogenous standard enteral nutrition formula (SEN, n = 15) throughout RCT (5-7 weeks). After isolation from whole blood, immune cells metabolism and functions were assessed at the beginning (Db) and at the end (De) of RCT.
Immunonutrition maintained CD4(+)/CD8(+) T-lymphocyte counts ratio and CD3 membrane expression between Db and De. Polymorphonuclear cells CD62L and CD15 densities and ROS production were increased in IEN patients. Peripheral blood mononuclear cells (PBMC) production of pro-inflammatory prostaglandin-E2 was stable in IEN patients and lower than in SEN patients at De. Genes coding for immune receptors, antioxidant enzymes and NADPH oxidase subunits were overexpressed in the PBMC of IEN vs SEN patients at De.
Immunonutrition can enhance immune cell responses through the modulation of their phenotypes and functions. By modulating the gene expression of immune cells, immunonutrition could make it easier for the organism to adapt to the systemic inflammation and oxidative stress induced by RCT.
This clinical trial has been registered on ClinicalTrial.gov website: NCT00333099.
免疫营养已被报道可改善围手术期癌症患者的免疫状态,从而减少并发症和住院时间。
本研究旨在评估富含精氨酸、EPA 和 DHA 以及核苷酸的免疫营养是否会影响接受放化疗(RCT)的头颈部和食管癌患者的免疫细胞反应。
对 28 例患者进行了一项双盲临床试验,随机分为两组,分别接受免疫调节型肠内营养配方(IEN,n=13,Impact®,雀巢)或等能量等氮标准肠内营养配方(SEN,n=15)在 RCT 期间(5-7 周)。在 RCT 开始(Db)和结束(De)时,从全血中分离免疫细胞后,评估其代谢和功能。
免疫营养维持了 CD4+/CD8+T 淋巴细胞计数比和 CD3 膜表达在 Db 和 De 之间。IEN 患者的多形核细胞 CD62L 和 CD15 密度和 ROS 产生增加。IEN 患者外周血单核细胞(PBMC)产生的促炎前列腺素-E2 在 IEN 患者中保持稳定,且低于 SEN 患者在 De 时的水平。在 De 时,IEN 与 SEN 患者相比,PBMC 中免疫受体、抗氧化酶和 NADPH 氧化酶亚基的编码基因表达上调。
免疫营养可通过调节免疫细胞的表型和功能来增强免疫细胞反应。通过调节免疫细胞的基因表达,免疫营养可以使机体更容易适应 RCT 引起的全身炎症和氧化应激。
该临床试验已在 ClinicalTrials.gov 网站上注册:NCT00333099。