Article(id=1322923516328289193, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322923268038078806, articleNumber=null, orderNo=null, doi=10.13193/j.issn.1673-7717.2025.04.024, pmid=null, cstr=null, oa=null, hot=null, price=null, onlineType=0, articleFormat=0, articleType=null, articleTypeStr=null, receivedDate=null, receivedDateStr=null, revisedDate=null, revisedDateStr=null, acceptedDate=null, acceptedDateStr=null, onlineDate=1793339145022, onlineDateStr=2026-10-30, pubDate=1744214400000, pubDateStr=2025-04-10, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1793339145022, onlineIssueDateStr=2026-10-30, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1793339145022, creator=13701087609, updateTime=1793339145022, updator=13701087609, issue=Issue{id=1322923268038078806, tenantId=1146029695717560320, journalId=1255847919539208197, year='2025', volume='43', issue='4', pageStart='1', pageEnd='258', issueExtLink='null', onlineDate='null', pubDate='1744214400000', pubDateStr='2025-04-10', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=1, articleOrder=1, issueType=-1, specialIssue=0, createTime=1793339085826, creator='13701087609', updateTime=1793340586453, updator='13701087609', preIssue=null, nextIssue=null, articleTotal=null, ext={EN=IssueExt(id=1322929562572686061, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322923268038078806, language=EN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=), CN=IssueExt(id=1322929562572686062, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322923268038078806, language=CN, specialIssueTitle=, coverIllustrator=null, specialIssueEditor=, specialIssueAbout=)}, issueFiles=null, downloadFileDto=null}, startPage=149, endPage=154, ext={EN=ArticleExt(id=1322923516575753130, articleId=1322923516328289193, tenantId=1146029695717560320, journalId=1255847919539208197, language=EN, title=Research Progress on Mechanism of Chinese Traditional Medicine Polysaccharide Regulating Immune Cells against Lung Cancer, columnId=1256183361521967297, journalTitle=Chinese Archives of Traditional Chinese Medicine, columnName=Target on National Project, runingTitle=null, highlight=null, articleAbstract=
Lung cancer is one of the most common malignant tumors in the world,its morbidity and mortality rank first,and has become the number one killer threatening human life and health in the world. Traditional Chinese medicine is widely used in the comprehensive treatment of anti-lung cancer,and its curative effect is exact. As the most common active component of traditional Chinese medicine,traditional Chinese medicine polysaccharide has a prominent anti-tumor immune effect. A large number of studies have found that traditional Chinese medicine polysaccharides,such as Astragalus polysaccharides,Ginseng polysaccharide,Epimedium polysaccharides,Ganoderma lucidum polysaccharide,Achyranthes bidentata polysaccharides and Dendrobium polysaccharide,can improve the immune microenvironment of lung cancer tumors by regulating immune cells such as macrophages,dendritic cells,natural killer cells,myeloid suppressor cells,T cells and regulatory T cells to improve the function and activity of immune cells and enhance the body's immune response,so as to better play the role of anti-lung cancer. By collecting literatures on the anti-lung cancer effect of traditional Chinese medicine polysaccharides at home and abroad in recent years,this paper discussed the regulation of immune cells by traditional Chinese medicine polysaccharides and the specific mechanism of its anti-lung cancer effect,with a view to providing new ideas for the anti-lung cancer treatment of TCM as well as a new theoretical basis for the research and development of clinically related new drugs,and promoting the extensive clinical application of integrated traditional Chinese and western medicine in the treatment of lung cancer.
