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在马里感染血吸虫的儿童中,急性疟原虫感染期间 T 调节细胞反应降低。

Reduced T regulatory cell response during acute Plasmodium falciparum infection in Malian children co-infected with Schistosoma haematobium.

机构信息

Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, Maryland, United States of America.

出版信息

PLoS One. 2012;7(2):e31647. doi: 10.1371/journal.pone.0031647. Epub 2012 Feb 14.

DOI:10.1371/journal.pone.0031647
PMID:22348117
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3279404/
Abstract

BACKGROUND

Regulatory T cells (Tregs) suppress host immune responses and participate in immune homeostasis. In co-infection, secondary parasite infections may disrupt the immunologic responses induced by a pre-existing parasitic infection. We previously demonstrated that schistosomiasis-positive (SP) Malian children, aged 4-8 years, are protected against the acquisition of malaria compared to matched schistosomiasis-negative (SN) children.

METHODS AND FINDINGS

To determine if Tregs contribute to this protection, we performed immunologic and Treg depletion in vitro studies using PBMC acquired from children with and without S. haematobium infection followed longitudinally for the acquisition of malaria. Levels of Tregs were lower in children with dual infections compared to children with malaria alone (0.49 versus 1.37%, respectively, P = 0.004) but were similar months later, during a period with negligible malaria transmission. The increased levels of Tregs in SN subjects were associated with suppressed serum Th1 cytokine levels, as well as elevated parasitemia compared to co-infected counterparts.

CONCLUSIONS

These results suggest that lower levels of Tregs in helminth-infected children correlate with altered circulating cytokine and parasitologic results which may play a partial role in mediating protection against falciparum malaria.

摘要

背景

调节性 T 细胞(Tregs)抑制宿主免疫反应并参与免疫稳态。在混合感染中,二次寄生虫感染可能会破坏由先前存在的寄生虫感染引起的免疫反应。我们之前的研究表明,与匹配的无血吸虫感染的儿童相比,年龄在 4-8 岁的阳性血吸虫病(SP)马里儿童对疟疾的获得具有保护作用。

方法和发现

为了确定 Tregs 是否有助于这种保护作用,我们使用从有和没有曼氏血吸虫感染的儿童获得的 PBMC 进行了体外免疫和 Treg 耗竭研究,并对疟疾的获得进行了纵向研究。与仅患有疟疾的儿童相比,双重感染的儿童中 Tregs 的水平较低(分别为 0.49%和 1.37%,P = 0.004),但在数月后,在疟疾传播可忽略不计的时期,Tregs 的水平相似。SN 受试者中 Tregs 水平的升高与血清 Th1 细胞因子水平受到抑制以及与感染对照相比寄生虫血症升高有关。

结论

这些结果表明,感染蠕虫的儿童中 Tregs 水平较低与循环细胞因子和寄生虫学结果的改变相关,这可能在介导对恶性疟原虫疟疾的保护中发挥部分作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/710e/3279404/d4cd61651ca2/pone.0031647.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/710e/3279404/417e65801c05/pone.0031647.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/710e/3279404/d4cd61651ca2/pone.0031647.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/710e/3279404/417e65801c05/pone.0031647.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/710e/3279404/d4cd61651ca2/pone.0031647.g004.jpg

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本文引用的文献

1
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N Engl J Med. 2011 Sep 15;365(11):1004-13. doi: 10.1056/NEJMoa1008115.
2
Regulatory and activated T cells in human Schistosoma haematobium infections.人类埃及血吸虫感染中的调节性和活化 T 细胞。
PLoS One. 2011 Feb 10;6(2):e16860. doi: 10.1371/journal.pone.0016860.
3
Schistosomiasis coinfection in children influences acquired immune response against Plasmodium falciparum malaria antigens.血吸虫病合并感染会影响儿童对恶性疟原虫抗原的获得性免疫应答。
感染ANKA和(此处原文似乎不完整)的斯普拉格-道利大鼠的趋化因子、细胞因子和血液学特征——疟疾与组织内寄生线虫共感染的实验动物模型
Heliyon. 2020 Feb 25;6(2):e03475. doi: 10.1016/j.heliyon.2020.e03475. eCollection 2020 Feb.
4
The Alteration of Subtelomeric DNA Methylation in Aging-Related Diseases.衰老相关疾病中亚端粒DNA甲基化的改变。
Front Genet. 2019 Jan 9;9:697. doi: 10.3389/fgene.2018.00697. eCollection 2018.
5
The Influence of Parasite Infections on Host Immunity to Co-infection With Other Pathogens.寄生虫感染对宿主同时感染其他病原体的免疫反应的影响。
Front Immunol. 2018 Nov 8;9:2579. doi: 10.3389/fimmu.2018.02579. eCollection 2018.
6
Plasmodium and intestinal parasite perturbations of the infected host's inflammatory responses: a systematic review.疟原虫和肠道寄生虫对感染宿主炎症反应的干扰:系统评价。
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7
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Malar J. 2015 Feb 25;14:94. doi: 10.1186/s12936-015-0608-4.
PLoS One. 2010 Sep 15;5(9):e12764. doi: 10.1371/journal.pone.0012764.
4
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Clin Vaccine Immunol. 2010 Sep;17(9):1305-14. doi: 10.1128/CVI.00234-10. Epub 2010 Jul 21.
5
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