Article(id=1321501167268508052, tenantId=1146029695717560320, journalId=1246415837536497731, issueId=1321500868936052946, articleNumber=PA20260310_rGUflhEz, orderNo=null, doi=10.12307/2025.565, 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=1735315200000, acceptedDateStr=2024-12-28, onlineDate=1748534400000, onlineDateStr=2025-05-30, pubDate=1767801600000, pubDateStr=2026-01-08, doiRegisterDate=null, doiRegisterDateStr=null, onlineIssueDate=1793000030581, onlineIssueDateStr=2026-10-26, onlineJustAcceptDate=null, onlineJustAcceptDateStr=null, onlineFirstDate=null, onlineFirstDateStr=null, sourceXml=null, magXml=null, createTime=1793000030581, creator=admin, updateTime=1793000030581, updator=admin, issue=Issue{id=1321500868936052946, tenantId=1146029695717560320, journalId=1246415837536497731, year='2026', volume='30', issue='1', pageStart='null', pageEnd='null', issueExtLink='null', onlineDate='null', pubDate='1767801600000', pubDateStr='2026-01-08', beforeIssueId=null, nextIssueId=null, price=null, status=1, issueComplete=0, articleOrder=1, issueType=-1, specialIssue=null, createTime=1792999959453, creator='ztmeta', updateTime=1792999959453, updator='ztmeta', preIssue=null, nextIssue=null, articleTotal=null, ext=null, issueFiles=null, downloadFileDto=null}, startPage=248, endPage=259, ext={EN=ArticleExt(id=1321501169327911319, articleId=1321501167268508052, tenantId=1146029695717560320, journalId=1246415837536497731, language=EN, title=Targeting diverse chimeric antigen receptor T cell-related targets in treatment of B-cell hematological malignancies: a review of long-term follow-up data, columnId=null, journalTitle=Chinese Journal of Tissue Engineering Research, columnName=null, runingTitle=null, highlight=null, articleAbstract=BACKGROUND: Chimeric antigen receptor T cell therapy is a cutting-edge approach for the treatment of B cell hematological malignancies. These cells efficiently and specifically recognize and kill tumor cells, unrestricted by major histocompatibility complex limitations. OBJECTIVE: To elucidate the structure, developmental history, and marketed progress of chimeric antigen receptor T cells, summarize their long-term efficacy in B cell hematological malignancies treatments, and discuss associated toxicities, recurrence, and mitigation strategies. Additionally, it reviews the advancement of potential targets in B cell hematological malignancies treatments. METHODS: Searches were conducted in PubMed, CNKI, and WanFang databases using the terms “CAR-T, B cell hematological malignancies, toxic side effects, immunotherapy” in Chinese and English, focusing on articles regarding chimeric antigen receptor T cell targets in B-cell malignant tumor treatments. RESULTS AND CONCLUSION: (1) The U.S. Food and Drug Administration and National Medical Products Administration have approved 11 chimeric antigen receptor T cell products, primarily targeting CD19 and B cell maturation antigen targets in B cell hematological malignancies. (2) Long-term follow-up data indicate that chimeric antigen receptor T cell therapy provides a high remission rate and enduring responses in B cell hematological malignancies patients, albeit with recurrence issues due to antigen loss or downregulation. (3) Chimeric antigen receptor T cell therapy is associated with significant toxicities, a high recurrence rate, and drug resistance, constraining its broad application. (4) Future research should concentrate on developing new targets, combined therapies, and strategies to enhance chimeric antigen receptor T cell persistence and antitumor activity., authors=null, authorsList=null, authorCompany=null, correspAuthors=null, 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=1321501169260802454, articleId=1321501167268508052, tenantId=1146029695717560320, journalId=1246415837536497731, language=CN, title=不同嵌合抗原受体T细胞相关靶点治疗B细胞血液恶性肿瘤:长期随访数据综述, columnId=null, journalTitle=中国组织工程研究, columnName=null, runingTitle=null, highlight=null, articleAbstract=背景:嵌合抗原受体T (chimeric antigen receptor T,CAR-T)细胞疗法是治疗B细胞血液恶性肿瘤的前沿方法,其能高效且特异性地识别并杀伤肿瘤细胞,不受主要组织相容性复合体限制。 