• 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

供者 CD4 T 细胞在基于阿仑单抗的 T 细胞耗竭性同种异体移植后,将混合嵌合转化为完全供者 T 细胞嵌合,并补充 CD52 阳性 T 细胞池。

Donor CD4 T cells convert mixed to full donor T-cell chimerism and replenish the CD52-positive T-cell pool after alemtuzumab-based T-cell-depleted allo-transplantation.

机构信息

Department of Medicine 3, Hematology and Oncology, Johannes Gutenberg-University, Mainz, Germany.

出版信息

Bone Marrow Transplant. 2010 Apr;45(4):668-74. doi: 10.1038/bmt.2009.212. Epub 2009 Aug 17.

DOI:10.1038/bmt.2009.212
PMID:19684624
Abstract

Donor lymphocyte infusions (DLI) are used to resolve mixed T-cell chimerism (TCC) after allo-SCT despite a substantial risk of GVHD. We analyzed the impact of prophylactic CD8-depleted (CD8(depl)) DLI in 20 recipients of anti-CD52 alemtuzumab in vivo T-cell-depleted allografts with declining donor TCC after day +60. A total of 13 patients received CD8(depl) DLI and 7 patients did not. All but one of the DLI patients converted to complete donor T-cell chimeras, whereas only one non-DLI patient converted spontaneously. DLI induced transient acute GVHD in five and extensive chronic GVHD in two patients. These data suggest the use of CD8(depl) DLI as an effective treatment for mixed TCC, particularly in patients at high risk for GVHD. We also observed that the majority of reconstituting donor-derived T cells after alemtuzumab conditioning were CD52-negative. CD8(depl) DLI significantly increased the proportion of CD52-positive CD4 T cells, whereby their beneficial effect on reconstituting the post-transplant T-cell repertoire was shown.

摘要

供者淋巴细胞输注(DLI)用于解决异基因造血干细胞移植(allo-SCT)后混合 T 细胞嵌合体(TCC),尽管存在严重的移植物抗宿主病(GVHD)风险。我们分析了在体内 T 细胞耗竭的同种异体移植后第 60 天出现供体 TCC 下降的 20 例接受抗 CD52 阿仑单抗的患者中预防性 CD8 耗竭(CD8(depl)) DLI 的影响。共有 13 例患者接受了 CD8(depl) DLI,7 例患者未接受。除了一名患者外,所有 DLI 患者均转化为完全供体 T 细胞嵌合体,而只有一名非 DLI 患者自发转化。DLI 在五名患者中诱导短暂的急性 GVHD,并在两名患者中诱导广泛的慢性 GVHD。这些数据表明,CD8(depl) DLI 可有效治疗混合 TCC,尤其是在 GVHD 风险较高的患者中。我们还观察到,在用阿仑单抗预处理后重建的供体衍生 T 细胞中,大多数为 CD52 阴性。CD8(depl) DLI 显著增加了 CD52 阳性 CD4 T 细胞的比例,表明其对重建移植后 T 细胞库具有有益作用。

