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游离DNA的免疫调节特性

Immunoregulatory properties of cell free DNA.

作者信息

Ferrera Francesca, Altosole Tiziana, Tardito Samuele, Astone Giuseppina, Bernardi Cinzia, Parodi Alessia, Marini Chiara, Conteduca Giuseppina, Cichero Elena, Salis Annalisa, Arpesella Leonardo, Camporesi Laura, Lagazio Andrea, Rigo Valentina, Pigozzo Andrea, Damonte Gianluca, Fossa Paola, Fenoglio Daniela, De Palma Raffaele, Inghirami Giorgio, Filaci Gilberto

机构信息

Department of Internal Medicine (DIMI), University of Genoa, Genoa, Italy.

IRCCS, IRCCS San Martino, Genoa, Italy.

出版信息

Cell Mol Life Sci. 2025 Aug 26;82(1):320. doi: 10.1007/s00018-025-05862-y.

Abstract

Cell free DNA (cfDNA) is detectable at low concentrations in the plasma of healthy subjects and at high concentrations in disorders characterized by a high rate of necrotic events, such as tumors and vasculitis, leading to the release of necrotic DNA into the surrounding tissue and the bloodstream. Although cfDNA may act as a danger signal by binding to DNA sensors, triggering inflammation and immune responses, elevated cfDNA concentrations instead may exert immunoregulatory activities. Here, we show that exogenously administered cfDNA mediates immunoregulatory functions in vivo, in particular, it protects lupus-prone mice from disease progression and favors tumor growth in tumor-challenged mice. Our data suggest that cfDNA mediates immune regulatory activities by directly interacting with MHC class II molecules on antigen-presenting cells and through recruitment of regulatory T cells. This study unveils unprecedented biologic functions of cfDNA with significant pathogenic relevance and remarkable implications for the treatment of cancer patients.

摘要

游离DNA(cfDNA)在健康受试者的血浆中可检测到低浓度,而在以坏死事件发生率高为特征的疾病(如肿瘤和血管炎)中可检测到高浓度,这些疾病会导致坏死DNA释放到周围组织和血液中。尽管cfDNA可能通过与DNA传感器结合充当危险信号,触发炎症和免疫反应,但cfDNA浓度升高反而可能发挥免疫调节活性。在此,我们表明外源性给予的cfDNA在体内介导免疫调节功能,特别是,它保护易患狼疮的小鼠免于疾病进展,并有利于肿瘤攻击小鼠中的肿瘤生长。我们的数据表明,cfDNA通过与抗原呈递细胞上的MHC II类分子直接相互作用并通过募集调节性T细胞来介导免疫调节活性。这项研究揭示了cfDNA前所未有的生物学功能,具有重要的致病相关性,并对癌症患者的治疗具有显著意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a51/12381308/7056a03f2611/18_2025_5862_Fig1_HTML.jpg

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