, authors=Chengzhi WANG
1, Yifan LIU
1, Xiaoqing ZHANG
2, Gelei ZHAO
1, Shan ZHANG
1, Peimin LIU
1, Dongdong LI
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肺癌是世界范围内最常见的恶性肿瘤之一,其发病率和病死率均居于首位,已成为威胁全球人类生命健康的头号杀手。中医药在抗肺癌综合治疗中应用广泛,疗效确切,中药多糖作为最常见的中药活性成分,具有较突出的抗肿瘤免疫作用。大量研究发现,中药多糖如黄芪多糖、人参多糖、淫羊藿多糖、灵芝多糖、牛膝多糖以及石斛多糖等可以通过调节肺癌肿瘤免疫微环境中的巨噬细胞、树突状细胞、自然杀伤细胞、髓系抑制细胞、T细胞以及调节性T细胞等免疫细胞,改善肺癌肿瘤免疫微环境,提高免疫细胞功能和活性,增强机体免疫应答反应,从而更好地发挥抗肺癌作用。通过收集近年来国内外中药多糖发挥抗肺癌治疗作用的相关文献,从中药多糖调节免疫细胞及其抗肺癌作用具体机制方面进行论述,以期为中医药在抗肺癌治疗方面提供新思路,为临床相关新药研发提供新的理论依据,促进中西医结合治疗肺癌在临床中的广泛应用。
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1, 刘一帆
1, 张晓青
2, 赵戈蕾
1, 张山
1, 刘培民
1, 李东东
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王成志(1998-),男,河南驻马店人,硕士在读,研究方向:中医药防治恶性肿瘤的临床及基础。
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26(1):499-505., articleTitle=Immunomodulatory effect of lentinan on aberrant T subsets and cytokines profile in non-small cell lung cancer patients, refAbstract=null)], funds=[Fund(id=1322923523882230761, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322923516328289193, awardId=82204981, language=CN, fundingSource=国家自然科学基金项目(82204981), fundOrder=null, country=null), Fund(id=1322923523945145322, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322923516328289193, awardId=STG-ZYX06-202145, language=CN, fundingSource=河南省特色骨干学科中医学学科建设项目(STG-ZYX06-202145), fundOrder=null, country=null), Fund(id=1322923524012254187, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322923516328289193, awardId=2021JDZX2002; 20-21ZY2115, language=CN, fundingSource=河南省中医药科学研究专项(2021JDZX2002; 20-21ZY2115), fundOrder=null, country=null), Fund(id=1322923524083557356, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322923516328289193, awardId=2022BSJJ07; 2023BSJJ02, language=CN, fundingSource=河南省中医院博士科研基金(2022BSJJ07; 2023BSJJ02), fundOrder=null, country=null), Fund(id=1322923524146471917, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322923516328289193, awardId=2022KYCX057; 2023KYCX043; 2023KYCX051, language=CN, fundingSource=河南中医药大学研究生科研创新能力提升计划项目(2022KYCX057; 2023KYCX043; 2023KYCX051), fundOrder=null, country=null)], companyList=[AuthorCompany(id=1322923519327216564, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322923516328289193, xref=1., ext=[AuthorCompanyExt(id=1322923519335605173, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322923516328289193, companyId=1322923519327216564, language=EN, country=null, province=null, city=null, postcode=null, companyName=null, departmentName=null, remark=
