头颈鳞癌口腔黏膜炎中微生物与免疫互作研究进展

Research progress on microbial-host immune interplay in head and neck squamous cell carcinoma-related oral mucositis

  • 摘要: 口腔黏膜炎(oral mucositis,OM)是头颈鳞癌(head and neck squamous cell carcinoma,HNSCC)治疗中常见的并发症,目前仍然缺乏有效的治疗策略。放化疗性口腔黏膜炎(radiotherapy-induced OM,RIOM/chemotherapy-induced OM,CIOM)在头颈癌放疗患者中的发生率高达90%。目前的治疗方法主要集中在营养支持、疼痛控制和预防继发感染等在内的减轻症状和预防并发症手段。口腔微生物群在维持口腔功能性稳态、调控微环境及影响口腔疾病进展的过程中发挥重要作用。微生物与宿主之间相互作用,维持着口腔微生态的动态平衡。从免疫学的角度来看,OM的发生发展可能与口腔微生物群的改变和宿主免疫系统在口腔局部的免疫应答类型有关。然而,微生物与免疫相互调控的具体机制、微生物与免疫失衡状态下引发的不良反应,以及其在OM发展中发挥的关键作用尚未得到充分阐明。本文旨在深入探讨口腔微生物与宿主免疫系统的相互作用机制,特别是表观遗传学在其中的作用,以期加深对HNSCC相关OM病理生理学机制的理解。这些机制的阐述可能会揭示未来新型生物疗法的潜在靶点。

     

    Abstract: Oral mucositis (OM) is a common complication in head and neck squamous cell carcinoma (HNSCC) treatment, and no effective treatment strategies are currently available. The incidence of radiotherapy-induced OM (RIOM) and chemotherapy-induced OM (CIOM) in patients with head and neck cancer incidence rate is as high as 90%. The current treatment methods, including nutritional support, pain control, and prevention of secondary infections, are mainly focused on alleviating symptoms and preventing complications. The oral microbiota play a crucial role in maintaining the functional homeostasis of the oral cavity, regulating the microenvironment, and influencing the progression of oral diseases. The interaction between microorganisms and the host regulates the dynamics of the oral microbiome. Although the development and presence of OM is generally related to changes in the oral microbiota and the type of host immune response in the oral cavity, specific mechanisms underlying mutual microorganism-immune cell regulation, adverse reactions resulting from imbalanced microorganisms-immunity interaction, and their key roles in OM development have not been fully elucidated. This study aimed to elucidate the mechanisms underlying oral microbiota-host immune system interaction, focusing on the epigenetics regulation of OM that contributes to its pathophysiological mechanisms in HNSCC. Elucidating these mechanisms may reveal potential targets for novel biological therapy development.

     

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