Boșca Adina Bianca, Dinte Elena, Mihu Carmen Mihaela, Pârvu Alina Elena, Melincovici Carmen Stanca, Șovrea Alina Simona, Mărginean Mariana, Constantin Anne-Marie, Băbțan Anida-Maria, Muntean Alexandrina, Ilea Aranka
Department of Histology, Faculty of Medicine, "Iuliu Hațieganu" University of Medicine and Pharmacy, 400012 Cluj-Napoca, Romania.
Department of Pharmaceutical Technology and Biopharmaceutics, Faculty of Pharmacy, "Iuliu Hațieganu" University of Medicine and Pharmacy, 400012 Cluj-Napoca, Romania.
Pharmaceutics. 2024 Sep 6;16(9):1175. doi: 10.3390/pharmaceutics16091175.
Periodontitis is a chronic inflammation caused by periodontopathogenic bacteria in the dental biofilm, and also involves the inflammatory-immune response of the host. Polymorphonuclear neutrophils (PMNs) play essential roles in bacterial clearance by multiple mechanisms, including the formation of neutrophil extracellular traps (NETs) that retain and destroy pathogens. During PD progression, the interaction between PMNs, NETs, and bacteria leads to an exaggerated immune response and a prolonged inflammatory state. As a lesion matures, PMNs accumulate in the periodontal tissues and die via NETosis, ultimately resulting in tissue injury. A better understanding of the role of NETs, the associated molecules, and the pathogenic pathways of NET formation in periodontitis, could provide markers of NETosis as reliable diagnostic and prognostic tools. Moreover, an assessment of NET biomarker levels in biofluids, particularly in saliva or gingival crevicular fluid, could be useful for monitoring periodontitis progression and treatment efficacy. Preventing excessive NET accumulation in periodontal tissues, by both controlling NETs' formation and their appropriate removal, could be a key for further development of more efficient therapeutic approaches. In periodontal therapy, local drug delivery (LDD) systems are more targeted, enhancing the bioavailability of active pharmacological agents in the periodontal pocket and surrounding tissues for prolonged time to ensure an optimal therapeutic outcome.
牙周炎是由牙菌斑中的牙周致病细菌引起的慢性炎症,也涉及宿主的炎症免疫反应。多形核中性粒细胞(PMN)通过多种机制在清除细菌中发挥重要作用,包括形成保留并破坏病原体的中性粒细胞胞外陷阱(NET)。在牙周炎进展过程中,PMN、NET与细菌之间的相互作用导致过度的免疫反应和持久的炎症状态。随着病变成熟,PMN在牙周组织中积聚并通过NETosis死亡,最终导致组织损伤。更好地了解NET在牙周炎中的作用、相关分子以及NET形成的致病途径,可为NETosis提供可靠的诊断和预后工具的标志物。此外,评估生物流体(特别是唾液或龈沟液)中的NET生物标志物水平,可能有助于监测牙周炎的进展和治疗效果。通过控制NET的形成及其适当清除来防止NET在牙周组织中过度积聚,可能是进一步开发更有效治疗方法的关键。在牙周治疗中,局部给药(LDD)系统更具针对性,可提高活性药物在牙周袋和周围组织中的生物利用度,并延长时间以确保最佳治疗效果。