• 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

T-cell therapy of cytomegalovirus and human immunodeficiency virus infection.

作者信息

Riddell S R, Greenberg P D

机构信息

Fred Hutchinson Cancer Research Center and the University of Washington, Seattle 98109, USA.

出版信息

J Antimicrob Chemother. 2000 Apr;45 Suppl T3:35-43. doi: 10.1093/jac/45.suppl_4.35.

DOI:10.1093/jac/45.suppl_4.35
PMID:10855770
Abstract

Acute and persistent virus infections are limited by the development and maintenance of host T-cell responses to viral antigens. Individuals with congenital or acquired immunodeficiencies are at risk of progressive and often life-threatening infection. Recent studies have provided insight into the nature of protective T-cell responses to viruses and advances in T-cell culture technology have made it possible to evaluate the adoptive transfer of T-cell clones of defined antigen specificity and function to restore deficient responses in immunocompromised hosts. The progress of these studies in cytomegalovirus and human immunodeficiency virus infection is the subject of this review.

摘要

相似文献

1
T-cell therapy of cytomegalovirus and human immunodeficiency virus infection.
J Antimicrob Chemother. 2000 Apr;45 Suppl T3:35-43. doi: 10.1093/jac/45.suppl_4.35.
2
CD8+ cytotoxic T cell therapy of cytomegalovirus and HIV infection.巨细胞病毒和HIV感染的CD8 + 细胞毒性T细胞疗法。
Curr Opin Immunol. 1993 Aug;5(4):484-91. doi: 10.1016/0952-7915(93)90027-p.
3
Selective reconstitution of CD8+ cytotoxic T lymphocyte responses in immunodeficient bone marrow transplant recipients by the adoptive transfer of T cell clones.通过T细胞克隆的过继转移在免疫缺陷骨髓移植受者中选择性重建CD8 + 细胞毒性T淋巴细胞反应。
Bone Marrow Transplant. 1994;14 Suppl 4:S78-84.
4
Adoptive cellular therapy for early cytomegalovirus infection after allogeneic stem-cell transplantation with virus-specific T-cell lines.采用病毒特异性T细胞系对异基因干细胞移植后的早期巨细胞病毒感染进行过继性细胞治疗。
Lancet. 2003 Oct 25;362(9393):1375-7. doi: 10.1016/S0140-6736(03)14634-X.
5
Adoptive immunotherapy of human cytomegalovirus infection: potential role in protection from disease progression.
Transplant Proc. 1991 Jun;23(3 Suppl 3):97-101.
6
Cytotoxic T cells specific for cytomegalovirus: a potential therapy for immunocompromised patients.针对巨细胞病毒的细胞毒性T细胞:免疫功能低下患者的一种潜在治疗方法。
Rev Infect Dis. 1991 Nov-Dec;13 Suppl 11:S966-73. doi: 10.1093/clind/13.supplement_11.s966.
7
Principles for adoptive T cell therapy of human viral diseases.人类病毒性疾病过继性T细胞疗法的原则
Annu Rev Immunol. 1995;13:545-86. doi: 10.1146/annurev.iy.13.040195.002553.
8
Adoptive immunotherapy of HCMV infection.人巨细胞病毒感染的过继性免疫疗法。
Cytotherapy. 2007;9(8):699-711. doi: 10.1080/14653240701656046. Epub 2007 Oct 4.
9
Infusion of cytomegalovirus specific cytotoxic T lymphocytes from a sero-negative donor can facilitate resolution of infection and immune reconstitution.输注来自血清阴性供体的巨细胞病毒特异性细胞毒性T淋巴细胞可促进感染的消退和免疫重建。
Pediatr Infect Dis J. 2009 Jan;28(1):65-7. doi: 10.1097/INF.0b013e318182026f.
10
Pathogenesis of cytomegalovirus pneumonia in immunocompromised hosts.免疫功能低下宿主巨细胞病毒肺炎的发病机制。
Semin Respir Infect. 1995 Dec;10(4):199-208.

引用本文的文献

1
Bright and Early: Inhibiting Human Cytomegalovirus by Targeting Major Immediate-Early Gene Expression or Protein Function.早期研究:通过靶向主要即刻早期基因表达或蛋白功能抑制人巨细胞病毒。
Viruses. 2020 Jan 16;12(1):110. doi: 10.3390/v12010110.
2
Human cytomegalovirus vaccine development: Immune responses to look into vaccine strategy.人巨细胞病毒疫苗的开发:免疫应答与疫苗策略研究。
Hum Vaccin Immunother. 2018 Feb 1;14(2):292-303. doi: 10.1080/21645515.2017.1391433. Epub 2017 Dec 1.
3
A spread-deficient cytomegalovirus for assessment of first-target cells in vaccination.
用于评估疫苗接种中第一靶细胞的缺陷型巨细胞病毒。
J Virol. 2010 Aug;84(15):7730-42. doi: 10.1128/JVI.02696-09. Epub 2010 May 12.
4
Characterizing and optimizing immune responses to leukaemia antigens after allogeneic stem cell transplantation.异基因干细胞移植后白血病抗原免疫反应的特征分析与优化
Best Pract Res Clin Haematol. 2008 Sep;21(3):437-53. doi: 10.1016/j.beha.2008.07.004.
5
Transduction of primary lymphocytes with Epstein-Barr virus (EBV) latent membrane protein-specific T-cell receptor induces lysis of virus-infected cells: A novel strategy for the treatment of Hodgkin's disease and nasopharyngeal carcinoma.用爱泼斯坦-巴尔病毒(EBV)潜伏膜蛋白特异性T细胞受体转导原代淋巴细胞可诱导病毒感染细胞的裂解:一种治疗霍奇金病和鼻咽癌的新策略。
J Clin Immunol. 2006 Jan;26(1):22-32. doi: 10.1007/s10875-006-6532-1.
6
Generation of cytotoxic T cell responses directed to human leucocyte antigen Class I restricted epitopes from the Aspergillus f16 allergen.针对来自烟曲霉f16过敏原的人类白细胞抗原I类限制性表位产生细胞毒性T细胞应答。
Clin Exp Immunol. 2005 Apr;140(1):81-91. doi: 10.1111/j.1365-2249.2005.02738.x.
7
Long-term in vivo provision of antigen-specific T cell immunity by programming hematopoietic stem cells.通过对造血干细胞进行编程实现体内长期提供抗原特异性T细胞免疫
Proc Natl Acad Sci U S A. 2005 Mar 22;102(12):4518-23. doi: 10.1073/pnas.0500600102. Epub 2005 Mar 9.
8
Systemic priming-boosting immunization with a trivalent plasmid DNA and inactivated murine cytomegalovirus (MCMV) vaccine provides long-term protection against viral replication following systemic or mucosal MCMV challenge.用三价质粒DNA和灭活鼠巨细胞病毒(MCMV)疫苗进行全身启动-加强免疫,可在全身或黏膜MCMV攻击后提供针对病毒复制的长期保护。
J Virol. 2005 Jan;79(1):159-75. doi: 10.1128/JVI.79.1.159-175.2005.
9
DNA vaccines to attack cancer.用于对抗癌症的DNA疫苗。
Proc Natl Acad Sci U S A. 2004 Oct 5;101 Suppl 2(Suppl 2):14646-52. doi: 10.1073/pnas.0404896101. Epub 2004 Aug 3.
10
Herpesvirus infections in organ transplant recipients.器官移植受者中的疱疹病毒感染
Clin Diagn Lab Immunol. 2003 Jan;10(1):1-7. doi: 10.1128/cdli.10.1.1-7.2003.