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本文引用的文献

1
Biologic activity of irradiated, autologous, GM-CSF-secreting leukemia cell vaccines early after allogeneic stem cell transplantation.异基因干细胞移植后早期,经辐照的、自体的、分泌GM-CSF的白血病细胞疫苗的生物活性。
Proc Natl Acad Sci U S A. 2009 Sep 15;106(37):15825-30. doi: 10.1073/pnas.0908358106. Epub 2009 Aug 26.
2
Rejuvenation of the aging T cell compartment.衰老T细胞库的年轻化。
Curr Opin Immunol. 2009 Aug;21(4):454-9. doi: 10.1016/j.coi.2009.06.002. Epub 2009 Jul 14.
3
Functional unresponsiveness and replicative senescence of myeloid leukemia antigen-specific CD8+ T cells after allogeneic stem cell transplantation.异基因干细胞移植后髓系白血病抗原特异性CD8 + T细胞的功能无反应性和复制性衰老。
Clin Cancer Res. 2009 Aug 1;15(15):4944-53. doi: 10.1158/1078-0432.CCR-08-3332. Epub 2009 Jul 14.
4
Human T regulatory cell therapy: take a billion or so and call me in the morning.人类调节性T细胞疗法:先准备大约十亿个,明天早上再联系我。
Immunity. 2009 May;30(5):656-65. doi: 10.1016/j.immuni.2009.04.006.
5
Memory T cells in GVHD and GVL.移植物抗宿主病和移植物抗白血病效应中的记忆性T细胞。
Biol Blood Marrow Transplant. 2008 Jan;14(1 Suppl 1):19-20.
6
Graft-versus-leukemia effects of transplantation and donor lymphocytes.移植及供体淋巴细胞的移植物抗白血病效应
Blood. 2008 Dec 1;112(12):4371-83. doi: 10.1182/blood-2008-03-077974.
7
Adoptive cell therapy for patients with metastatic melanoma: evaluation of intensive myeloablative chemoradiation preparative regimens.转移性黑色素瘤患者的过继性细胞疗法:强化清髓性放化疗预处理方案的评估
J Clin Oncol. 2008 Nov 10;26(32):5233-9. doi: 10.1200/JCO.2008.16.5449. Epub 2008 Sep 22.
8
Donor lymphocyte infusions: the long and winding road: how should it be traveled?供体淋巴细胞输注:漫长而曲折的道路:应如何前行?
Bone Marrow Transplant. 2008 Nov;42(9):569-79. doi: 10.1038/bmt.2008.259. Epub 2008 Aug 18.
9
High response rate to donor lymphocyte infusion after allogeneic stem cell transplantation for indolent non-Hodgkin lymphoma.惰性非霍奇金淋巴瘤异基因干细胞移植后对供体淋巴细胞输注的高反应率。
Biol Blood Marrow Transplant. 2008 Jan;14(1):50-8. doi: 10.1016/j.bbmt.2007.04.013.
10
Treatment options for the management of acute leukaemia relapsing following an allogeneic transplant.异基因移植后复发的急性白血病的治疗选择。
Bone Marrow Transplant. 2008 Mar;41(5):495-503. doi: 10.1038/sj.bmt.1705888. Epub 2007 Oct 22.

异基因造血细胞治疗后的复发。

Relapse after allogeneic hematopoietic cell therapy.

机构信息

Memorial Sloan-Kettering Cancer Center, New York, New York, USA.

出版信息

Biol Blood Marrow Transplant. 2010 Jan;16(1 Suppl):S138-45. doi: 10.1016/j.bbmt.2009.10.023. Epub 2009 Oct 24.

DOI:10.1016/j.bbmt.2009.10.023
PMID:19857588
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3637945/
Abstract

Disease relapse remains a major cause of mortality following allogeneic hematopoietic cell transplantation (HCT). Over the past decade, our understanding of the biology underlying the graft-versus-tumor/leukemia (GVT) effect has increased greatly; however, several other factors affect the occurrence and outcome of relapse, including conditioning regimen, type of allograft, and the histology, status, and sensitivity to chemotherapy of the disease being treated. The mainstay of relapse treatment is donor lymphocyte infusion (DLI), but the efficacy of DLI is quite variable depending on disease histology and state. As such, there is a significant need for novel therapies and strategies for relapse following allogeneic HCT, particularly in patients for whom DLI is not an option. The National Cancer Institute is sponsoring an international workshop to address issues and research questions relative to the biology, natural history, prevention, and treatment of relapse following allogeneic HCT.

摘要

疾病复发仍然是异基因造血细胞移植(HCT)后导致死亡的主要原因。在过去的十年中,我们对移植物抗白血病/肿瘤(GVT)效应背后的生物学有了很大的了解;然而,还有其他几个因素会影响复发的发生和结果,包括预处理方案、同种异体移植物的类型以及所治疗疾病的组织学、状态和对化疗的敏感性。复发治疗的主要手段是供者淋巴细胞输注(DLI),但 DLI 的疗效因疾病组织学和状态而异。因此,对于异基因 HCT 后复发的患者,尤其是对于那些不能进行 DLI 的患者,迫切需要新的治疗方法和策略。美国国家癌症研究所正在主办一次国际研讨会,以解决与异基因 HCT 后复发的生物学、自然史、预防和治疗相关的问题和研究问题。