1.西安交通大学附属三二〇一医院肿瘤内科(陕西 汉中 723000)
2.西安交通大学第一附属医院肝胆外科(陕西 西安 710061)
姚忠强,男,硕士,副主任医师,主要从事中西医结合肿瘤临床与研究工作
王娟毅,主任医师;E-mail:doctorwxn@163.com
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姚忠强,王斐斐,李炜等.葛根芩连汤加减对结直肠癌患者炎症因子和免疫细胞水平影响的临床研究[J].上海中医药杂志,2022,56(7):48-52.
YAO Zhongqiang,WANG Feifei,LI Wei,et al.Effect of modified Gegen Qinlian Decoction on inflammatory factors and immune cells in patients with colorectal cancer[J].Shanghai Journal of Traditional Chinese Medicine,2022,56(7):48-52.
姚忠强,王斐斐,李炜等.葛根芩连汤加减对结直肠癌患者炎症因子和免疫细胞水平影响的临床研究[J].上海中医药杂志,2022,56(7):48-52. DOI: 10.16305/j.1007-1334.2022.2203002.
YAO Zhongqiang,WANG Feifei,LI Wei,et al.Effect of modified Gegen Qinlian Decoction on inflammatory factors and immune cells in patients with colorectal cancer[J].Shanghai Journal of Traditional Chinese Medicine,2022,56(7):48-52. DOI: 10.16305/j.1007-1334.2022.2203002.
目的,2,观察葛根芩连汤加减对结直肠癌患者炎症因子和免疫细胞水平的影响。,方法,2,将82例拟行手术治疗的结直肠癌患者随机分为对照组和治疗组,每组41例,对照组予常规治疗和限期手术,治疗组在此基础上于手术前7 d开始服用葛根芩连汤加减方。比较两组血浆免疫细胞[CD4,+, T细胞、CD8,+, T细胞、自然杀伤(NK)细胞、自然杀伤T(NKT)细胞、调节性T(Treg)细胞)]和炎症因子[肿瘤坏死因子-α(TNF-α)、γ干扰素(IFN-γ)、白介素-2(IL-2)、白介素-6(IL-6)、白介素-10(IL-10)、5-羟色胺(5-HT)]水平,以及肿瘤组织中5-HT、TNF-α表达的变化情况。,结果,2,①治疗前后组内比较,治疗组血浆CD4,+ ,T细胞、NKT细胞水平升高(,P,<,0.05),对照组血浆CD4,+ ,T细胞、NKT细胞、CD8,+ ,T细胞、NK细胞、Treg细胞水平差异均无统计学意义(,P,>,0.05);组间治疗后比较,治疗组CD4,+ ,T细胞、NKT细胞水平高于对照组(,P,<,0.05)。②治疗前后组内比较,治疗组血浆TNF-α、IFN-γ、IL-2、IL-6、IL-10、5-HT水平降低(,P,<,0.05),对照组上述炎症因子水平差异均无统计学意义(,P,>,0.05);组间治疗后比较,治疗组血浆TNF-α、IFN-γ、IL-2、IL-6、IL-10、5-HT水平低于对照组(,P,<,0.05)。③术后与治疗前组内比较,治疗组肿瘤组织中TNF-α、5-HT的累积光密度(IOD)值降低(,P,<,0.05),对照组肿瘤组织中TNF-α、5-HT的IOD值差异无统计学意义(,P,>,0.05);组间术后比较,治疗组肿瘤组织中TNF-α、5-HT的IOD值低于对照组(,P,<,0.05)。,结论,2,葛根芩连汤加减治疗可有效调节结直肠癌患者的免疫水平和炎症反应,具有良好的临床应用前景。
Objective,2,To investigate the effect of Modified Gegen Qinlian Decoction (MGQD) on inflammatory factors and immune cells in patients with colorectal cancer.,Methods,2,A total of 82 patients with colorectal cancer to be treated by operation were randomly divided into a control group (,n,=41) and a treatment group (,n,=41). Both groups were administered with conventional treatment and confine operation, and the treatment group was additionally administered with MGQD 7 days before operation. The changes of immune cells [CD4,+,T cells, CD8,+,T cells, natural killer (NK) cells, natural killer T (NKT) cells, and Treg cells] and inflammatory factors [tumor necrosis factor-α (TNF-α), interferon-gamma (IFN-γ), interleukin-2 (IL-2), interleukin-6 (IL-6), interleukin-10 (IL-10), and 5-hydroxytryptamine (5-HT)] levels in plasma, as well as the changes of 5-HT and TNF-α expression in tumor tissues were compared between the two groups.,Results,2,①After treatment, the plasma levels of CD4,+, T cells and NKT cells in the treatment group increased (,P,<,0.05), but there was no significant difference in the plasma levels of CD4,+, T cells, NKT cells, CD8,+, T cells, NK cells and Treg cells before and after treatment in the control group (,P,>,0.05); After treatment, the levels of CD4,+, T cells and NKT cells in the treatment group were higher than those in the control group (,P,<,0.05). ②According to the intra-group comparison before and after treatment, the plasma levels of TNF-α, IFN-γ, IL-2, IL-6, IL-10, and 5-HT decreased in the treatment group (,P,<,0.05), but the differences in the levels of the above inflammatory factors in the control group were not statistically significant (,P,>,0.05); According to the inter-group comparison after treatment, the plasma levels of TNF-α, IFN-γ, IL-2, IL-6, IL-10, and 5-HT in the treatment group were lower than those in the control group (,P,<,0.05). ③The intra-group comparison before and after treatment showed that the IOD values of TNF-α and 5-HT in the tumor tissues of the treatment group decreased (,P,<,0.05), but there was no significant difference in IOD values of TNF-α and 5-HT in the tumor tissues of the control group (,P,>,0.05); The inter-group comparison after treatment showed that the IOD values of TNF-α and 5-HT in the tumor tissues of the treatment group were lower than those of the control group (,P,<,0.05).,Conclusion,2,The application of MGQD is promising in the clinic as it can effectively regulate the immune level and inflammatory response in colorectal cancer patients.
