Article(id=1322923406383001943, tenantId=1146029695717560320, journalId=1255847919539208197, issueId=1322923268038078806, articleNumber=null, orderNo=null, doi=10.13193/j.issn.1673-7717.2025.04.026, 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=1793339118810, onlineDateStr=2026-10-30, pubDate=1744214400000, pubDateStr=2025-04-10, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1793339118810, onlineIssueDateStr=2026-10-30, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1793339118810, creator=13701087609, updateTime=1793339118810, 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=162, endPage=167, ext={EN=ArticleExt(id=1322923406886318424, articleId=1322923406383001943, tenantId=1146029695717560320, journalId=1255847919539208197, language=EN, title=Research Progress on Regulation of Tumor Infiltrating Lymphocytes by Traditional Chinese Medicine Monomers for Anti-Tumor Effects, columnId=1256183361521967297, journalTitle=Chinese Archives of Traditional Chinese Medicine, columnName=Target on National Project, runingTitle=null, highlight=null, articleAbstract=
Tumor infiltrating lymphocytes(TILs)therapy has become one of the most promising immunotherapies at present,and its advantages of good effect and low toxicity and side effects have made it more and more popular in clinical treatment. TILs are a kind of immune cells present in tumor tissues,which play the role of inhibiting tumor growth and specifically killing tumor cells by directly or indirectly participating in immune response. Traditional Chinese medicine(TCM)has a profound influence in the field of tumor therapy,and a large number of studies have shown that TCM monomers,such as mulberry huang polysaccharides,triptolide,artemisinin,glycyrrhizic acid and so on,directly or indirectly enhance the killing ability of immune cells against tumor cells by promoting the function of T cells,natural killer(NK)cells,or inhibiting the function of tumor-associated macrophage(TAMs),dendritic cells(DCs),myeloid-derived suppressor cells(MDSCs)and regulatory T cells(Tregs),which in turn exerts an anti-tumor effect. In