目的:旨在梳理CAR-T细胞的结构、发展历程及上市产品进展,总结CAR-T细胞治疗B细胞血液恶性肿瘤的长期疗效,并探讨治疗后的毒副作用、复发性及解决策略,同时综述潜在靶点治疗B细胞血液恶性肿瘤的进展。 方法:以“嵌合抗原受体T细胞,B细胞恶性肿瘤,毒副作用,免疫疗法”为中文检索词,以“CAR-T、B cell hematological malignancies,Toxic side effects,Immunotherapy”为英文检索词在中国知网、万方数据库、PubMed数据库检索CAR-T细胞相关靶点治疗B细胞恶性肿瘤的文献。 结果与结论:①美国食品药品监督管理局和中国国家药品监督管理局共批准11款CAR-T细胞产品,主要针对B细胞血液恶性肿瘤的CD19和B细胞成熟抗原靶点;②长期随访数据显示,CAR-T细胞治疗为B细胞血液恶性肿瘤患者带来高缓解率和持久反应,但存在抗原丢失或下调导致的复发问题;③CAR-T细胞治疗存在高毒副作用、高复发率和耐药性等问题,限制了其广泛应用;④未来研究的方向包括开发新的靶点、联合治疗等策略,以提高CAR-T细胞的持久性和抗肿瘤活性。, authors=null, authorsList=null, authorCompany=null, correspAuthors=null, authorNote=null, correspAuthorsNote=null, copyrightStatement=null, copyrightOwner=null, extLink=null, articleAbsUrl=null, sourceXml=null, magXml=null, pdfUrl=https://oss.bj-dx-dzqywjd-hlw-icp.inspurcloudoss.com:6063/cast-journal-prod/2030916229985292289/excel/pdfs/36fff1fe87bc4ea3846dbc9abcde3aa8.pdf?response-content-disposition=attachment%3B%20filename%3D%22%E4%B8%8D%E5%90%8C%E5%B5%8C%E5%90%88%E6%8A%97%E5%8E%9F%E5%8F%97%E4%BD%93T%E7%BB%86%E8%83%9E%E7%9B%B8%E5%85%B3%E9%9D%B6%E7%82%B9%E6%B2%BB%E7%96%97B%E7%BB%86%E8%83%9E%E8%A1%80%E6%B6%B2%E6%81%B6%E6%80%A7%E8%82%BF%E7%98%A4%EF%BC%9A%E9%95%BF%E6%9C%9F%E9%9A%8F%E8%AE%BF%E6%95%B0%E6%8D%AE%E7%BB%BC%E8%BF%B0.pdf%22&X-Amz-Algorithm=AWS4-HMAC-SHA256&X-Amz-Date=20261026T073155Z&X-Amz-SignedHeaders=host&X-Amz-Expires=604800&X-Amz-Credential=NjRlNmUzOGMtM2Y3OC00MDQ3LThkMmYtN2JkODRmYmI3MTgw%2F20261026%2Fbj-dx-dzqywjd-hlw-icp%2Fs3%2Faws4_request&X-Amz-Signature=499fea20d138b8eed8bce75b3debadc11d323bddafb3ceb47114a7388de8c71d, pdf=Dl7dyIRseoq8sF8exiUuMQ==, pdfFileSize=null, pdfExtLink=null, richHtmlUrl=null, mobilePdfUrl=null, reviewReport=null, pdfFirstPage=null, abstractGraph=null, 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tenantId=1146029695717560320, journalId=1246415837536497731, articleId=1321501167268508052, language=EN, orderNo=5, keyword=long-term efficacy), Keyword(id=1321501175539675570, tenantId=1146029695717560320, journalId=1246415837536497731, articleId=1321501167268508052, language=EN, orderNo=6, keyword=toxic side effects), Keyword(id=1321501175929745843, tenantId=1146029695717560320, journalId=1246415837536497731, articleId=1321501167268508052, language=EN, orderNo=7, keyword=recurrence)], refs=[Reference(id=1321501177670382008, tenantId=1146029695717560320, journalId=1246415837536497731, articleId=1321501167268508052, doi=null, pmid=null, pmcid=null, year=null, volume=null, issue=null, pageStart=null, pageEnd=null, url=null, language=null, rfNumber=[1], rfOrder=0, authorNames=null, journalName=null, refType=null, unstructuredReference=TIMMERS M, ROEX G, WANG Y, et al. 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不同嵌合抗原受体T细胞相关靶点治疗B细胞血液恶性肿瘤:长期随访数据综述
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许凡萍 1, , 李勤椿 1, , 唐冬芳 1,
中国组织工程研究 | 2026,30(1): 248-259
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中国组织工程研究 2026 , 30 (1) : 248 -259
不同嵌合抗原受体T细胞相关靶点治疗B细胞血液恶性肿瘤:长期随访数据综述
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许凡萍1, , 李勤椿1,, 唐冬芳1,
作者信息
  • 1.南科技学院,湖南省永州市 425199
  • 2.南科技学院,湖南省永州市 425199
Targeting diverse chimeric antigen receptor T cell-related targets in treatment of B-cell hematological malignancies: a review of long-term follow-up data
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出版时间: 2026-01-08 doi: 10.12307/2025.565
