P118 Pentraxin-3 interacts with Aspergillus fumigatus conidia to regulate pro-inflammatory cytokine production

IF 1.4 Q4 MYCOLOGY
S. Dellière, S. Wong, C. Chauvin, J. Bayry, A. Carvalho, A. Inforzato, V. Aimanianda
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引用次数: 0

Abstract

Abstract Poster session 1, September 21, 2022, 12:30 PM - 1:30 PM Objectives Long pentraxin-3 (PTX3) is a soluble pattern-recognition receptor secreted by phagocytes and non-immune cells at sites of inflammation. It has been reported to have a nonredundant role in the immune response against Aspergillus fumigatus. Indeed, PTX3 knock-out mice show an increased susceptibility to invasive pulmonary aspergillosis (IPA) with a higher mortality rate. In humans, PTX3 genetic deficiency or single nucleotide polymorphism has also been associated with an increased risk of IPA. However, the way in which PTX3 interacts with A. fumigatus and its mechanism of action has yet to be elucidated. The aim of the study was to investigate potential A. fumigatus ligands for PTX3 and the impact of A. fumigatus opsonization by PTX3 on modulating the immune response. Methods Aspergillus fumigatus conidia, the infective morphotype, were incubated with PTX3 with or without human serum, stained with anti-PTX3 antibody, and studied by immunofluorescence. Identification of potential fungal ligands for PTX3 was performed by ELISA. Fixed conidia and germinated conidia were opsonized with different serum factors and co-incubated with human monocyte-derived macrophages (hMDM) for 24 h at 37°C. Culture supernatants were collected, and pro-/anti-inflammatory cytokines were measured by sandwich ELISA. Results PTX3 did not bind A. fumigatus conidia directly but in the presence of human serum, purified collectins [surfactant protein D (SP-D) or C1q], and complement products (C3b). Pre-opsonization of conidia with these complement proteins or SP-D stimulated proinflammatory cytokine secretion by hMDM upon interaction (Fig. 1a). In contrast, secondary opsonization of complement proteins or SP-D opsonized conidia with PTX3 significantly reduced pro-inflammatory cytokines and increased anti-inflammatory cytokine secretion from hMDM. PTX3 opsonized PFA-fixed germinating conidia significantly reduced pro-inflammatory cytokine and increased anti-inflammatory cytokines secretion from hMDM (Fig. 1b). Conclusion PTX3 is an acute phase protein expressed in response to pro-inflammatory stimuli during infection and that is increased in bronchoalveolar lavage of patients with aspergillosis. Our recent data with A. fumigatus suggest that PTX3 is an immunoregulatory protein that reduces pro-inflammatory response. Although an inflammatory response is necessary to fight against fungal pathogens, the tissue damage associated with enhanced inflammation can be deleterious and facilitate A. fumigatus infection.
P118 penttraxin -3与烟曲霉分生孢子相互作用,调节促炎细胞因子的产生
摘要:海报会议1,2022年9月21日,12:30 PM - 1:30 PM目的长pentaxin -3 (PTX3)是一种可溶性的模式识别受体,由吞噬细胞和炎症部位的非免疫细胞分泌。据报道,它在针对烟曲霉的免疫反应中具有非冗余作用。事实上,PTX3基因敲除小鼠对侵袭性肺曲霉病(IPA)的易感性增加,死亡率更高。在人类中,PTX3基因缺陷或单核苷酸多态性也与IPA风险增加有关。然而,PTX3与烟曲霉的相互作用方式及其作用机制尚不清楚。本研究的目的是研究烟曲霉PTX3的潜在配体以及PTX3对烟曲霉的调控对免疫反应的影响。方法用含或不含人血清的PTX3孵育感染型烟曲霉分生孢子,进行抗PTX3抗体染色,免疫荧光法观察。采用ELISA法鉴定PTX3潜在的真菌配体。将固定分生孢子和萌发分生孢子用不同的血清因子活化,并与人单核细胞源性巨噬细胞(hMDM)在37℃共孵育24 h。收集培养上清液,采用夹心ELISA法检测促/抗炎细胞因子。结果PTX3不直接与烟曲霉分生孢子结合,但与人血清、纯化集素[表面活性剂蛋白D (SP-D)或C1q]、补体产物(C3b)存在。分生孢子与这些补体蛋白或SP-D的预调理在相互作用后通过hMDM刺激促炎细胞因子的分泌(图1a)。相比之下,PTX3对补体蛋白或SP-D调理的分生孢子的二次调理可显著降低hMDM的促炎细胞因子和增加抗炎细胞因子的分泌。PTX3活化pfa固定的萌发分生孢子可显著降低促炎细胞因子,增加hMDM中抗炎细胞因子的分泌(图1b)。结论PTX3是一种急性期蛋白,在感染过程中对促炎刺激的反应中表达,在曲霉病患者支气管肺泡灌洗中表达增加。我们最近关于烟曲霉的数据表明,PTX3是一种免疫调节蛋白,可以减少促炎反应。虽然炎症反应是对抗真菌病原体所必需的,但与炎症增强相关的组织损伤可能是有害的,并促进烟曲霉感染。
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来源期刊
Medical mycology journal
Medical mycology journal Medicine-Infectious Diseases
CiteScore
1.80
自引率
10.00%
发文量
16
期刊介绍: The Medical Mycology Journal is published by and is the official organ of the Japanese Society for Medical Mycology. The Journal publishes original papers, reviews, and brief reports on topics related to medical and veterinary mycology.
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