this paper,it screened and summarized the research results on the anti-tumor effects of TCM monomers regulating TILs in recent years,and took TILs as the starting point to introduce in detail the mechanism of action of TCM monomers regulating TILs,with a view to promoting the research and development of new drugs for TCM monomers regulating TILs in anti-tumor,exploring the new ideas and methods of TCM in the field of tumor treatment and assisting the TCM to go towards the road of modernization successfully in the treatment of tumors.
, authors=Mingyang HE, Chengzhi WANG, Shan ZHANG, Dongdong LI, Peimin LIU, authorsList=Mingyang HE, Chengzhi WANG, Shan ZHANG, Dongdong LI, Peimin LIU, authorCompany=null, correspAuthors=Dongdong LI, Peimin LIU, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=null, pdf=null, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, abstractGraphContent=null, abstractVideo=null, citation=null, cebUrl=null, magXmlContent=null, mapNumber=null, fund=null), CN=ArticleExt(id=1322923410224984415, articleId=1322923406383001943, tenantId=1146029695717560320, journalId=1255847919539208197, language=CN, title=中药单体调控肿瘤浸润淋巴细胞抗肿瘤的研究进展, columnId=1256183362172142382, journalTitle=中华中医药学刊, columnName=国家项目点击, runingTitle=null, highlight=null, articleAbstract=
肿瘤浸润淋巴细胞(tumor infiltrating lymphocytes,TILs)免疫疗法已成为目前最具有潜力的免疫疗法之一,其效果好、不良反应小的优点,使其在临床治疗上越来越受欢迎。TILs是一种存在于肿瘤组织中的免疫细胞,通过直接或间接参与免疫反应,起到抑制肿瘤生长并特异性杀伤肿瘤细胞的作用。中医药在肿瘤治疗领域影响深远,大量研究表明,中药单体如桑黄多糖、雷公藤甲素、青蒿素、甘草酸等,通过促进T细胞、自然杀伤细胞(natural killer cell,NK)或抑制肿瘤相关巨噬细胞(tumor-associated macrophage,TAMs)、树突状细胞(dendritic cell,DC)、髓源抑制性细胞(myeloidderived suppressor cells,MDSCs)、调节性T细胞(regulatory T cells,Tregs)的功能,直接或间接增强免疫细胞对肿瘤细胞的杀伤能力,进而起到抗肿瘤作用。筛选总结近年来中药单体调控TILs抗肿瘤的研究成果,以TILs为着手点,详细介绍了中药单体调控TILs抗肿瘤的作用机制,以期促进中药单体调控TILs抗肿瘤的新药研发,开拓中医药在肿瘤治疗领域的新思路与新方法,助力中医药在肿瘤治疗中成功走向现代化之路。
, authors=赫名扬, 王成志, 张山, 李东东, 刘培民, authorsList=赫名扬, 王成志, 张山, 李东东, 刘培民, authorCompany=null, correspAuthors=李东东, 刘培民, authorNote=
赫名扬(1999-),男,河南开封人,硕士在读,研究方向:中医药防止恶性肿瘤。
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赫名扬(1999-),男,河南开封人,硕士在读,研究方向:中医药防止恶性肿瘤。