相似文献

1
Donor CD4 T cells convert mixed to full donor T-cell chimerism and replenish the CD52-positive T-cell pool after alemtuzumab-based T-cell-depleted allo-transplantation.供者 CD4 T 细胞在基于阿仑单抗的 T 细胞耗竭性同种异体移植后,将混合嵌合转化为完全供者 T 细胞嵌合,并补充 CD52 阳性 T 细胞池。
Bone Marrow Transplant. 2010 Apr;45(4):668-74. doi: 10.1038/bmt.2009.212. Epub 2009 Aug 17.
2
Phase I study of high-stringency CD8 depletion of donor leukocyte infusions after allogeneic hematopoietic stem cell transplantation.异基因造血干细胞移植后供体白细胞输注的高严格性CD8细胞清除的I期研究
Transplantation. 2009 Dec 15;88(11):1312-8. doi: 10.1097/TP.0b013e3181bbf382.
3
Graft-versus-leukemia and graft-versus-host reactions after donor lymphocyte infusion are initiated by host-type antigen-presenting cells and regulated by regulatory T cells in early and long-term chimeras.供体淋巴细胞输注后的移植物抗白血病反应和移植物抗宿主反应由宿主型抗原呈递细胞启动,并在早期和长期嵌合体中由调节性T细胞调节。
Biol Blood Marrow Transplant. 2006 Apr;12(4):397-407. doi: 10.1016/j.bbmt.2005.11.519.
4
Donor lymphocyte infusion-mediated graft-versus-leukemia effects in mixed chimeras established with a nonmyeloablative conditioning regimen: extinction of graft-versus-leukemia effects after conversion to full donor chimerism.采用非清髓性预处理方案建立的混合嵌合体中供体淋巴细胞输注介导的移植物抗白血病效应:向完全供体嵌合体转化后移植物抗白血病效应的消失
Transplantation. 2003 Jul 27;76(2):297-305. doi: 10.1097/01.TP.0000072014.83469.2D.
5
Mixed chimera converted into full donor chimera with powerful graft-versus-leukemia effects but no graft-versus-host disease after non T cell-depleted HLA-mismatched peripheral blood stem cell transplantation.在非T细胞去除的HLA配型不合外周血干细胞移植后,混合嵌合体转变为完全供体嵌合体,具有强大的移植物抗白血病效应,但无移植物抗宿主病。
Bone Marrow Transplant. 2000 Sep;26(6):691-3. doi: 10.1038/sj.bmt.1702563.
6
The association of CD25 expression on donor CD8+ and CD4+ T cells with graft-versus-host disease after donor lymphocyte infusions.供体淋巴细胞输注后,供体CD8 +和CD4 + T细胞上CD25表达与移植物抗宿主病的关联。
Haematologica. 2005 Oct;90(10):1389-95.
7
Prophylactic transfer of CD8-depleted donor lymphocytes after T-cell-depleted reduced-intensity transplantation.T细胞去除的低强度移植后,进行CD8去除的供体淋巴细胞预防性转移。
Blood. 2007 Jan 1;109(1):374-82. doi: 10.1182/blood-2006-03-005769. Epub 2006 Aug 29.
8
Randomized trial of CD8+ T-cell depletion in the prevention of graft-versus-host disease associated with donor lymphocyte infusion.CD8 + T细胞清除预防供体淋巴细胞输注相关移植物抗宿主病的随机试验
Biol Blood Marrow Transplant. 2002;8(11):625-32. doi: 10.1053/bbmt.2002.v8.abbmt080625.
9
Competitive Repopulation and Allo-Immunologic Pressure Determine Chimerism Kinetics after T Cell-Depleted Allogeneic Stem Cell Transplantation and Donor Lymphocyte Infusion.竞争性再增殖和同种免疫压力决定了T细胞去除的异基因干细胞移植和供体淋巴细胞输注后的嵌合动力学。
Transplant Cell Ther. 2023 Apr;29(4):268.e1-268.e10. doi: 10.1016/j.jtct.2022.12.022. Epub 2022 Dec 30.
10
Reduced-intensity conditioning for allogeneic haematopoietic stem cell transplantation in relapsed and refractory Hodgkin lymphoma: impact of alemtuzumab and donor lymphocyte infusions on long-term outcomes.复发难治性霍奇金淋巴瘤异基因造血干细胞移植的减低剂量预处理:阿仑单抗和供体淋巴细胞输注对长期结局的影响
Br J Haematol. 2007 Oct;139(1):70-80. doi: 10.1111/j.1365-2141.2007.06759.x.

引用本文的文献

1
CD4 Donor Lymphocyte Infusion Can Cause Conversion of Chimerism Without GVHD by Inducing Immune Responses Targeting Minor Histocompatibility Antigens in HLA Class II.CD4 供者淋巴细胞输注可通过诱导针对 HLA II 类中次要组织相容性抗原的免疫反应,在无移植物抗宿主病的情况下引起嵌合状态的转换。
Front Immunol. 2018 Dec 18;9:3016. doi: 10.3389/fimmu.2018.03016. eCollection 2018.
2
Immune Reconstitution after Allogeneic Hematopoietic Stem Cell Transplantation.异基因造血干细胞移植后的免疫重建
Front Immunol. 2016 Nov 17;7:507. doi: 10.3389/fimmu.2016.00507. eCollection 2016.
3
Allo-reactive T cells for the treatment of hematological malignancies.
用于治疗血液系统恶性肿瘤的同种反应性T细胞。
Mol Oncol. 2015 Dec;9(10):1894-903. doi: 10.1016/j.molonc.2015.10.014. Epub 2015 Oct 24.
4
Phase 2 clinical trial of rapamycin-resistant donor CD4+ Th2/Th1 (T-Rapa) cells after low-intensity allogeneic hematopoietic cell transplantation.低强度异基因造血细胞移植后雷帕霉素耐药供体 CD4+ Th2/Th1(T-Rapa)细胞的 2 期临床试验。
Blood. 2013 Apr 11;121(15):2864-74. doi: 10.1182/blood-2012-08-446872. Epub 2013 Feb 20.
5
Favorable outcomes in patients with high donor-derived T cell count after in vivo T cell-depleted reduced-intensity allogeneic stem cell transplantation.在体内 T 细胞耗竭的减低强度异基因干细胞移植后,具有高供体源性 T 细胞计数的患者有良好的结局。
Biol Blood Marrow Transplant. 2012 May;18(5):794-804. doi: 10.1016/j.bbmt.2011.10.011. Epub 2011 Oct 17.
6
Recipient lymphocyte infusion in MHC-matched bone marrow chimeras induces a limited lymphohematopoietic host-versus-graft reactivity but a significant antileukemic effect mediated by CD8+ T cells and natural killer cells.受者淋巴细胞输注在 MHC 匹配的骨髓嵌合体中诱导有限的淋巴血液造血宿主抗移植物反应,但由 CD8+T 细胞和自然杀伤细胞介导的显著抗白血病效应。
Haematologica. 2011 Mar;96(3):424-31. doi: 10.3324/haematol.2010.035329. Epub 2010 Nov 25.