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自然杀伤细胞(NKp46)发展出一种活化/记忆样表型,并有助于针对实验性丝虫感染的固有免疫。

NKp46 natural killer cells develop an activated/memory-like phenotype and contribute to innate immunity against experimental filarial infection.

机构信息

Centre for Drugs and Diagnostics, Department of Parasitology, Liverpool School of Tropical Medicine, Liverpool, United Kingdom.

Centre for Bioscience, John Dalton Building, Faculty of Science and Engineering, Manchester Metropolitan University, Manchester, United Kingdom.

出版信息

Front Immunol. 2022 Sep 27;13:969340. doi: 10.3389/fimmu.2022.969340. eCollection 2022.

Abstract

Lymphatic filariasis and onchocerciasis are major neglected tropical diseases affecting over 90 million people worldwide with painful and profoundly disfiguring pathologies (such as lymphoedema or blindness). Type 2 inflammation is a hallmark of filarial nematode tissue infection and is implicated both in eosinophil dependent immunity and lymphatic or ocular immunopathologies. Type-2 innate lymphoid cells (ILC2) are known to play an important role in the initiation of type 2 inflammation in helminth infection. We therefore tracked comparative IL-12Rβ2 ILC1, ST2 ILC2 and NKp46 natural killer (NK) innate lymphoid cell population expansions during experimental peritoneal filarial infections using either immunocompetent or immunodeficient mice. In immunocompetent BALB/c animals, NKp46 NK cells rapidly expanded representing over 90% of the ILC population in the first week of infection, whereas, surprisingly, ST2 ILC2 failed to expand. NKp46 NK cell expansions were confirmed in RAG2 deficient mice lacking adaptive immunity. Ablation of the NKp46 NK cell compartment in RAG2 common gamma chain (gc) mice led to increased susceptibility to chronic adult infection. This data was recapitulated using an male worm peritoneal implant model. When NKp46 NK cells were depleted in RAG2 deficient mice using anti-NKp46 or asialo GM1 antibody injections over the first five weeks of infection, susceptibility to adult infection was significantly increased by 2-3 fold with concomitant impairment in eosinophil or neutrophil recruitments. Finally, we demonstrate that in RAG2 deficient mice, drug clearance of a primary adult infection followed by challenge infection leads to resistance against early larval establishment. This innate resistance is associated with bolstered NK and eosinophils whereby NKp46 NK cells express markers of memory-like/enhanced activation (increased expression of interferon gamma and Ly6C). Our data promotes a novel functional role for NKp46 NK cells in immunoprotection against experimental primary and secondary filarial infection which can proceed in the absence of adaptive immune regulation.

摘要

淋巴丝虫病和盘尾丝虫病是主要的被忽视热带病,影响着全球超过 9000 万人,导致痛苦和严重毁容的病理变化(如淋巴水肿或失明)。2 型炎症是丝虫线虫组织感染的标志,与嗜酸性粒细胞依赖的免疫和淋巴或眼部免疫病理学都有关。2 型先天淋巴样细胞(ILC2)已知在寄生虫感染中 2 型炎症的启动中发挥重要作用。因此,我们使用免疫功能正常或免疫缺陷的小鼠跟踪比较了实验性腹膜丝虫感染中 IL-12Rβ2 ILC1、ST2 ILC2 和 NKp46 自然杀伤(NK)先天淋巴样细胞群体的扩张。在免疫功能正常的 BALB/c 动物中,NKp46 NK 细胞迅速扩增,在感染的第一周内代表了 ILC 群体的 90%以上,而令人惊讶的是,ST2 ILC2 未能扩增。NKp46 NK 细胞的扩增在缺乏适应性免疫的 RAG2 缺陷小鼠中得到了证实。在 RAG2 共同γ链(gc)缺陷小鼠中,NKp46 NK 细胞区室的消融导致对慢性成年感染的易感性增加。这一数据在使用雄性蠕虫腹膜植入模型时得到了重复。当在 RAG2 缺陷小鼠中使用抗 NKp46 或抗唾液酸 GM1 抗体在感染的前 5 周内对 NKp46 NK 细胞进行耗竭时,对成年感染的易感性增加了 2-3 倍,同时伴随着嗜酸性粒细胞或中性粒细胞募集的损害。最后,我们证明在 RAG2 缺陷小鼠中,药物清除原发性成年感染,然后进行再感染,可导致对早期幼虫建立的抵抗力。这种先天抵抗与 NK 和嗜酸性粒细胞的增强有关,NKp46 NK 细胞表达记忆样/增强激活的标志物(干扰素γ和 Ly6C 的表达增加)。我们的数据为 NKp46 NK 细胞在针对实验性原发性和继发性丝虫感染的免疫保护中提供了一个新的功能作用,这种作用可以在没有适应性免疫调节的情况下进行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6a6/9551455/5cfa4e876809/fimmu-13-969340-g001.jpg

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