Theus Michelle H
Department of Biomedical Sciences and Pathobiology, Virginia Tech, Blacksburg, VA, United States.
Center for Engineered Health, Virginia Tech, Blacksburg, VA, United States.
Front Neurol. 2024 Feb 21;15:1334847. doi: 10.3389/fneur.2024.1334847. eCollection 2024.
Acquired traumatic central nervous system (CNS) injuries, including traumatic brain injury (TBI) and spinal cord injury (SCI), are devastating conditions with limited treatment options. Neuroinflammation plays a pivotal role in secondary damage, making it a prime target for therapeutic intervention. Emerging therapeutic strategies are designed to modulate the inflammatory response, ultimately promoting neuroprotection and neuroregeneration. The use of anti-inflammatory agents has yielded limited support in improving outcomes in patients, creating a critical need to re-envision novel approaches to both quell deleterious inflammatory processes and upend the progressive cycle of neurotoxic inflammation. This demands a comprehensive exploration of individual, age, and sex differences, including the use of advanced imaging techniques, multi-omic profiling, and the expansion of translational studies from rodents to humans. Moreover, a holistic approach that combines pharmacological intervention with multidisciplinary neurorehabilitation is crucial and must include both acute and long-term care for the physical, cognitive, and emotional aspects of recovery. Ongoing research into neuroinflammatory biomarkers could revolutionize our ability to predict, diagnose, and monitor the inflammatory response in real time, allowing for timely adjustments in treatment regimens and facilitating a more precise evaluation of therapeutic efficacy. The management of neuroinflammation in acquired traumatic CNS injuries necessitates a paradigm shift in our approach that includes combining multiple therapeutic modalities and fostering a more comprehensive understanding of the intricate neuroinflammatory processes at play.
获得性创伤性中枢神经系统(CNS)损伤,包括创伤性脑损伤(TBI)和脊髓损伤(SCI),是具有毁灭性的病症,治疗选择有限。神经炎症在继发性损伤中起关键作用,使其成为治疗干预的主要靶点。新兴的治疗策略旨在调节炎症反应,最终促进神经保护和神经再生。抗炎药物在改善患者预后方面的支持有限,因此迫切需要重新设想新的方法来平息有害的炎症过程,并打破神经毒性炎症的进展循环。这需要全面探索个体、年龄和性别差异,包括使用先进的成像技术、多组学分析,以及将转化研究从啮齿动物扩展到人类。此外,将药物干预与多学科神经康复相结合的整体方法至关重要,并且必须包括对身体、认知和情感恢复方面的急性和长期护理。对神经炎症生物标志物的持续研究可能会彻底改变我们实时预测、诊断和监测炎症反应的能力,从而能够及时调整治疗方案,并有助于更精确地评估治疗效果。获得性创伤性中枢神经系统损伤中神经炎症的管理需要我们转变方法,包括结合多种治疗方式,并更全面地了解所涉及的复杂神经炎症过程。