• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

生产符合良好生产规范的、针对 Epstein-Barr 病毒、巨细胞病毒和腺病毒的细胞毒性 T 淋巴细胞,以预防或治疗异基因造血干细胞移植后病毒感染。

Production of good manufacturing practice-grade cytotoxic T lymphocytes specific for Epstein-Barr virus, cytomegalovirus and adenovirus to prevent or treat viral infections post-allogeneic hematopoietic stem cell transplant.

机构信息

Center for Cell and Gene Therapy, Baylor College of Medicine, Texas Children's Hospital, The Methodist Hospital, Houston, Texas 77030, USA.

出版信息

Cytotherapy. 2012 Jan;14(1):7-11. doi: 10.3109/14653249.2011.636963.

DOI:10.3109/14653249.2011.636963
PMID:22172091
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3705934/
Abstract

Infections with a range of common community viruses remain a major cause of mortality and morbidity after allogeneic hematopoietic stem cell transplantation. T cells specific for cytomegalovirus (CMV), Epstein-Barr virus (EBV) and adenoviruses can safely prevent and infections with these three most common culprits, but the manufacture of individual T cell lines for each virus would be prohibitive in terms of time and cost. We have demonstrated that T cells specific for all three viruses can be manufactured in a single culture using monocytes and EBV-transformed B lymphoblastoid cell lines (LCLs), both transduced with an adenovirus vector expressing pp65 of CMV, as antigen-presenting cells. Trivirus-specific T cell lines produced from healthy stem cell donors could prevent and treat infections with all three viruses, not only in the designated recipient, but in unrelated, partially-HLA-matched third party recipients. We now provide the details and logistics of T cell manufacture.

摘要

在异基因造血干细胞移植后,多种常见社区病毒感染仍然是导致死亡率和发病率的主要原因。针对巨细胞病毒(CMV)、EB 病毒(EBV)和腺病毒的特异性 T 细胞可以安全地预防和治疗这三种最常见的病原体,但为每种病毒制造个体 T 细胞系在时间和成本方面都是不可行的。我们已经证明,使用单核细胞和 EBV 转化的 B 淋巴母细胞系(LCL),均转导表达 CMV pp65 的腺病毒载体,作为抗原呈递细胞,可在单个培养物中制造针对这三种病毒的特异性 T 细胞。从健康的干细胞供体中产生的三病毒特异性 T 细胞系不仅可以预防和治疗指定受者的三种病毒感染,还可以预防和治疗非相关的、部分 HLA 匹配的第三方受者的三种病毒感染。现在我们提供 T 细胞制造的详细信息和物流。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30c7/3705934/24e5d7e7df1b/nihms477993f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30c7/3705934/24e5d7e7df1b/nihms477993f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30c7/3705934/24e5d7e7df1b/nihms477993f1.jpg

