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一种CARD9缺陷小鼠模型重现了人类慢性中枢神经系统念珠菌病,揭示了免疫发病机制中单核细胞反应存在缺陷。

A CARD9 deficiency mouse model recapitulates human chronic CNS candidiasis identifying defective monocytic cell responses in immunopathogenesis.

作者信息

Landekic Marija, Angers Isabelle, Li Yongbiao, Guiot Marie-Christine, Déry Marc-André, Beauchamp Annie, Roussel Lucie, Boisvert Annie, Zhou Wen Bo, Gavino Christina, Luo Julia, Bernier Stéphane, Kazimerczak-Brunet Makayla, Sun Yichun, Snarr Brendan, Lionakis Michail S, Wheeler Robert T, King Irah L, Qureshi Salman T, Divangahi Maziar, Vinh Donald C

机构信息

Department of Microbiology & Immunology, McGill University, Montréal, Québec, Canada.

Meakins-Christie Laboratories, Department of Medicine, McGill University Health Centre, Montréal, Québec, Canada.

出版信息

JCI Insight. 2025 May 27;10(13). doi: 10.1172/jci.insight.176676. eCollection 2025 Jul 8.

Abstract

Human Caspase Recruitment Domain Containing Protein 9 (CARD9) deficiency predisposes to invasive fungal disease, particularly by Candida spp. CARD9 deficiency causes chronic central nervous system (CNS) candidiasis. Currently, no animal model recapitulates the chronicity of disease, precluding a better understanding of immunopathogenesis. We established a knock-in mouse homozygous for the recurring p.Y91H mutation (Y91HKI) and, in parallel to Card9-/- mice, titrated the intravenous fungal inoculum to the CARD9 genotype to develop a model of chronic invasive candidiasis. Strikingly, CARD9-deficient mice had predominantly CNS involvement, with neurological symptoms appearing late during infection and progressive brain fungal burden in the absence of fulminant sepsis, reflecting the human syndrome. Mononuclear cell aggregation at fungal lesions in the brain correlated with increased MHCII+Ly6C+ monocyte numbers at day 1 after infection in WT and Y91HKI mice, but not in Card9-/- mice. At day 4 after infection, neutrophils and additional Ly6C+ monocytes were recruited to the CARD9-deficient brain. As in humans, Y91HKI mutant mice demonstrated cerebral multinucleated giant cells and granulomata. Subtle immunologic differences between the hypomorphic (p.Y91H) and null mice were noted, perhaps explaining some of the variability seen in humans. Our work established a disease-recapitulating animal model to specifically decipher chronic CNS candidiasis due to CARD9 deficiency.

摘要

人类含半胱天冬酶招募结构域蛋白9(CARD9)缺陷易引发侵袭性真菌病,尤其是念珠菌属感染所致。CARD9缺陷会导致慢性中枢神经系统(CNS)念珠菌病。目前,尚无动物模型能够重现该病的慢性病程,这妨碍了对免疫发病机制的深入理解。我们构建了一种敲入小鼠,其纯合子携带反复出现的p.Y91H突变(Y91HKI),并与Card9-/-小鼠并行,根据CARD9基因型调整静脉注射真菌接种量,以建立慢性侵袭性念珠菌病模型。引人注目的是,CARD9缺陷小鼠主要累及中枢神经系统,在感染后期出现神经症状,且在无暴发性脓毒症的情况下脑内真菌负荷逐渐增加,反映了人类综合征。野生型和Y91HKI小鼠在感染后第1天,脑内真菌病灶处的单核细胞聚集与MHCII+Ly6C+单核细胞数量增加相关,但Card9-/-小鼠并非如此。感染后第4天,中性粒细胞和更多Ly6C+单核细胞被募集到CARD9缺陷的脑内。与人类情况一样,Y91HKI突变小鼠出现了脑内多核巨细胞和肉芽肿。我们注意到低表达(p.Y91H)小鼠和基因敲除小鼠之间存在细微的免疫差异,这或许可以解释人类中观察到的一些变异性。我们的工作建立了一种能够重现疾病的动物模型,以专门解读由CARD9缺陷引起的慢性中枢神经系统念珠菌病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a231/12288897/6db82dabc531/jciinsight-10-176676-g129.jpg

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