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本文引用的文献

1
Eosinophils mediate SIgA production triggered by TLR2 and TLR4 to control Ascaris suum infection in mice.嗜酸性粒细胞通过 TLR2 和 TLR4 介导的 SIgA 产生来控制小鼠感染猪蛔虫。
PLoS Pathog. 2021 Nov 16;17(11):e1010067. doi: 10.1371/journal.ppat.1010067. eCollection 2021 Nov.
2
Contribution of sex‑based immunological differences to the enhanced immune response in female mice following vaccination with hepatitis B vaccine.乙型肝炎疫苗接种后女性小鼠增强免疫反应中基于性别的免疫差异的贡献。
Mol Med Rep. 2019 Jul;20(1):103-110. doi: 10.3892/mmr.2019.10231. Epub 2019 May 10.
3
Biological sex affects vaccine efficacy and protection against influenza in mice.生物性别会影响流感疫苗在小鼠中的效果和保护作用。
Proc Natl Acad Sci U S A. 2018 Dec 4;115(49):12477-12482. doi: 10.1073/pnas.1805268115. Epub 2018 Nov 19.
4
Sexual dimorphism in immunity across animals: a meta-analysis.动物免疫中的性别二态性:荟萃分析。
Ecol Lett. 2018 Dec;21(12):1885-1894. doi: 10.1111/ele.13164. Epub 2018 Oct 4.
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Complex interactions in soil-transmitted helminth co-infections from a cross-sectional study in Sri Lanka.土壤传播性蠕虫混合感染的复杂相互作用:来自斯里兰卡的一项横断面研究。
Trans R Soc Trop Med Hyg. 2018 Aug 1;112(8):397-404. doi: 10.1093/trstmh/try068.
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Antibody trapping: A novel mechanism of parasite immune evasion by the trematode Echinostoma caproni.抗体捕获:卡氏棘口吸虫逃避寄生虫免疫的一种新机制。
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Sex differences in immune responses.性别差异与免疫反应。
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遗传背景影响黏膜分泌型免疫球蛋白 A 水平、寄生虫负担、肺部炎症和小鼠对感染的易感性。

Genetic Background Affects the Mucosal Secretory IgA Levels, Parasite Burden, Lung Inflammation, and Mouse Susceptibility to Infection.

机构信息

Department of Parasitology, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.

Department of Morphology, Center of Biology and Health Sciences, Universidade Federal de Sergipe, São Cristóvão, Sergipe, Brazil.

出版信息

Infect Immun. 2022 Feb 17;90(2):e0059521. doi: 10.1128/IAI.00595-21. Epub 2021 Nov 22.

DOI:10.1128/IAI.00595-21
PMID:34807734
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8852741/
Abstract

Ascariasis is a neglected tropical disease that is widespread in the world and has important socioeconomic impacts. The presence of various stages of worm development in the pulmonary and intestinal mucosae induces a humoral and cellular immune response. However, although there is much evidence of the protective role of mucosal immunity against various pathogens, including helminths, there is still a gap in the knowledge about the immune response and the mechanisms of action that are involved in protection against diseases, especially in the initial phase of ascariasis. Thus, the aim of this study was to evaluate the kinetic aspects of the immune parasitological parameters in intestinal and pulmonary mucosae in male mice with early ascariasis. Therefore, two mouse strains that showed different susceptibilities to ascariasis (BALB/c and C57BL/6J) when experimentally infected with 2,500 infective eggs of Ascaris suum from time point 0 were examined: the immune parasitological parameters were evaluated each 2 days after infection over a period of 12 days. The results were suggestive of a synergetic action of intestinal and pulmonary secretory IgA (S-IgA) contributing to protection against early ascariasis by reducing the amount of migrating larvae as well as the influx of leukocytes in the lung and the consequent impairment of pulmonary capacity.

摘要

蛔虫病是一种被忽视的热带病,在世界范围内广泛存在,对社会经济有重要影响。各种阶段的虫体在肺和肠道黏膜中发育,会引起体液和细胞免疫反应。然而,尽管有大量证据表明黏膜免疫对包括蠕虫在内的各种病原体具有保护作用,但对于免疫反应以及与疾病保护相关的作用机制仍存在知识空白,特别是在蛔虫病的初始阶段。因此,本研究旨在评估早期蛔虫病雄性小鼠肠道和肺部黏膜中寄生虫免疫参数的动态变化。为此,我们选择了两种在实验感染 2500 个猪蛔虫感染性虫卵时对蛔虫病易感性不同的小鼠品系(BALB/c 和 C57BL/6J):从感染后 0 天开始,每隔 2 天评估一次感染后 12 天内的寄生虫免疫参数。结果表明,肠道和肺部分泌型免疫球蛋白 A(S-IgA)的协同作用有助于预防早期蛔虫病,减少迁移幼虫的数量,并减少白细胞在肺部的浸润,从而降低肺部容量的损害。