结直肠癌葛根芩连汤免疫调节炎症因子中医药疗法临床试验
colorectal cancerGegen Qinlian Decoctionimmunoregulationinflammatory factortraditional Chinese medicine therapyclinical trial
SIEGEL R L, MILLER K D, JEMAL A. Cancer statistics, 2020[J]. CA Cancer J Clin, 2020, 70 (1): 7-30.
中华人民共和国卫生和计划生育委员会医政医管局,中华医学会肿瘤学分会. 中国结直肠癌诊疗规范(2017年版)[J]. 中国医学前沿杂志(电子版),2018, 10(3): 1-21.
FENG Z, YANG R, WU L, et al. Atractylodes macrocephala polysaccharides regulate the innate immunity of colorectal cancer cells by modulating the TLR4 signaling pathway[J]. Onco Targets Ther, 2019, 12: 7111-7121.
FENG Z, YANG R, WU L, et al. Characterization of circulating T-, NK-, and NKT cell subsets in patients with colorectal cancer: the peripheral blood immune cell profile[J]. Cancer Immunol Immunother, 2019, 68(6): 1011-1024.
钱雨凡,刘宇婧,陆璐,等. 中医药调节结直肠癌免疫微环境的研究进展[J]. 上海中医药大学学报,2021, 35(4): 94-100.
王晓炜,张慈安,修丽娟,等. 316例结直肠癌前病变患者中医证型分布规律及肠镜下切除术后转归的回顾性研究[J]. 上海中医药杂志,2022, 56(2): 30-33.
LV J, JIA Y, LI J, et al. Gegen Qinlian decoction enhances the effect of PD-1 blockade in colorectal cancer with microsatellite stability by remodelling the gut microbiota and the tumour microenvironment[J]. Cell Death Dis, 2019, 10(6): 415.
刘荫华,徐玲. 第七版《AJCC肿瘤分期手册》结直肠癌内容的更新与解读[J]. 中华胃肠外科杂志,2010, 13(8): 629-631.
中华人民共和国国家卫生健康委员会. 中国结直肠癌诊疗规范(2020版)[J]. 中华消化外科杂志,2020, 19(6): 563-588.
WANG N, FENG Y, CHEUNG F, et al. A Chinese medicine formula Gegen Qinlian decoction suppresses expansion of human renal carcinoma with inhibition of matrix metalloproteinase-2[J]. Integr Cancer Ther, 2015, 14(1): 75-85.
BRAILEY P M, LEBRUSANT-FERNANDEZ M, BARRAL P. NKT cells and the regulation of intestinal immunity: a two-way street[J]. FEBS J, 2020, 287(9): 1686-1699.
MORANDI F, YAZDANIFAR M, COCCO C, et al. Engineering the bridge between innate and adaptive immunity for cancer immunotherapy: Focus on γδ T and NK cells[J]. Cells, 2020, 9(8): 1757.
MOSSANEN J C, KOHLHEPP M, WEHR A, et al. CXCR6 inhibits hepatocarcinogenesis by promoting natural killer T- and CD4+ T-cell-dependent control of senescence[J]. Gastroenterology, 2019, 156(6): 1877-1889.
IHARA F, SAKURAI D, TAKAMI M, et al. Regulatory T cells induce CD4- NKT cell anergy and suppress NKT cell cytotoxic function[J]. Cancer Immunol Immunother, 2019, 68(12): 1935-1947.
SHI Y, XU H, XIAO Y, et al. Gegen Qinlian decoction downregulates the TLR7 signalling pathway to control influenza A virus infection[J]. Biomed Pharmacother, 2020, 121: 109471.
WU Y, WANG D, YANG X, et al. Traditional Chinese medicine Gegen Qinlian decoction ameliorates irinotecan chemotherapy-induced gut toxicity in mice[J]. Biomed Pharmacother, 2019, 109: 2252-2261.
FAN Y, YI W, HUANG H, et al. Efficacy of herbal medicine (Gegen Qinlian Decoction) on ulcerative colitis: A systematic review of randomized controlled trials[J]. Medicine, 2019, 98(52): e18512.
LIU C S, LIANG X, WEI X H, et al. Gegen Qinlian decoction treats diarrhea in piglets by modulating gut microbiota and short-chain fatty acids[J]. Front Microbiol, 2019, 10: 825.
惠怡华,王海娜,苏文. 自然杀伤(NK)细胞表面受体表达谱及其功能的研究进展[J]. 细胞与分子免疫学杂志,2020, 36(8): 72-76.
XIA Z, ZHANG Y, LI C, et al. Traditional Tibetan medicine Anzhijinhua San attenuates ovalbumin-induced diarrhea by regulating the serotonin signaling system in mice[J]. J Ethnopharmacol, 2019, 236: 484-494.
孙御芳,倪中亚,王莉新,等. 基于NK细胞的肿瘤免疫逃逸及中医药对NK的免疫调节作用[J]. 中国医药导报,2019, 16(28): 52-55.
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