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背景:嵌合抗原受体T (chimeric antigen receptor T,CAR-T)细胞疗法是治疗B细胞血液恶性肿瘤的前沿方法,其能高效且特异性地识别并杀伤肿瘤细胞,不受主要组织相容性复合体限制。 目的:旨在梳理CAR-T细胞的结构、发展历程及上市产品进展,总结CAR-T细胞治疗B细胞血液恶性肿瘤的长期疗效,并探讨治疗后的毒副作用、复发性及解决策略,同时综述潜在靶点治疗B细胞血液恶性肿瘤的进展。 方法:以“嵌合抗原受体T细胞,B细胞恶性肿瘤,毒副作用,免疫疗法”为中文检索词,以“CAR-T、B cell hematological malignancies,Toxic side effects,Immunotherapy”为英文检索词在中国知网、万方数据库、PubMed数据库检索CAR-T细胞相关靶点治疗B细胞恶性肿瘤的文献。 结果与结论:①美国食品药品监督管理局和中国国家药品监督管理局共批准11款CAR-T细胞产品,主要针对B细胞血液恶性肿瘤的CD19和B细胞成熟抗原靶点;②长期随访数据显示,CAR-T细胞治疗为B细胞血液恶性肿瘤患者带来高缓解率和持久反应,但存在抗原丢失或下调导致的复发问题;③CAR-T细胞治疗存在高毒副作用、高复发率和耐药性等问题,限制了其广泛应用;④未来研究的方向包括开发新的靶点、联合治疗等策略,以提高CAR-T细胞的持久性和抗肿瘤活性。
B细胞血液恶性肿瘤  /  嵌合抗原受体T细胞  /  免疫疗法  /  治疗靶点  /  长期疗效  /  毒副作用  /  复发
BACKGROUND: Chimeric antigen receptor T cell therapy is a cutting-edge approach for the treatment of B cell hematological malignancies. These cells efficiently and specifically recognize and kill tumor cells, unrestricted by major histocompatibility complex limitations. OBJECTIVE: To elucidate the structure, developmental history, and marketed progress of chimeric antigen receptor T cells, summarize their long-term efficacy in B cell hematological malignancies treatments, and discuss associated toxicities, recurrence, and mitigation strategies. Additionally, it reviews the advancement of potential targets in B cell hematological malignancies treatments. METHODS: Searches were conducted in PubMed, CNKI, and WanFang databases using the terms “CAR-T, B cell hematological malignancies, toxic side effects, immunotherapy” in Chinese and English, focusing on articles regarding chimeric antigen receptor T cell targets in B-cell malignant tumor treatments. RESULTS AND CONCLUSION: (1) The U.S. Food and Drug Administration and National Medical Products Administration have approved 11 chimeric antigen receptor T cell products, primarily targeting CD19 and B cell maturation antigen targets in B cell hematological malignancies. (2) Long-term follow-up data indicate that chimeric antigen receptor T cell therapy provides a high remission rate and enduring responses in B cell hematological malignancies patients, albeit with recurrence issues due to antigen loss or downregulation. (3) Chimeric antigen receptor T cell therapy is associated with significant toxicities, a high recurrence rate, and drug resistance, constraining its broad application. (4) Future research should concentrate on developing new targets, combined therapies, and strategies to enhance chimeric antigen receptor T cell persistence and antitumor activity.
B cell hematological malignancies  /  chimeric antigen receptor T cells  /  immunotherapy  /  therapeutic targets  /  long-term efficacy  /  toxic side effects  /  recurrence
许凡萍, 李勤椿, 唐冬芳. 不同嵌合抗原受体T细胞相关靶点治疗B细胞血液恶性肿瘤:长期随访数据综述. 中国组织工程研究, 2026 , 30 (1) : 248 -259 . DOI: 10.12307/2025.565
. Targeting diverse chimeric antigen receptor T cell-related targets in treatment of B-cell hematological malignancies: a review of long-term follow-up data[J]. Chinese Journal of Tissue Engineering Research, 2026 , 30 (1) : 248 -259 . DOI: 10.12307/2025.565
  • 国家自然科学基金项目
  • 湖南省自然科学基金项目
  • 湖南省教育厅科学研究项目
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2026年第30卷第1期
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doi: 10.12307/2025.565
  • 首发时间:2025-05-30
  • 出版时间:2026-01-08
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  • 录用日期:2024-12-28
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国家自然科学基金项目
湖南省自然科学基金项目
湖南省教育厅科学研究项目
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    1.南科技学院,湖南省永州市 425199
    2.南科技学院,湖南省永州市 425199

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2种不同金属材料的力学参数
科
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属数
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genus
种数
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species
占总种数比例
Percentage of
total species (%)
属
Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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