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1
Necrosis and apoptosis in Trichinella spiralis-mediated tumour reduction.旋毛虫介导的肿瘤缩小中的坏死与凋亡。
Cent Eur J Immunol. 2015;40(1):42-53. doi: 10.5114/ceji.2015.50832. Epub 2015 Apr 22.
2
Immunomodulatory effects of Trichinella spiralis-derived excretory-secretory antigens.旋毛虫来源的排泄分泌抗原的免疫调节作用
Immunol Res. 2015 Mar;61(3):312-25. doi: 10.1007/s12026-015-8626-4.
3
Parasitic nematode-induced CD4+Foxp3+T cells can ameliorate allergic airway inflammation.寄生线虫诱导的CD4+Foxp3+T细胞可改善过敏性气道炎症。
PLoS Negl Trop Dis. 2014 Dec 18;8(12):e3410. doi: 10.1371/journal.pntd.0003410. eCollection 2014 Dec.
4
Glycans expressed on Trichinella spiralis excretory-secretory antigens are important for anti-inflamatory immune response polarization.旋毛虫排泄分泌抗原上表达的聚糖对于抗炎症免疫反应极化很重要。
Comp Immunol Microbiol Infect Dis. 2014 Dec;37(5-6):355-67. doi: 10.1016/j.cimid.2014.10.004. Epub 2014 Oct 28.
5
Effects of helminth co-infections on atopy, asthma and cytokine production in children living in a poor urban area in Latin America.蠕虫共感染对拉丁美洲贫困城市地区儿童特应性、哮喘及细胞因子产生的影响。
BMC Res Notes. 2014 Nov 19;7:817. doi: 10.1186/1756-0500-7-817.
6
Coinfection. Virus-helminth coinfection reveals a microbiota-independent mechanism of immunomodulation.合并感染。病毒-寄生虫合并感染揭示了一种独立于微生物群的免疫调节机制。
Science. 2014 Aug 1;345(6196):578-82. doi: 10.1126/science.1256942. Epub 2014 Jul 17.
7
Immunology. How helminths go viral.免疫学。寄生虫如何感染病毒。
Science. 2014 Aug 1;345(6196):517-8. doi: 10.1126/science.1258443. Epub 2014 Jul 31.
8
Reduced asthma morbidity in endemic areas for helminth infections: a longitudinal ecological study in Brazil.寄生虫感染流行地区哮喘发病率降低:巴西的一项纵向生态学研究
J Asthma. 2014 Dec;51(10):1022-7. doi: 10.3109/02770903.2014.936454. Epub 2014 Jun 30.
9
The low global burden of trichinellosis: evidence and implications.旋毛虫病的全球低负担:证据与启示
Int J Parasitol. 2015 Feb;45(2-3):95-9. doi: 10.1016/j.ijpara.2014.05.006. Epub 2014 Jun 19.
10
Parasitic worms and allergies in childhood: insights from population studies 2008-2013.儿童时期的寄生虫和过敏:2008-2013 年的人口研究见解。
Pediatr Allergy Immunol. 2014 May;25(3):208-17. doi: 10.1111/pai.12174. Epub 2013 Dec 10.

旋毛虫肌幼虫的分泌产物与免疫调节:对自身免疫性疾病、过敏和恶性肿瘤的影响。

Secretory Products of Trichinella spiralis Muscle Larvae and Immunomodulation: Implication for Autoimmune Diseases, Allergies, and Malignancies.

机构信息

Institute for the Application of Nuclear Energy (INEP), University of Belgrade, Banatska 31b, 11080 Belgrade, Serbia.

Centre for Infectious Disease Control Netherlands, National Institute for Public Health and the Environment (RIVM), P.O. Box 1, 3720 BA Bilthoven, Netherlands.

出版信息

J Immunol Res. 2015;2015:523875. doi: 10.1155/2015/523875. Epub 2015 May 31.

DOI:10.1155/2015/523875
PMID:26114122
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4465845/
Abstract

Trichinella spiralis has the unique ability to make itself "at home" by creating and hiding in a new type of cell in the host body that is the nurse cell. From this immunologically privileged place, the parasite orchestrates a long-lasting molecular cross talk with the host through muscle larvae excretory-secretory products (ES L1). Those products can successfully modulate parasite-specific immune responses as well as responses to unrelated antigens (either self or nonself in origin), providing an anti-inflammatory milieu and maintaining homeostasis. It is clear, based on the findings from animal model studies, that T. spiralis and its products induce an immunomodulatory network (which encompasses Th2- and Treg-type responses) that may allow the host to deal with various hyperimmune-associated disorders as well as tumor growth, although the latter still remains unclear. This review focuses on studies of the molecules released by T. spiralis, their interaction with pattern recognition receptors on antigen presenting cells, and subsequently provoked responses. This paper also addresses the immunomodulatory properties of ES L1 molecules and how the induced immunomodulation influences the course of different experimental inflammatory and malignant diseases.

摘要

旋毛虫具有独特的能力,通过在宿主体内创建和隐藏一种新型细胞——滋养细胞,使自己“安家落户”。寄生虫从这个免疫特权位置,通过肌肉幼虫排泄-分泌产物(ES L1)与宿主进行持久的分子对话。这些产物可以成功调节寄生虫特异性免疫反应以及对无关抗原(无论是自身还是非自身来源)的反应,提供抗炎环境并维持体内平衡。根据动物模型研究的结果,很明显,旋毛虫及其产物诱导了一种免疫调节网络(包括 Th2 和 Treg 型反应),这可能使宿主能够应对各种与高免疫相关的疾病以及肿瘤生长,尽管后者仍不清楚。这篇综述重点关注旋毛虫释放的分子及其与抗原呈递细胞上模式识别受体的相互作用,以及随后引发的反应。本文还讨论了 ES L1 分子的免疫调节特性以及诱导的免疫调节如何影响不同实验性炎症和恶性疾病的进程。