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| 免疫细胞 | 中药多糖 | 来源 | 调节免疫细胞具体作用机制 | 参考文献 |
|---|
| 巨噬细胞 | 黄芪多糖 | 黄芪 | 诱导M1/M2巨噬细胞极化,调节M1/M2巨噬细胞比例 促使M1巨噬细胞相关因子产生和分泌,增强MHC-Ⅱ分子表达 | [13] |
| 黄精多糖 | 黄精 | 调控AMPK/PDH轴,抑制M2巨噬细胞极化,促进巨噬细胞极化为M1型 | [14] |
| 淫羊藿多糖 | 淫羊藿 | 增加INF-γ、IL-6、TNF-α分泌 | [15] |
| | | 提高IL-2、INF-γ分泌,调整M1/M2巨噬细胞比例 | [16] |
| 香菇多糖 | 香菇 | 增加M1型巨噬细胞比例,降低M2型巨噬细胞的数量 增加IL-12、INF-γ表达,降低TGF-β表达 | [17] |
| 魔芋葡甘露聚糖 | 蛇六谷 | 降低Lewis肺癌小鼠血清内TGF-β、IL-10表达 | [18] |
| 茯苓多糖 | 茯苓 | 提高化疗后的肺癌小鼠体内IL-2、TNF-α表达 | [19] |
| 刺五加多糖 | 刺五加 | 上调TLR4信号通路,提高肺癌小鼠体内IL-1β、IL-6和TNF-α表达 | [20] |
| 白花蛇舌草多糖 | 白花蛇舌草 | 提高IL-2、TNF-α和IFN-γ表达,降低IL-10表达 | [21] |
| 莪术多糖 | 莪术 | 提高IL-2、TNF-α和IFN-γ表达,增强巨噬细胞的吞噬活性 | [22] |
| 灵芝多糖 | 灵芝 | 诱导IL-1α、IL-1β、IL-2、IFN-γ及TNF-α分泌和高表达 | [23] |
| 树突状细胞 | 车前子多糖 | 车前子 | 促进DC细胞成熟,增强DC细胞抗原处理和呈递能力,诱导IL-12分泌 | [28] |
| | | 激活MAPK和NF-κB信号通路,诱导DC细胞成熟 | [29] |
| 熟地黄多糖脂质体 | 熟地黄 | 提高MHCⅡ分子表达,促进DC细胞成熟 | [30] |
| 川牛膝多糖 | 川牛膝 | 诱导DC细胞抗原呈递到CD8+T细胞,激活细胞毒性T淋巴细胞免疫应答 诱导CD4+T淋巴细胞启动体液免疫 | [31] |
| 霍山石斛多糖 | 石斛 | 增加DC细胞数量,提高脾淋巴细胞增殖能力 | [32] |
| 自然杀伤细胞 | 山药多糖 | 山药 | 增加Lewis肺癌小鼠NK细胞数量 | [36] |
| 霍山石斛多糖 | 石斛 | 增加NK细胞数量 | [37] |
| 灵芝多糖 | 灵芝 | 增加TLR4缺陷小鼠NK细胞数量和杀伤活性 | [38] |
| 红花多糖 | 红花 | 增强NK细胞毒性作用 | [39] |
| 人参多糖 | 人参 | 上调NKp30、NKp44表达,诱导NK细胞活化 通过上调杀伤介质表达来提高NK细胞杀伤活性 | [40] |
| 髓系抑制细胞 | 黄芪多糖 | 黄芪 | 降低MDSCs比例,促进MDSCs分化成熟 | [44] |
| 人参多糖 | 人参 | 降低Arg-1、TGF-β、IL-10表达,提高IFN-γ、TNF-α表达,减少MDSCs数量 | [45] |
| 芦笋多糖 | 芦笋 | 抑制MDSCs增殖和活化 | [46] |
| | | 促进Caspase-9表达,抑制Bcl2表达,诱导MDSCs凋亡 | |
| T细胞 | 灵芝多糖 | 灵芝 | 增加CD4+/CD8+T细胞比例,促进INF-γ、IL-12分泌 | [49] |
| 黄芪多糖 | 黄芪 | 抑制TLR4/MyD88/NF-κB信号通路活化,提高CD3+、CD4+、CD8+比例 增加IL-2、IFN-γ表达,降低IL-4、IL-10表达,逆转Th1/Th2漂移 | [50] |
| | | 联合细胞因子诱导的杀伤细胞,上调机体CD3+、CD4+T淋巴细胞水平 | [51] |
| 人参多糖 | 人参 | 增加INF-γ、IL-2分泌,减少IL-4、IL-5分泌,维持Th1/Th2平衡 | [52] |
| | | 纠正Th1/Th2漂移现象 | [53] |
| 白花蛇舌草多糖 | 白花蛇舌草 | 提高CD3+T细胞、CD4+T细胞比例、降低CD8+T细胞比例,改善Th1/Th2漂移 | [54] |
| 芡茎多糖 | 芡茎 | 增加CD3+T细胞、CD4+T细胞比例,调节CD4+/CD8+T细胞比值 | [55] |
| 山豆根多糖 | 山豆根 | 提高CD4+T细胞、CD8+T细胞表达、CD4+/CD8+T细胞比值 | [56] |
| 调节性T细胞 | 人参多糖 | 人参 | 下调Arg-1、TGF-β、VEGF表达,上调INF-γ、TNF-α表达,减少Treg数量 | [45] |
| 灵芝多糖 | 灵芝 | 增加Teff/Treg细胞比例,降低Treg细胞对Teff增殖的抑制 | [60] |
| 香菇多糖 | 香菇 | 抑制Treg细胞增殖,降低CD4+ Treg细胞比例 | [61] |
