k18-hACE2小鼠与SARS-CoV-2脑感染相关的原发性小脑膜组织细胞淋巴细胞增生性疾病1例报告

IF 2.9 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Néstor Porras, Lidia Sánchez-Morales, Marta Pérez-Sancho, Lucas Domínguez, Antonio Rodríguez-Bertos
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引用次数: 0

摘要

背景:中枢神经系统的组织细胞增殖性疾病是罕见的,它们与病毒感染的潜在联系在很大程度上仍未被探索。该病例具有相关性,因为它表明SARS-CoV-2神经侵袭与肿瘤发展之间存在潜在的相互作用,为病毒感染如何影响肿瘤发生提供了见解。病例介绍:一只4.5个月大的雄性k18-hACE-2小鼠,是SARS-CoV-2实验研究的一部分,在脑膜轻脑膜区显示由肿瘤圆形细胞组成的小肿块。这一过程与典型的急性炎症和神经退行性病变有关。组织病理学显示肿瘤由淋巴母细胞和大量组织细胞样细胞混合组成。免疫组化显示Iba-1在组织细胞中高表达,但PAX5、CD3和IRF-4标记阴性。由于PAX-5在维持b细胞功能中的关键作用,其减少或失活可能有利于这种身份丧失和向巨噬细胞分化,这支持了淋巴瘤向组织细胞/树突状细胞肿瘤转分化的可能性。此外,在肿瘤组织细胞和邻近神经元中检测到SARS-CoV-2,这提出了病毒感染与肿瘤发展之间潜在相互作用的问题。结论:虽然潜在的机制仍不确定,但这一发现强调了进一步研究SARS-CoV-2感染与肿瘤发生之间相互作用的必要性。本病例是k18-hACE2小鼠中与SARS-CoV-2相关的原发性脑组织细胞淋巴细胞增生性疾病的首次报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Primary leptomeningeal histiocytic lymphoproliferative disorder associated with SARS-CoV-2 brain infection in k18-hACE2 mouse: a case report.

Primary leptomeningeal histiocytic lymphoproliferative disorder associated with SARS-CoV-2 brain infection in k18-hACE2 mouse: a case report.

Primary leptomeningeal histiocytic lymphoproliferative disorder associated with SARS-CoV-2 brain infection in k18-hACE2 mouse: a case report.

Primary leptomeningeal histiocytic lymphoproliferative disorder associated with SARS-CoV-2 brain infection in k18-hACE2 mouse: a case report.

Background: Histiocytic proliferative disorders in the central nervous system are rare, and their potential association with viral infections remains largely unexplored. This case is relevant because it suggests a potential interaction between SARS-CoV-2 neuroinvasion and tumor development, providing insights into how viral infections might influence oncogenesis.

Case presentation: A 4.5-month-old male k18-hACE-2 mouse, part of an experimental study of SARS-CoV-2, displayed a small mass in leptomeningeal area composed by neoplastic round cells. This process is associated with typical acute inflammatory and neurodegenerative lesions according to viral neuroinvasion. Histopathology revealed a well-demarcated tumor composed of lymphoblasts and intermixed with abundant histiocytic-like cells. Immunohistochemistry showed high expression of Iba-1 in histiocytes but negative PAX5, CD3 and IRF-4 labeling. Due to the critical role of PAX-5 in maintaining B-cell function, its reduction or inactivation may favor this loss of identity and differentiation to macrophages, which supports the possibility of a lymphoma undergoing transdifferentiation into a histiocytic/dendritic cells neoplasm. Additionally, SARS-CoV-2 was detected within the tumor histiocytes and adjacent neurons, raising questions about potential interactions between viral infection and tumor development.

Conclusions: While the underlying mechanisms remain uncertain, this finding highlights the need for further investigation into the interplay between SARS-CoV-2 infection and oncogenesis. This case represents the first report of a primary brain histiocytic lymphoproliferative disorder associated with SARS-CoV-2 in k18-hACE2 mouse.

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CiteScore
4.40
自引率
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