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本文引用的文献

1
Biology of interleukin-10.白细胞介素-10 的生物学特性。
Cytokine Growth Factor Rev. 2010 Oct;21(5):331-44. doi: 10.1016/j.cytogfr.2010.09.002. Epub 2010 Nov 5.
2
Tuberculosis is associated with a down-modulatory lung immune response that impairs Th1-type immunity.结核病与下调性肺免疫反应相关,这种反应会损害Th1型免疫。
J Immunol. 2009 Jul 1;183(1):718-31. doi: 10.4049/jimmunol.0801212. Epub 2009 Jun 17.
3
IL-10 is up-regulated in multiple cell types during viremic HIV infection and reversibly inhibits virus-specific T cells.在病毒血症期的HIV感染过程中,多种细胞类型中的白细胞介素-10(IL-10)表达上调,并可逆性抑制病毒特异性T细胞。
Blood. 2009 Jul 9;114(2):346-56. doi: 10.1182/blood-2008-12-191296. Epub 2009 Apr 13.
4
Plasmodium vivax parasites alter the balance of myeloid and plasmacytoid dendritic cells and the induction of regulatory T cells.间日疟原虫寄生虫会改变髓样和浆细胞样树突状细胞的平衡以及调节性T细胞的诱导。
Eur J Immunol. 2008 Oct;38(10):2697-705. doi: 10.1002/eji.200838186.
5
Animal models for the analysis of immune responses to leishmaniasis.用于分析利什曼病免疫反应的动物模型。
Curr Protoc Immunol. 2001 May;Chapter 19:Unit 19.2. doi: 10.1002/0471142735.im1902s28.
6
IL-10: the master regulator of immunity to infection.白细胞介素-10:感染免疫的主要调节因子。
J Immunol. 2008 May 1;180(9):5771-7. doi: 10.4049/jimmunol.180.9.5771.
7
Interleukin-10 and the pathogenesis of human visceral leishmaniasis.白细胞介素-10与人类内脏利什曼病的发病机制
Trends Immunol. 2007 Sep;28(9):378-84. doi: 10.1016/j.it.2007.07.004. Epub 2007 Aug 6.
8
Splenic accumulation of IL-10 mRNA in T cells distinct from CD4+CD25+ (Foxp3) regulatory T cells in human visceral leishmaniasis.在人类内脏利什曼病中,IL-10 mRNA在与CD4+CD25+(Foxp3)调节性T细胞不同的T细胞中脾脏蓄积。
J Exp Med. 2007 Apr 16;204(4):805-17. doi: 10.1084/jem.20061141. Epub 2007 Mar 26.
9
Innate immune responses to human malaria: heterogeneous cytokine responses to blood-stage Plasmodium falciparum correlate with parasitological and clinical outcomes.对人类疟疾的天然免疫反应:对血液期恶性疟原虫的异质性细胞因子反应与寄生虫学和临床结果相关。
J Immunol. 2006 Oct 15;177(8):5736-45. doi: 10.4049/jimmunol.177.8.5736.
10
Treatment options for visceral leishmaniasis: a systematic review of clinical studies done in India, 1980-2004.内脏利什曼病的治疗选择:对1980 - 2004年在印度开展的临床研究的系统评价
Lancet Infect Dis. 2005 Dec;5(12):763-74. doi: 10.1016/S1473-3099(05)70296-6.

白细胞介素-10 中和促进内脏利什曼病患者脾抽吸细胞中寄生虫的清除。

IL-10 neutralization promotes parasite clearance in splenic aspirate cells from patients with visceral leishmaniasis.

机构信息

Department of Medicine, Institute of Medical Sciences, Banaras Hindu University, Varanasi, India.

出版信息

J Infect Dis. 2011 Oct 1;204(7):1134-7. doi: 10.1093/infdis/jir461.

DOI:10.1093/infdis/jir461
PMID:21881130
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3164427/
Abstract

The mechanisms underlying the failure to contain the growth of Leishmania parasites in human visceral leishmaniasis (VL) are not understood. L donovani amastigotes were quantified in cultured splenic aspirate cells to assess the function of IL-10 in lesional tissue ex vivo. In 67 patients with active VL, IL-10 neutralization promoted parasite killing in 73% and complete clearance in 30%, while 18% had more parasites and 9% did not change. The splenic cells secreted increased levels of both tumor necrosis factor α (TNFα) and interferon γ (IFNγ) under IL-10-neutralizing conditions. These findings provide direct support for targeting IL-10 as an approach to therapy in human VL.

摘要

导致人体内脏利什曼病(VL)中无法控制利什曼原虫生长的机制尚不清楚。通过定量检测培养的脾抽吸细胞中的利什曼原虫无鞭毛体,评估了 IL-10 在病变组织中的功能。在 67 例活动性 VL 患者中,IL-10 中和促进了 73%的寄生虫杀伤和 30%的完全清除,而 18%的患者寄生虫增多,9%的患者寄生虫数量无变化。在 IL-10 中和条件下,脾细胞分泌的肿瘤坏死因子α(TNFα)和干扰素γ(IFNγ)水平增加。这些发现为将 IL-10 作为人类 VL 治疗方法提供了直接支持。