相似文献

1
Production of good manufacturing practice-grade cytotoxic T lymphocytes specific for Epstein-Barr virus, cytomegalovirus and adenovirus to prevent or treat viral infections post-allogeneic hematopoietic stem cell transplant.生产符合良好生产规范的、针对 Epstein-Barr 病毒、巨细胞病毒和腺病毒的细胞毒性 T 淋巴细胞,以预防或治疗异基因造血干细胞移植后病毒感染。
Cytotherapy. 2012 Jan;14(1):7-11. doi: 10.3109/14653249.2011.636963.
2
Expansion of T cells targeting multiple antigens of cytomegalovirus, Epstein-Barr virus and adenovirus to provide broad antiviral specificity after stem cell transplantation.在干细胞移植后,通过扩增针对巨细胞病毒、EB 病毒和腺病毒多种抗原的 T 细胞,提供广泛的抗病毒特异性。
Cytotherapy. 2011 Sep;13(8):976-86. doi: 10.3109/14653249.2011.575356. Epub 2011 May 4.
3
Generation of trispecific cytotoxic T cells recognizing cytomegalovirus, adenovirus, and Epstein-Barr virus: an approach for adoptive immunotherapy of multiple pathogens.识别巨细胞病毒、腺病毒和爱泼斯坦-巴尔病毒的三特异性细胞毒性T细胞的产生:一种针对多种病原体的过继性免疫疗法。
J Immunother. 2007 Jul-Aug;30(5):544-56. doi: 10.1097/CJI.0b013e3180335b7a.
4
Generation of multivirus-specific T cells to prevent/treat viral infections after allogeneic hematopoietic stem cell transplant.产生多病毒特异性T细胞以预防/治疗异基因造血干细胞移植后的病毒感染。
J Vis Exp. 2011 May 27(51):2736. doi: 10.3791/2736.
5
Antigenic competition in the generation of multi-virus-specific cell lines for immunotherapy of human cytomegalovirus, polyomavirus BK, Epstein-Barr virus and adenovirus infection in haematopoietic stem cell transplant recipients.针对造血干细胞移植受者中人类巨细胞病毒、多瘤病毒 BK、爱泼斯坦-巴尔病毒和腺病毒感染的免疫治疗,生成多病毒特异性细胞系中的抗原竞争。
Immunol Lett. 2020 Dec;228:64-69. doi: 10.1016/j.imlet.2020.09.009. Epub 2020 Oct 5.
6
Safety and clinical efficacy of rapidly-generated trivirus-directed T cells as treatment for adenovirus, EBV, and CMV infections after allogeneic hematopoietic stem cell transplant.同种异体造血干细胞移植后,三病毒靶向 T 细胞快速生成治疗腺病毒、EBV 和 CMV 感染的安全性和临床疗效。
Mol Ther. 2013 Nov;21(11):2113-21. doi: 10.1038/mt.2013.151. Epub 2013 Jun 20.
7
Simultaneous ex vivo expansion of cytomegalovirus and Epstein-Barr virus-specific cytotoxic T lymphocytes using B-lymphoblastoid cell lines expressing cytomegalovirus pp65.使用表达巨细胞病毒pp65的B淋巴母细胞系同时体外扩增巨细胞病毒和EB病毒特异性细胞毒性T淋巴细胞。
Blood. 1999 Nov 1;94(9):3242-50.
8
Simultaneous generation of multivirus-specific and regulatory T cells for adoptive immunotherapy.用于过继免疫治疗的多病毒特异性和调节性 T 细胞的同时生成。
J Immunother. 2012 Jan;35(1):42-53. doi: 10.1097/CJI.0b013e31823569e2.
9
A phase I-II trial to examine the toxicity of CMV- and EBV-specific cytotoxic T lymphocytes when used for prophylaxis against EBV and CMV disease in recipients of CD34-selected/T cell-depleted stem cell transplants.一项I-II期试验,旨在研究巨细胞病毒(CMV)和EB病毒(EBV)特异性细胞毒性T淋巴细胞用于预防CD34选择/ T细胞去除的干细胞移植受者发生EBV和CMV疾病时的毒性。
Hum Gene Ther. 2000 Jul 1;11(10):1453-63. doi: 10.1089/10430340050057521.
10
Cytomegalovirus-specific cytolytic T-cell lines and clones generated against adenovirus-pp65-infected dendritic cells.针对腺病毒 pp65 感染的树突状细胞产生的巨细胞病毒特异性细胞溶解 T 细胞系和克隆。
Biol Blood Marrow Transplant. 2001;7(5):247-56. doi: 10.1053/bbmt.2001.v7.pm11400946.

引用本文的文献

1
Facing challenges with hope: universal immune cells for hematologic malignancies.满怀希望应对挑战:用于血液系统恶性肿瘤的通用免疫细胞。
Cancer Biol Med. 2023 May 4;20(4):229-47. doi: 10.20892/j.issn.2095-3941.2022.0759.
2
Combining CD34+ stem cell selection with prophylactic pathogen and leukemia directed T-cell immunotherapy to simultaneously reduce graft versus host disease, infection, and leukemia recurrence after allogeneic stem cell transplant.将 CD34+ 干细胞选择与预防性病原体和白血病导向 T 细胞免疫疗法相结合,以在异基因干细胞移植后同时降低移植物抗宿主病、感染和白血病复发的风险。
Am J Hematol. 2023 Jan;98(1):159-165. doi: 10.1002/ajh.26594. Epub 2022 May 20.
3