), ArticleFig(id=1322923523785761768, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322923516328289193, language=CN, label=表1, caption=
中药多糖调节免疫细胞抗肺癌作用具体机制总结
, figureFileSmall=null, figureFileBig=null, tableContent=
| 免疫细胞 | 中药多糖 | 来源 | 调节免疫细胞具体作用机制 | 参考文献 |
|---|
| 巨噬细胞 | 黄芪多糖 | 黄芪 | 诱导M1/M2巨噬细胞极化,调节M1/M2巨噬细胞比例 促使M1巨噬细胞相关因子产生和分泌,增强MHC-Ⅱ分子表达 | [13] |
| 黄精多糖 | 黄精 | 调控AMPK/PDH轴,抑制M2巨噬细胞极化,促进巨噬细胞极化为M1型 | [14] |
| 淫羊藿多糖 | 淫羊藿 | 增加INF-γ、IL-6、TNF-α分泌 | [15] |
| | | 提高IL-2、INF-γ分泌,调整M1/M2巨噬细胞比例 | [16] |
| 香菇多糖 | 香菇 | 增加M1型巨噬细胞比例,降低M2型巨噬细胞的数量 增加IL-12、INF-γ表达,降低TGF-β表达 | [17] |
| 魔芋葡甘露聚糖 | 蛇六谷 | 降低Lewis肺癌小鼠血清内TGF-β、IL-10表达 | [18] |
| 茯苓多糖 | 茯苓 | 提高化疗后的肺癌小鼠体内IL-2、TNF-α表达 | [19] |
| 刺五加多糖 | 刺五加 | 上调TLR4信号通路,提高肺癌小鼠体内IL-1β、IL-6和TNF-α表达 | [20] |
| 白花蛇舌草多糖 | 白花蛇舌草 | 提高IL-2、TNF-α和IFN-γ表达,降低IL-10表达 | [21] |
| 莪术多糖 | 莪术 | 提高IL-2、TNF-α和IFN-γ表达,增强巨噬细胞的吞噬活性 | [22] |
| 灵芝多糖 | 灵芝 | 诱导IL-1α、IL-1β、IL-2、IFN-γ及TNF-α分泌和高表达 | [23] |
| 树突状细胞 | 车前子多糖 | 车前子 | 促进DC细胞成熟,增强DC细胞抗原处理和呈递能力,诱导IL-12分泌 | [28] |
| | | 激活MAPK和NF-κB信号通路,诱导DC细胞成熟 | [29] |
| 熟地黄多糖脂质体 | 熟地黄 | 提高MHCⅡ分子表达,促进DC细胞成熟 | [30] |
| 川牛膝多糖 | 川牛膝 | 诱导DC细胞抗原呈递到CD8+T细胞,激活细胞毒性T淋巴细胞免疫应答 诱导CD4+T淋巴细胞启动体液免疫 | [31] |
| 霍山石斛多糖 | 石斛 | 增加DC细胞数量,提高脾淋巴细胞增殖能力 | [32] |
| 自然杀伤细胞 | 山药多糖 | 山药 | 增加Lewis肺癌小鼠NK细胞数量 | [36] |
| 霍山石斛多糖 | 石斛 | 增加NK细胞数量 | [37] |
| 灵芝多糖 | 灵芝 | 增加TLR4缺陷小鼠NK细胞数量和杀伤活性 | [38] |
| 红花多糖 | 红花 | 增强NK细胞毒性作用 | [39] |
| 人参多糖 | 人参 | 上调NKp30、NKp44表达,诱导NK细胞活化 通过上调杀伤介质表达来提高NK细胞杀伤活性 | [40] |
| 髓系抑制细胞 | 黄芪多糖 | 黄芪 | 降低MDSCs比例,促进MDSCs分化成熟 | [44] |
| 人参多糖 | 人参 | 降低Arg-1、TGF-β、IL-10表达,提高IFN-γ、TNF-α表达,减少MDSCs数量 | [45] |
| 芦笋多糖 | 芦笋 | 抑制MDSCs增殖和活化 | [46] |
| | | 促进Caspase-9表达,抑制Bcl2表达,诱导MDSCs凋亡 | |
| T细胞 | 灵芝多糖 | 灵芝 | 增加CD4+/CD8+T细胞比例,促进INF-γ、IL-12分泌 | [49] |
| 黄芪多糖 | 黄芪 | 抑制TLR4/MyD88/NF-κB信号通路活化,提高CD3+、CD4+、CD8+比例 增加IL-2、IFN-γ表达,降低IL-4、IL-10表达,逆转Th1/Th2漂移 | [50] |
| | | 联合细胞因子诱导的杀伤细胞,上调机体CD3+、CD4+T淋巴细胞水平 | [51] |
| 人参多糖 | 人参 | 增加INF-γ、IL-2分泌,减少IL-4、IL-5分泌,维持Th1/Th2平衡 | [52] |
| | | 纠正Th1/Th2漂移现象 | [53] |
| 白花蛇舌草多糖 | 白花蛇舌草 | 提高CD3+T细胞、CD4+T细胞比例、降低CD8+T细胞比例,改善Th1/Th2漂移 | [54] |
| 芡茎多糖 | 芡茎 | 增加CD3+T细胞、CD4+T细胞比例,调节CD4+/CD8+T细胞比值 | [55] |
| 山豆根多糖 | 山豆根 | 提高CD4+T细胞、CD8+T细胞表达、CD4+/CD8+T细胞比值 | [56] |
| 调节性T细胞 | 人参多糖 | 人参 | 下调Arg-1、TGF-β、VEGF表达,上调INF-γ、TNF-α表达,减少Treg数量 | [45] |
| 灵芝多糖 | 灵芝 | 增加Teff/Treg细胞比例,降低Treg细胞对Teff增殖的抑制 | [60] |
| 香菇多糖 | 香菇 | 抑制Treg细胞增殖,降低CD4+ Treg细胞比例 | [61] |
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