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赫名扬(1999-),男,河南开封人,硕士在读,研究方向:中医药防止恶性肿瘤。
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| 肿瘤浸润淋巴细胞 | 中药单体 | 来源 | 调节免疫方式 | 参考文献 |
|---|
| T细胞 | 芡茎多糖 | 芡茎 | 上调淋巴细胞亚群浸润能力,诱导Caspase-3凋亡通路 | [14] |
| 黄芪多糖 | 黄芪 | 联合5-FU降低CD4+T淋巴细胞的浸润能力,提高CD8+T淋巴细胞的浸润能力 | [15] |
| 灵芝多糖 | 灵芝 | 增强CD3+、CD8+T细胞的肿瘤浸润能力,提高T淋巴细胞肿瘤浸润 | [16] |
| 香菇多糖 | 香菇 | 联合腺病毒载体增加肿瘤组织浸润CD8+T细胞数量,促进IFN-β和IFN-γ的分泌 | [17] |
| 红景天乙醇提取物 | 红景天 | 增加肿瘤浸润的CD4+T细胞和CD8+T细胞数量 | [18] |
| 小檗碱 | 黄连 | 增强肿瘤浸润性T细胞免疫、减弱MDSC和Tregs的活化,降低肿瘤细胞中PD-L1的水平 | [19] |
| 川楝素 | 川楝子 | 增强T细胞浸润 | [20] |
| 淫羊藿苷 | 淫羊藿 | 上调的IFN-γ和TNF-α的细胞毒性CD8+T细胞浸润的表达 | [21] |
| 通关藤提取物 | 通关藤 | 增加CD3+/CD8+肿瘤浸润性T细胞密度 | [22] |
| 虫草素 | 虫草 | 抑制TSP1与CD47的结合,减少T细胞凋亡,促进生成大量T细胞向肿瘤浸润 | [23] |
| 黄芩苷 | 黄芩 | 提高CD4+T和CD8+T细胞向肿瘤的浸润 | [24] |
| 穿心莲内酯 | 穿心莲 | 提高CD8+T细胞浸润能力 | [25] |
| 淫羊藿苷 | 淫羊藿 | 增加CD8+T细胞浸润能力 | [26] |
| 白芍总苷 | 白芍 | 增加肿瘤浸润性CD4+和CD8+T细胞中T记忆干细胞和中枢记忆细胞数量 | [27] |
| 姜黄素 | 姜黄 | 上调CD4+和CD8+T细胞浸润的表达 | [29] |
| 隐丹参酮 | 丹参 | 促进TAMs和DC的活化,上调CD8+T细胞浸润能力 | [30] |
| 青蒿素 | 青蒿 | 促进抗肿瘤T细胞的浸润和增殖 | [31] |
| 龙葵多糖 | 龙葵 | 上调TNF-α、IFN-γ和IL-4的表达,下调IL-6的表达,增多浸润性T细胞数量 | [32] |
| 自然杀伤细胞 | 桑黄多糖 | 桑黄 | 增加NK细胞浸润能力 | [33] |
| 黄芪甲苷Ⅲ | 黄芪 | 提高NK细胞NKG2D、FAS和IFN-γ的表达,增加NK细胞向肿瘤的浸润 | [36] |
| 蝎毒 | 全蝎 | 上调肿瘤浸润性NK细胞、NKG2D蛋白、穿孔素和颗粒酶B mRNA的表达 | [37] |
| 人参总皂苷 | 人参 | 提高NK细胞在肿瘤组织浸润能力,上调穿孔素、颗粒酶B的mRNA表达,增加NK细胞数量 | [38] |
| 肿瘤相关巨噬细胞 | 丹参总酚酸 | 丹参 | 联合抗-PD-L1抑制髓源性巨噬细胞向肿瘤浸润 | [41] |
| 雷公藤甲素 | 雷公藤 | 调整肿瘤衍生的CXCL12表达来重塑免疫微环境,减少TAMs的浸润 | [42] |
| 丹参水提取物 | 丹参 | 抑制COX2的表达,下调肿瘤中PGE2的分泌,减弱TAMs的肿瘤内浸润 | [43] |
| 白芍总苷 | 白芍 | 降低炎症因子水平,抑制TAM的浸润 | [27] |
| YTE-17 | 云南藤黄 | 抑制TAMs的肿瘤内浸润 | [44] |
| 和厚朴酚 | 厚朴 | 调控CCL2/CCR2通路减少TAMs的肿瘤内浸润 | [45] |
| 蛇床子素 | 蛇床子 | 抑制M2巨噬细胞极化过程中MRC1、CCL22和TGF-β的表达 | [46] |
| 髓源抑制性细胞 | 淫羊藿次苷Ⅱ | 淫羊藿 | 抗PD-1减少MDSCs向肿瘤的浸润,促进ROS介导的SRC/ERK/STAT3信号通路失活 | [48] |
| 淫羊藿苷 | 淫羊藿 | 降低MDSCs浸润频率 | [26] |
| 调节性T细胞 | 甘草酸 | 甘草 | 下调FOXP3、GITR和CTLA4的表达,减弱免疫抑制能力 | [49] |
| 红景天苷 | 红景天 | 下调FOXP3的表达和FOXP3+Treg的比值,上调CD4+ T效应细胞的表达 | [50] |
| 灯盏乙素 | 灯盏花 | 抑制肿瘤坏死因子受体2的表达,减少浸润性Tregs的数量,上调CD8+T细胞的表达 | [51] |
