• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

法国弓形虫病患者的动态免疫谱。

Dynamic Immune Profile in French Toxoplasmosis Patients.

机构信息

Institut de Parasitologie et de Pathologie Tropicale, UR7292 Dynamique des Interactions Hôte Pathogène, Fédération de Médecine Translationnelle, Université de Strasbourg, Strasbourg, France.

Laboratoire de Parasitologie et Mycologie Médicale, Les Hôpitaux Universitaires de Strasbourg, Strasbourg, France.

出版信息

J Infect Dis. 2022 Nov 11;226(10):1834-1841. doi: 10.1093/infdis/jiac305.

DOI:10.1093/infdis/jiac305
PMID:35978487
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9650498/
Abstract

BACKGROUND

Toxoplasma gondii infection is usually benign in Europe due to the strong predominance of type II strains. Few studies have been conducted to examine the immunological course of infection in humans and have yielded conflicting results, maybe influenced by heterogeneous parasite strains.

METHODS

We measured 23 immune mediators in 39, 40, and 29 sera of French noninfected, acutely infected, and chronically infected immunocompetent pregnant women, respectively.

RESULTS

Four different cytokine patterns were identified regarding their dynamics through infection phases. For 11 of the cytokines (IFN-β, IFN-γ, IL-4, IL5, IL-6, IL-10, IL-12, IL-15, CXCL9, CCL2, and CSF2) the serum levels were significantly elevated during acute infection. The inflammatory mediators IL-1β, IL-17A, IL-18, TNF-α, and CSF3 remained unchanged during acute infection, while they were significantly lower in chronically infected compared to noninfected patients. As for the anti-inflammatory cytokines TGF-β and CCL5, their levels remained significantly elevated during chronic infection. We also observed a significant negative correlation of several cytokine concentrations with IgG levels, indicating a rapid decline of serum concentrations during the acute phase.

CONCLUSIONS

These results indicate an anti-inflammatory pattern in chronically infected patients in a type II dominated setting and demonstrate the highly dynamic immune situation during acute infection.

摘要

背景

由于 II 型菌株的强烈优势,欧洲的弓形虫感染通常是良性的。很少有研究检查人类感染的免疫过程,并且产生了相互矛盾的结果,这可能受到寄生虫菌株的异质性的影响。

方法

我们分别测量了 39、40 和 29 名法国未感染、急性感染和慢性感染免疫功能正常孕妇的血清中的 23 种免疫介质。

结果

根据感染阶段的动态,确定了四种不同的细胞因子模式。对于 11 种细胞因子(IFN-β、IFN-γ、IL-4、IL5、IL-6、IL-10、IL-12、IL-15、CXCL9、CCL2 和 CSF2),血清水平在急性感染期间显著升高。炎症介质 IL-1β、IL-17A、IL-18、TNF-α 和 CSF3 在急性感染期间保持不变,而在慢性感染与未感染患者相比则明显降低。对于抗炎细胞因子 TGF-β和 CCL5,其水平在慢性感染期间仍显著升高。我们还观察到几种细胞因子浓度与 IgG 水平呈显著负相关,表明血清浓度在急性阶段迅速下降。

结论

这些结果表明在 II 型主导的环境中慢性感染患者中存在抗炎模式,并证明了急性感染期间高度动态的免疫情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a46/9650498/fab6fa48854a/jiac305f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a46/9650498/1f781b0d1317/jiac305f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a46/9650498/fab6fa48854a/jiac305f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a46/9650498/1f781b0d1317/jiac305f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a46/9650498/fab6fa48854a/jiac305f2.jpg

相似文献

1
Dynamic Immune Profile in French Toxoplasmosis Patients.法国弓形虫病患者的动态免疫谱。
J Infect Dis. 2022 Nov 11;226(10):1834-1841. doi: 10.1093/infdis/jiac305.
2
Analysis of cytokines IFN-γ, TNF-α, TGF-β and nitric oxide in amniotic fluid and serum of pregnant women with toxoplasmosis in southern Brazil.巴西南部弓形虫病孕妇羊水中细胞因子 IFN-γ、TNF-α、TGF-β 和一氧化氮的分析。
Cytokine. 2018 Jun;106:35-39. doi: 10.1016/j.cyto.2018.02.023. Epub 2018 Mar 14.
3
Increased levels of IL-17A in serum and amniotic fluid of pregnant women with acute toxoplasmosis.孕妇急性弓形虫病时血清和羊水白介素-17A 水平升高。
Acta Trop. 2021 Oct;222:106019. doi: 10.1016/j.actatropica.2021.106019. Epub 2021 Jun 19.
4
[Rudolf-Virchow Prize 1998. Award lecture. Toxoplasmosis: a model infection for studying systemic and intracerebral immune reactions].[1998年鲁道夫·魏尔啸奖。获奖演讲。弓形虫病:用于研究全身和脑内免疫反应的模型感染]
Verh Dtsch Ges Pathol. 1998;82:9-22.
5
Cytokines and chemokines production by mononuclear cells from parturient women after stimulation with live Toxoplasma gondii.产褥期妇女单核细胞在活弓形虫刺激下产生细胞因子和趋化因子。
Placenta. 2012 Sep;33(9):682-7. doi: 10.1016/j.placenta.2012.05.013. Epub 2012 Jun 27.
6
Immunoregulation by Toxoplasma gondii infection prevents allergic immune responses in mice.弓形虫感染介导的免疫调节可预防小鼠的过敏性免疫反应。
Int J Parasitol. 2009 Mar;39(4):465-72. doi: 10.1016/j.ijpara.2008.09.003. Epub 2008 Oct 2.
7
Genetic modifications of cytokine genes and Toxoplasma gondii infections in pregnant women.孕妇细胞因子基因的遗传修饰和弓形虫感染。
Microb Pathog. 2018 Aug;121:283-292. doi: 10.1016/j.micpath.2018.05.048. Epub 2018 May 31.
8
Production of gamma interferon by natural killer cells from Toxoplasma gondii-infected SCID mice: regulation by interleukin-10, interleukin-12, and tumor necrosis factor alpha.来自弓形虫感染的严重联合免疫缺陷(SCID)小鼠的自然杀伤细胞产生γ干扰素:受白细胞介素-10、白细胞介素-12和肿瘤坏死因子α的调节
Infect Immun. 1994 Jul;62(7):2818-24. doi: 10.1128/iai.62.7.2818-2824.1994.
9
Cytokine profile in murine toxoplasmosis.鼠弓形虫病的细胞因子谱。
Asian Pac J Trop Med. 2011 Jan;4(1):16-9. doi: 10.1016/S1995-7645(11)60024-2. Epub 2011 Jan 15.
10
In the absence of endogenous IL-10, mice acutely infected with Toxoplasma gondii succumb to a lethal immune response dependent on CD4+ T cells and accompanied by overproduction of IL-12, IFN-gamma and TNF-alpha.在缺乏内源性白细胞介素-10的情况下,急性感染刚地弓形虫的小鼠会死于一种依赖于CD4 + T细胞的致死性免疫反应,并伴有白细胞介素-12、γ干扰素和肿瘤坏死因子-α的过量产生。
J Immunol. 1996 Jul 15;157(2):798-805.

