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免疫失调作为不同免疫背景下淋巴瘤发生的主要原则。

Immune dysregulation as a leading principle for lymphoma development in diverse immunological backgrounds.

作者信息

Kolijn P Martijn, Langerak Anton W

机构信息

Laboratory Medical Immunology, Department of Immunology, Erasmus Medical Center, Rotterdam, the Netherlands.

Laboratory Medical Immunology, Department of Immunology, Erasmus Medical Center, Rotterdam, the Netherlands.

出版信息

Immunol Lett. 2023 Nov;263:46-59. doi: 10.1016/j.imlet.2023.08.007. Epub 2023 Sep 27.

Abstract

Lymphoma is a heterogeneous group of malignancies arising from lymphocytes, which poses a significant challenge in terms of diagnosis and treatment due to its diverse subtypes and underlying mechanisms. This review aims to explore the shared and distinct features of various forms of lymphoma predisposing conditions, with a focus on genetic, immunological and molecular aspects. While diseases such as autoimmune disorders, inborn errors of immunity and iatrogenic immunodeficiencies are biologically and immunologically distinct, each of these diseases results in profound immune dysregulation and a predisposition to lymphoma development. Interestingly, the increased risk is often skewed towards a particular subtype of lymphoma. Patients with inborn errors of immunity in particular present with extreme forms of lymphoma predisposition, providing a unique opportunity to study the underlying mechanisms. External factors such as chronic infections and environmental exposures further modulate the risk of lymphoma development. Common features of conditions predisposing to lymphoma include: persistent inflammation, recurrent DNA damage or malfunctioning DNA repair, impaired tumor surveillance and viral clearance, and dysregulation of fundamental cellular processes such as activation, proliferation and apoptosis. Our growing understanding of the underlying mechanisms of lymphomagenesis provides opportunities for early detection, prevention and tailored treatment of lymphoma development.

摘要

淋巴瘤是一组起源于淋巴细胞的异质性恶性肿瘤,由于其亚型多样且潜在机制复杂,在诊断和治疗方面构成了重大挑战。本综述旨在探讨各种淋巴瘤易感条件的共同特征和独特特征,重点关注遗传、免疫和分子方面。虽然自身免疫性疾病、先天性免疫缺陷和医源性免疫缺陷等疾病在生物学和免疫学上各不相同,但这些疾病都会导致严重的免疫失调,并易患淋巴瘤。有趣的是,风险增加往往偏向于淋巴瘤的特定亚型。特别是先天性免疫缺陷患者表现出极高的淋巴瘤易感性,这为研究潜在机制提供了独特的机会。慢性感染和环境暴露等外部因素进一步调节淋巴瘤发生的风险。淋巴瘤易感条件的共同特征包括:持续性炎症、反复的DNA损伤或DNA修复功能障碍、肿瘤监测和病毒清除受损,以及激活、增殖和凋亡等基本细胞过程的失调。我们对淋巴瘤发生潜在机制的日益了解为淋巴瘤的早期检测、预防和个性化治疗提供了机会。

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