Reconstructing host-pathogen interactions: analysis of the intercellular network of macrophages and other immune cells within an aspergillosis-on-chip model.

microLife Pub Date : 2026-09-12 eCollection Date: 2026-01-01 DOI:10.1093/femsml/uqag034
Simranpreet Kaur, Anna Katharina Renner, Pauline Porschitz, Franziska Schmidt, Svenja Grau, Hannah Afolayan, Stanislaw Schmidt, Thomas Lehrnbecher-Lanzeni, Hubertus Haas, Axel A Brakhage, Marc Thilo Figge, Marie von Lilienfeld-Toal, Zoltan Cseresnyés, Susann Hartung, Susanne Jahreis
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Abstract

The human-pathogenic fungus Aspergillus fumigatus can cause life-threatening infections, particularly in immunosuppressed or neutropenic patients with hematological malignancies. The human antifungal immune response primarily relies on neutrophils with contribution from macrophages, while the roles of unconventional lymphocytes such as Natural Killer (NK) cells and mucosal-associated invariant T (MAIT) cells remain less understood. Therefore, using an advanced microfluidic "invasive aspergillosis-on-chip" (IAC) model, we investigated the coordinated antifungal response of various immune cell types in combination with macrophages within a human tissue-like 3D environment. The IAC model, initially incorporating monocyte-derived macrophages, was enhanced by perfusing either primary neutrophils, NK cells, or MAIT cells for overnight infection experiments. In this model, hyphal growth of A. fumigatus was prevented only when both macrophages and neutrophils were present. However, uncontrolled growth was detected in neutropenic patient scenarios. We observed key interactions such as conidial shuttling and metaforosis between innate immune cells, accompanied by elevated cytokine levels of e.g. IL-1β and TNFα. Importantly, NK cells applied to the vascular compartment of the IAC model significantly reduced hyphal length, confirming their antifungal activity. Similarly, MAIT cells in sufficiently high quantities reduced hyphal growth and branching, although this effect depended on the recognition of riboflavin-derived antigens, as shown by the lack of response to the A. fumigatus ΔriboB mutant strain. Together, our findings demonstrate that the advanced IAC model is a powerful tool to dissect human antifungal immunity. The interactions observed between macrophages and other immune cells highlight the importance of multi-layered defense strategies against A. fumigatus.

重建宿主-病原体相互作用:分析芯片曲霉病模型中巨噬细胞和其他免疫细胞的细胞间网络。
人类致病性真菌烟曲霉可引起危及生命的感染,特别是免疫抑制或嗜中性粒细胞减少的血液系统恶性肿瘤患者。人类抗真菌免疫反应主要依赖巨噬细胞贡献的中性粒细胞,而非常规淋巴细胞如自然杀伤细胞(NK)和粘膜相关不变T细胞(MAIT)的作用仍然知之甚少。因此,我们采用先进的微流体“侵入性芯片曲霉病”(IAC)模型,在人体组织样3D环境中研究了各种免疫细胞类型与巨噬细胞联合的协同抗真菌反应。IAC模型最初加入单核细胞来源的巨噬细胞,通过灌注原代中性粒细胞、NK细胞或MAIT细胞进行过夜感染实验来增强。在这个模型中,只有当巨噬细胞和中性粒细胞同时存在时,烟曲霉的菌丝生长才会被阻止。然而,在中性粒细胞减少患者的情况下,检测到不受控制的生长。我们观察到先天性免疫细胞之间的关键相互作用,如分生孢子穿梭和化生,伴随着IL-1β和TNFα等细胞因子水平的升高。重要的是,NK细胞应用于IAC模型的血管室显著减少菌丝长度,证实了它们的抗真菌活性。同样,足够多的MAIT细胞减少菌丝生长和分支,尽管这种作用依赖于对核黄素衍生抗原的识别,如对烟曲霉ΔriboB突变株缺乏反应所示。总之,我们的研究结果表明,先进的IAC模型是解剖人类抗真菌免疫的有力工具。巨噬细胞与其他免疫细胞之间的相互作用强调了针对烟曲霉的多层防御策略的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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