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本文引用的文献

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Role of dendritic cells: a step forward for the hygiene hypothesis.树突状细胞的作用:卫生假说的新进展。
Cell Mol Immunol. 2011 Jan;8(1):12-8. doi: 10.1038/cmi.2010.51. Epub 2010 Nov 8.
2
CD8α+ plasmacytoid precursor DCs induce antigen-specific regulatory T cells that enhance HSC engraftment in vivo.CD8α+ 浆细胞样前体 DC 诱导抗原特异性调节性 T 细胞,增强体内 HSC 植入。
Blood. 2011 Feb 24;117(8):2494-505. doi: 10.1182/blood-2010-06-291187. Epub 2010 Dec 29.
3
New insights into the generation of Th2 immunity and potential therapeutic targets for the treatment of asthma.深入了解 Th2 免疫的产生机制及哮喘治疗的潜在治疗靶点。
Curr Opin Allergy Clin Immunol. 2011 Feb;11(1):39-45. doi: 10.1097/ACI.0b013e328342322f.
4
Prevention of GVHD without losing GVL effect: windows of opportunity.在不丧失移植物抗肿瘤效应的情况下预防移植物抗宿主病:机会之窗。
Immunol Res. 2011 Apr;49(1-3):49-55. doi: 10.1007/s12026-010-8193-7.
5
Altered cytokine production by dendritic cells from infants with atopic dermatitis.特应性皮炎患儿树突状细胞细胞因子产生的改变。
Clin Immunol. 2010 Dec;137(3):406-14. doi: 10.1016/j.clim.2010.09.001. Epub 2010 Sep 29.
6
Functional changes of dendritic cells in hypersensivity reactions to amoxicillin.阿莫西林过敏反应中树突状细胞的功能变化。
Braz J Med Biol Res. 2010 Oct;43(10):964-8. doi: 10.1590/s0100-879x2010007500096. Epub 2010 Sep 24.
7
Influence of dendritic cells on biological activity of the homologous CIK cells and its anti-leukemia effect in vitro.树突状细胞对同源CIK细胞生物学活性的影响及其体外抗白血病作用
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2010 Aug;18(4):946-51.
8
Ultrastructural basis of enhanced antitumor cytotoxicity of cord blood-derived CTLs: a comparative analysis with peripheral blood and bone marrow.脐血来源 CTL 增强抗肿瘤细胞毒性的超微结构基础:与外周血和骨髓的比较分析。
Int J Oncol. 2010 Sep;37(3):645-53. doi: 10.3892/ijo_00000713.
9
CD4+ CD25+ regulatory T cells prevent type 1 diabetes preceded by dendritic cell-dominant invasive insulitis by affecting chemotaxis and local invasiveness of dendritic cells.CD4+ CD25+ 调节性 T 细胞通过影响树突状细胞的趋化性和局部浸润性,预防由树突状细胞主导的侵袭性胰岛炎引发的 1 型糖尿病。
J Immunol. 2010 Aug 15;185(4):2493-501. doi: 10.4049/jimmunol.1001036. Epub 2010 Jul 16.
10
Recent advances in antigen-loaded dendritic cell-based strategies for treatment of minimal residual disease in acute myeloid leukemia.基于负载抗原的树突状细胞治疗急性髓系白血病微小残留病策略的最新进展
Immunotherapy. 2010 Jan;2(1):69-83. doi: 10.2217/imt.09.85.

脐血移植中的树突状细胞:综述。

Dendritic cells in cord blood transplantation: a review.

机构信息

Clinical Hematology Department, Coimbra University Hospitals, Coimbra, Portugal.

出版信息

Stem Cells Int. 2011;2011:539896. doi: 10.4061/2011/539896. Epub 2011 Jun 16.

DOI:10.4061/2011/539896
PMID:21776281
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3137980/
Abstract

Dendritic cells (DCs) are a heterogeneous population of antigen-presenting cells derived from hematopoietic progenitors that bridge the transition between the innate and adaptive immune responses, while maintaining self-tolerance and Th1/Th2 homeostasis, by priming other cells in either an immunogenic or tolerogenic direction. Through their role in both innate and adaptive immunity, DCs play a major part in transplant engraftment and rejection and in graft-versus-host disease (GvHD). Preferentially tolerogenic or immunogenic DC subtypes offer targets for immunotherapy, to optimize transplant success rates and prolong disease-free and overall survival. Cord blood DCs are immature and preferentially tolerogenic, due to maternal-fetal tolerance, leading to better graft acceptance and immune reconstitution and explaining the lower incidence and severity of GvHD in CB transplantation, despite donor-host mismatching. Manipulation of DC maturation and cell loading with tumor-antigens can direct antitumor immunity and target minimal residual disease, as demonstrated for acute myeloid leukemia, optimizing the graft-versus-leukemia effect.

摘要

树突状细胞(DCs)是一种异质性的抗原呈递细胞群体,来源于造血祖细胞,在固有免疫和适应性免疫反应之间架起桥梁,同时通过向其他细胞呈递免疫原性或耐受性方向来维持自身耐受和 Th1/Th2 平衡。通过其在固有免疫和适应性免疫中的作用,DCs 在移植植入和排斥以及移植物抗宿主病(GvHD)中起着重要作用。优先具有耐受性或免疫原性的 DC 亚型为免疫治疗提供了目标,以优化移植成功率并延长无病和总生存时间。由于母婴耐受,脐血 DC 不成熟且优先具有耐受性,导致更好的移植物接受和免疫重建,这解释了 CB 移植中尽管存在供体-宿主不匹配,但 GvHD 的发生率和严重程度较低。通过操纵 DC 成熟和用肿瘤抗原加载细胞,可以引导抗肿瘤免疫并靶向微小残留疾病,如急性髓系白血病所示,从而优化移植物抗白血病效应。