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植酸损害多房棘球绦虫感染中的巨噬细胞炎症反应。

Phytic acid impairs macrophage inflammatory response in Echinococcus multilocularis infection.

作者信息

Salzmann Manuel, Resch Ulrike, Boccuni Laura, Schneider Carina, Pichler Elena T, Brekalo Mira, Uhrin Pavel, Kronenberg Philipp A, Wassermann Marion, Romig Thomas, Wojta Johann, Hohensinner Philipp J

机构信息

Department of Internal Medicine II/Cardiology, Medical University of Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.

Institute of Vascular Biology and Thrombosis Research, Centre of Physiology and Pharmacology, Medical University of Vienna, Schwarzspanierstraße 17, 1090, Vienna, Austria.

出版信息

Commun Biol. 2025 Jun 5;8(1):871. doi: 10.1038/s42003-025-08283-6.

DOI:10.1038/s42003-025-08283-6
PMID:40473753
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12141607/
Abstract

The helminth Echinococcus multilocularis relies on immune evasion strategies to persist within its host. The laminated layer (LL) surrounding the parasite provides physical protection while modulating host immune responses. E. multilocularis' immunomodulatory mechanisms are poorly understood and we explored the role of phytic acid, a known component of E. granulosus sensu lato. We show that phytic acid is also present in E. multilocularis-infected tissue and impairs macrophage inflammation. In vivo, inflammatory macrophages accumulate near the metacestode, yet do not express IL-6, indicating anti-inflammatory modulation. In vitro, phytic acid reduces pro-inflammatory cytokines such as IL-6 and IL-1β by lowering intracellular calcium levels in macrophages. This calcium-chelating effect is mirrored by the anti-inflammatory properties of an E. multilocularis metacestode extract, revealing a protein-independent immune modulation strategy. These findings suggest that phytic acid plays a crucial role in E. multilocularis' ability to suppress host immune responses and supports the parasite's long-term survival.

摘要

多房棘球绦虫这种蠕虫依靠免疫逃避策略在其宿主体内生存。寄生虫周围的分层层(LL)在调节宿主免疫反应的同时提供物理保护。多房棘球绦虫的免疫调节机制尚不清楚,我们探究了植酸(细粒棘球绦虫复合体的一种已知成分)的作用。我们发现,在多房棘球绦虫感染的组织中也存在植酸,它会损害巨噬细胞炎症反应。在体内,炎性巨噬细胞在原头蚴附近积聚,但不表达白细胞介素-6(IL-6),表明存在抗炎调节。在体外,植酸通过降低巨噬细胞内的钙水平来减少白细胞介素-6和白细胞介素-1β等促炎细胞因子。多房棘球绦虫原头蚴提取物的抗炎特性也体现了这种钙螯合效应,揭示了一种不依赖蛋白质的免疫调节策略。这些发现表明,植酸在多房棘球绦虫抑制宿主免疫反应的能力中起着关键作用,并支持寄生虫的长期生存。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b35b/12141607/7095c7667e5e/42003_2025_8283_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b35b/12141607/300681b0e3f6/42003_2025_8283_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b35b/12141607/57f0ec0d045f/42003_2025_8283_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b35b/12141607/e2ec19c8b6e2/42003_2025_8283_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b35b/12141607/ecc1f24bc34d/42003_2025_8283_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b35b/12141607/22e57d09ea6a/42003_2025_8283_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b35b/12141607/7095c7667e5e/42003_2025_8283_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b35b/12141607/300681b0e3f6/42003_2025_8283_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b35b/12141607/57f0ec0d045f/42003_2025_8283_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b35b/12141607/e2ec19c8b6e2/42003_2025_8283_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b35b/12141607/ecc1f24bc34d/42003_2025_8283_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b35b/12141607/22e57d09ea6a/42003_2025_8283_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b35b/12141607/7095c7667e5e/42003_2025_8283_Fig6_HTML.jpg

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本文引用的文献

1
The Acute Inflammatory Potential of Particles From the Echinococcus granulosus Laminated Layer Is Moderated by Its Calcium Inositol Hexakisphosphate Component.包虫病(棘球蚴病)分层囊壁颗粒的急性炎症潜能受其六磷酸肌醇钙成分的调节。
Parasite Immunol. 2024 May;46(5):e13040. doi: 10.1111/pim.13040.
2
Modulatory actions of antigen B on macrophage inflammatory activation.抗原 B 对巨噬细胞炎症激活的调节作用。
Front Cell Infect Microbiol. 2024 Mar 18;14:1362765. doi: 10.3389/fcimb.2024.1362765. eCollection 2024.
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Characterization of the immunosuppressive environment induced by larval during chronic experimental infection.
描述幼虫诱导的慢性实验感染中的免疫抑制环境。
Infect Immun. 2024 Feb 13;92(2):e0027623. doi: 10.1128/iai.00276-23. Epub 2024 Jan 4.
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Monoclonal antibody-based localization of major diagnostic antigens in metacestode tissue, excretory/secretory products, and extracellular vesicles of species.单克隆抗体定位 种的中绦期组织、排泄/分泌产物和细胞外囊泡中的主要诊断抗原。
Front Cell Infect Microbiol. 2023 Mar 16;13:1162530. doi: 10.3389/fcimb.2023.1162530. eCollection 2023.
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Immunology of a unique biological structure: the Echinococcus laminated layer.独特生物结构的免疫学:细粒棘球蚴层状囊壁。
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Alveolar echinococcosis in immunocompromised hosts.免疫功能低下宿主中的肺泡型棘球蚴病。
Clin Microbiol Infect. 2023 May;29(5):593-599. doi: 10.1016/j.cmi.2022.12.010. Epub 2022 Dec 15.
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Stress signaling boosts interferon-induced gene transcription in macrophages.应激信号增强巨噬细胞中干扰素诱导的基因转录。
Sci Signal. 2022 Dec 13;15(764):eabq5389. doi: 10.1126/scisignal.abq5389.
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Phytic Acid Maintains the Integrity of the Blood-Milk Barrier by Regulating Inflammatory Response and Intestinal Flora Structure.植酸通过调节炎症反应和肠道菌群结构来维持血乳屏障的完整性。
J Agric Food Chem. 2022 Jan 12;70(1):381-391. doi: 10.1021/acs.jafc.1c06270. Epub 2021 Dec 30.
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Inositol hexaphosphate modulates the behavior of macrophages through alteration of gene expression involved in pathways of pro- and anti-inflammatory responses, and resolution of inflammation pathways.肌醇六磷酸通过改变参与促炎和抗炎反应途径以及炎症消退途径的基因表达来调节巨噬细胞的行为。
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