引用本文的文献

1
Interleukin Activity in Miscarried Women with Toxoplasmosis and Anti Thyroid Peroxidase (Anti-TPO).弓形虫病和抗甲状腺过氧化物酶(抗TPO)流产女性的白细胞介素活性
Iran J Parasitol. 2025 Apr-Jun;20(2):307-315. doi: 10.18502/ijpa.v20i2.19050.
2
Cytotoxic Signature and IFN-γ Production Dominate CD4 T-Cell Response During Human Toxoplasmosis.细胞毒性特征和γ干扰素产生在人类弓形虫病期间主导CD4 T细胞反应。
Immunology. 2025 Jun;175(2):151-164. doi: 10.1111/imm.13912. Epub 2025 Mar 4.

本文引用的文献

1
Gene expression of two innate cytokines in a miscarriage toxoplasmosis woman.流产型弓形虫病女性体内两种固有细胞因子的基因表达
Ann Parasitol. 2021;67(2):281-286. doi: 10.17420/ap6702.340.
2
Local and systemic gene expression levels of IL-10, IL-17 and TGF-β in active ocular toxoplasmosis in humans.人类活动期眼弓形虫病局部和全身的 IL-10、IL-17 和 TGF-β 的基因表达水平。
Cytokine. 2021 Oct;146:155643. doi: 10.1016/j.cyto.2021.155643. Epub 2021 Jul 28.
3
Putative biomarkers for early diagnosis and prognosis of congenital ocular toxoplasmosis.
先天性眼弓形虫病早期诊断和预后的推测性生物标志物。
Sci Rep. 2020 Oct 7;10(1):16757. doi: 10.1038/s41598-020-73265-z.
4
Serotyping, host genes and cytokines response in human ocular toxoplasmosis.人类眼弓形虫病的血清型、宿主基因与细胞因子反应。
Microb Pathog. 2020 Nov;148:104465. doi: 10.1016/j.micpath.2020.104465. Epub 2020 Aug 27.
5
Pathogenesis of ocular toxoplasmosis.眼弓形体病的发病机制。
Prog Retin Eye Res. 2021 Mar;81:100882. doi: 10.1016/j.preteyeres.2020.100882. Epub 2020 Jul 24.
6
Circulating inflammatory mediators as biomarkers of ocular toxoplasmosis in acute and in chronic infection.循环炎症介质作为急性和慢性感染性眼弓形虫病的生物标志物。
J Leukoc Biol. 2020 Oct;108(4):1253-1264. doi: 10.1002/JLB.4MA0420-702R. Epub 2020 May 18.
7
Human immunity to Toxoplasma gondii.人类对刚地弓形虫的免疫力。
PLoS Pathog. 2019 Dec 12;15(12):e1008097. doi: 10.1371/journal.ppat.1008097. eCollection 2019 Dec.
8
Association of TREM-1, IL-1β, IL-33/ST2, and TLR Expressions With the Pathogenesis of Ocular Toxoplasmosis in Mouse Models on Different Genetic Backgrounds.不同遗传背景小鼠模型中TREM-1、IL-1β、IL-33/ST2和TLR表达与眼弓形虫病发病机制的关联
Front Microbiol. 2019 Oct 9;10:2264. doi: 10.3389/fmicb.2019.02264. eCollection 2019.
9
HIV-Related Cerebral Toxoplasmosis Revisited: Current Concepts and Controversies of an Old Disease.再探与HIV相关的脑弓形虫病:一种古老疾病的当前概念与争议
J Int Assoc Provid AIDS Care. 2019 Jan-Dec;18:2325958219867315. doi: 10.1177/2325958219867315.
10
effector TgIST blocks type I interferon signaling to promote infection.效应器 TgIST 阻断 I 型干扰素信号转导以促进感染。
Proc Natl Acad Sci U S A. 2019 Aug 27;116(35):17480-17491. doi: 10.1073/pnas.1904637116. Epub 2019 Aug 14.