本文引用的文献

1
Optimization manufacture of virus- and tumor-specific T cells.病毒和肿瘤特异性 T 细胞的优化制造。
Stem Cells Int. 2011;2011:434392. doi: 10.4061/2011/434392. Epub 2011 Sep 11.
2
Allogeneic virus-specific T cells with HLA alloreactivity do not produce GVHD in human subjects.异体 HLA 反应性病毒特异性 T 细胞在人体中不会产生移植物抗宿主病。
Blood. 2010 Nov 25;116(22):4700-2. doi: 10.1182/blood-2010-06-289991. Epub 2010 Aug 13.
3
Accelerated production of antigen-specific T cells for preclinical and clinical applications using gas-permeable rapid expansion cultureware (G-Rex).
In-situ scalable manufacturing of Epstein-Barr virus-specific T-cells using bioreactor with an expandable culture area (BECA).
采用具有可扩展培养面积的生物反应器(BECA)原位可扩展制造 Epstein-Barr 病毒特异性 T 细胞。
Sci Rep. 2022 Apr 29;12(1):7045. doi: 10.1038/s41598-022-11015-z.
4
Outcome of donor-derived TAA-T cell therapy in patients with high-risk or relapsed acute leukemia post allogeneic BMT.供体来源的TAA-T细胞疗法对异基因骨髓移植后高危或复发急性白血病患者的疗效。
Blood Adv. 2022 Apr 26;6(8):2520-2534. doi: 10.1182/bloodadvances.2021006831.
5
Variances in Antiviral Memory T-Cell Repertoire of CD45RA- and CD62L-Depleted Lymphocyte Products Reflect the Need of Individual T-Cell Selection Strategies to Reduce the Risk of GvHD while Preserving Antiviral Immunity in Adoptive T-Cell Therapy.CD45RA和CD62L缺失的淋巴细胞产物中抗病毒记忆性T细胞库的差异反映了在过继性T细胞治疗中,需要个体化的T细胞选择策略以降低移植物抗宿主病风险,同时保留抗病毒免疫力。
Transfus Med Hemother. 2021 Sep 10;49(1):30-43. doi: 10.1159/000516284. eCollection 2022 Feb.
6
Cytometric analysis of T cell phenotype using cytokine profiling for improved manufacturing of an EBV-specific T cell therapy.使用细胞因子分析进行 T 细胞表型分析,以改进 EBV 特异性 T 细胞治疗的生产。
Clin Exp Immunol. 2021 Oct;206(1):68-81. doi: 10.1111/cei.13640. Epub 2021 Jul 14.
7
Lymphocyte expansion in bioreactors: upgrading adoptive cell therapy.生物反应器中的淋巴细胞扩增:提升过继性细胞疗法
J Biol Eng. 2021 Apr 13;15(1):13. doi: 10.1186/s13036-021-00264-7.
8
Viral Infections in HSCT: Detection, Monitoring, Clinical Management, and Immunologic Implications.造血干细胞移植中的病毒感染:检测、监测、临床管理及免疫学意义
Front Immunol. 2021 Jan 20;11:569381. doi: 10.3389/fimmu.2020.569381. eCollection 2020.
9
Immunotherapy of Relapsed and Refractory Solid Tumors With Ex Vivo Expanded Multi-Tumor Associated Antigen Specific Cytotoxic T Lymphocytes: A Phase I Study.体外扩增多肿瘤相关抗原特异性细胞毒性 T 淋巴细胞治疗复发/难治性实体瘤的免疫疗法:一项 I 期研究。
J Clin Oncol. 2019 Sep 10;37(26):2349-2359. doi: 10.1200/JCO.19.00177. Epub 2019 Jul 29.
10
Adoptive T Cell Therapy Strategies for Viral Infections in Patients Receiving Haematopoietic Stem Cell Transplantation.造血干细胞移植患者病毒感染的过继细胞治疗策略。
Cells. 2019 Jan 14;8(1):47. doi: 10.3390/cells8010047.
使用透气快速扩增培养器(G-Rex)加速用于临床前和临床应用的抗原特异性 T 细胞的生产。
J Immunother. 2010 Apr;33(3):305-15. doi: 10.1097/CJI.0b013e3181c0c3cb.
4
Challenges of T cell therapies for virus-associated diseases after hematopoietic stem cell transplantation.造血干细胞移植后病毒相关性疾病的 T 细胞治疗的挑战。
Expert Opin Biol Ther. 2010 Mar;10(3):337-51. doi: 10.1517/14712590903456003.
5
Cytotoxic T lymphocyte therapy with donor T cells prevents and treats adenovirus and Epstein-Barr virus infections after haploidentical and matched unrelated stem cell transplantation.供体T细胞的细胞毒性T淋巴细胞疗法可预防和治疗单倍体相合及匹配无关供者干细胞移植后的腺病毒和EB病毒感染。
Blood. 2009 Nov 5;114(19):4283-92. doi: 10.1182/blood-2009-07-232454. Epub 2009 Aug 21.
6
Nucleofection of DCs to generate Multivirus-specific T cells for prevention or treatment of viral infections in the immunocompromised host.对树突状细胞进行核转染以产生多病毒特异性T细胞,用于预防或治疗免疫功能低下宿主中的病毒感染。
Mol Ther. 2009 Sep;17(9):1616-25. doi: 10.1038/mt.2009.140. Epub 2009 Jul 7.
7
Cytotoxic T lymphocytes as immune-therapy in haematological practice.细胞毒性T淋巴细胞在血液学实践中作为免疫疗法的应用。
Br J Haematol. 2008 Oct;143(2):169-79. doi: 10.1111/j.1365-2141.2008.07316.x. Epub 2008 Aug 7.
8
Identification of hexon-specific CD4 and CD8 T-cell epitopes for vaccine and immunotherapy.鉴定用于疫苗和免疫疗法的六邻体特异性CD4和CD8 T细胞表位。
J Virol. 2008 Jan;82(1):546-54. doi: 10.1128/JVI.01689-07. Epub 2007 Oct 17.
9
Reconstitution of adenovirus-specific cell-mediated immunity in pediatric patients after hematopoietic stem cell transplantation.造血干细胞移植后小儿患者腺病毒特异性细胞介导免疫的重建
Bone Marrow Transplant. 2007 Jun;39(11):677-86. doi: 10.1038/sj.bmt.1705645. Epub 2007 Apr 9.
10
Cellular responses to viral infection in humans: lessons from Epstein-Barr virus.人类细胞对病毒感染的反应:来自爱泼斯坦-巴尔病毒的启示。
Annu Rev Immunol. 2007;25:587-617. doi: 10.1146/annurev.immunol.25.022106.141553.