), ArticleFig(id=1322923414335402375, tenantId=1146029695717560320, journalId=1255847919539208197, articleId=1322923406383001943, language=CN, label=表1, caption=
中药单体调控肿瘤浸润淋巴具体作用机制总结
, figureFileSmall=null, figureFileBig=null, tableContent=
| 肿瘤浸润淋巴细胞 | 中药单体 | 来源 | 调节免疫方式 | 参考文献 |
|---|
| T细胞 | 芡茎多糖 | 芡茎 | 上调淋巴细胞亚群浸润能力,诱导Caspase-3凋亡通路 | [14] |
| 黄芪多糖 | 黄芪 | 联合5-FU降低CD4+T淋巴细胞的浸润能力,提高CD8+T淋巴细胞的浸润能力 | [15] |
| 灵芝多糖 | 灵芝 | 增强CD3+、CD8+T细胞的肿瘤浸润能力,提高T淋巴细胞肿瘤浸润 | [16] |
| 香菇多糖 | 香菇 | 联合腺病毒载体增加肿瘤组织浸润CD8+T细胞数量,促进IFN-β和IFN-γ的分泌 | [17] |
| 红景天乙醇提取物 | 红景天 | 增加肿瘤浸润的CD4+T细胞和CD8+T细胞数量 | [18] |
| 小檗碱 | 黄连 | 增强肿瘤浸润性T细胞免疫、减弱MDSC和Tregs的活化,降低肿瘤细胞中PD-L1的水平 | [19] |
| 川楝素 | 川楝子 | 增强T细胞浸润 | [20] |
| 淫羊藿苷 | 淫羊藿 | 上调的IFN-γ和TNF-α的细胞毒性CD8+T细胞浸润的表达 | [21] |
| 通关藤提取物 | 通关藤 | 增加CD3+/CD8+肿瘤浸润性T细胞密度 | [22] |
| 虫草素 | 虫草 | 抑制TSP1与CD47的结合,减少T细胞凋亡,促进生成大量T细胞向肿瘤浸润 | [23] |
| 黄芩苷 | 黄芩 | 提高CD4+T和CD8+T细胞向肿瘤的浸润 | [24] |
| 穿心莲内酯 | 穿心莲 | 提高CD8+T细胞浸润能力 | [25] |
| 淫羊藿苷 | 淫羊藿 | 增加CD8+T细胞浸润能力 | [26] |
| 白芍总苷 | 白芍 | 增加肿瘤浸润性CD4+和CD8+T细胞中T记忆干细胞和中枢记忆细胞数量 | [27] |
| 姜黄素 | 姜黄 | 上调CD4+和CD8+T细胞浸润的表达 | [29] |
| 隐丹参酮 | 丹参 | 促进TAMs和DC的活化,上调CD8+T细胞浸润能力 | [30] |
| 青蒿素 | 青蒿 | 促进抗肿瘤T细胞的浸润和增殖 | [31] |
| 龙葵多糖 | 龙葵 | 上调TNF-α、IFN-γ和IL-4的表达,下调IL-6的表达,增多浸润性T细胞数量 | [32] |
| 自然杀伤细胞 | 桑黄多糖 | 桑黄 | 增加NK细胞浸润能力 | [33] |
| 黄芪甲苷Ⅲ | 黄芪 | 提高NK细胞NKG2D、FAS和IFN-γ的表达,增加NK细胞向肿瘤的浸润 | [36] |
| 蝎毒 | 全蝎 | 上调肿瘤浸润性NK细胞、NKG2D蛋白、穿孔素和颗粒酶B mRNA的表达 | [37] |
| 人参总皂苷 | 人参 | 提高NK细胞在肿瘤组织浸润能力,上调穿孔素、颗粒酶B的mRNA表达,增加NK细胞数量 | [38] |
| 肿瘤相关巨噬细胞 | 丹参总酚酸 | 丹参 | 联合抗-PD-L1抑制髓源性巨噬细胞向肿瘤浸润 | [41] |
| 雷公藤甲素 | 雷公藤 | 调整肿瘤衍生的CXCL12表达来重塑免疫微环境,减少TAMs的浸润 | [42] |
| 丹参水提取物 | 丹参 | 抑制COX2的表达,下调肿瘤中PGE2的分泌,减弱TAMs的肿瘤内浸润 | [43] |
| 白芍总苷 | 白芍 | 降低炎症因子水平,抑制TAM的浸润 | [27] |
| YTE-17 | 云南藤黄 | 抑制TAMs的肿瘤内浸润 | [44] |
| 和厚朴酚 | 厚朴 | 调控CCL2/CCR2通路减少TAMs的肿瘤内浸润 | [45] |
| 蛇床子素 | 蛇床子 | 抑制M2巨噬细胞极化过程中MRC1、CCL22和TGF-β的表达 | [46] |
| 髓源抑制性细胞 | 淫羊藿次苷Ⅱ | 淫羊藿 | 抗PD-1减少MDSCs向肿瘤的浸润,促进ROS介导的SRC/ERK/STAT3信号通路失活 | [48] |
| 淫羊藿苷 | 淫羊藿 | 降低MDSCs浸润频率 | [26] |
| 调节性T细胞 | 甘草酸 | 甘草 | 下调FOXP3、GITR和CTLA4的表达,减弱免疫抑制能力 | [49] |
| 红景天苷 | 红景天 | 下调FOXP3的表达和FOXP3+Treg的比值,上调CD4+ T效应细胞的表达 | [50] |
| 灯盏乙素 | 灯盏花 | 抑制肿瘤坏死因子受体2的表达,减少浸润性Tregs的数量,上调CD8+T细胞的表达 | [51] |
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