Pfnür Andreas, Mayer Benjamin, Dörfer Lena, Tumani Hayrettin, Spitzer Daniel, Huber-Lang Markus, Kapapa Thomas
Department of Neurosurgery, University Hospital Ulm, Albert-Einstein-Allee 23, 89081 Ulm, Germany.
Institute of Epidemiology and Medical Biometry, University of Ulm, Helmholtzstr. 22, 89081 Ulm, Germany.
Int J Mol Sci. 2025 Feb 1;26(3):1276. doi: 10.3390/ijms26031276.
Aneurysmal subarachnoid hemorrhage (SAH) involves a significant influx of blood into the cerebrospinal fluid, representing a severe form of stroke. Despite advancements in aneurysm closure and neuro-intensive care, outcomes remain impaired due to cerebral vasospasm and delayed cerebral ischemia (DCI). Previous pharmacological therapies have not successfully reduced DCI while improving overall outcomes. As a result, significant efforts are underway to better understand the cellular and molecular mechanisms involved. This review focuses on the activation and effects of immune cells after SAH and their interactions with neurotoxic and vasoactive substances as well as inflammatory mediators. Particular attention is given to clinical studies highlighting the roles of natural killer (NK) cells and regulatory T cells (Treg) cells. Alongside microglia, astrocytes, and oligodendrocytes, NK cells and Treg cells are key contributors to the inflammatory cascade following SAH. Their involvement in modulating the neuro-inflammatory response, vasospasm, and DCI underscores their potential as therapeutic targets and prognostic markers in the post-SAH recovery process. We conducted a systematic review on T cell- and natural killer cell-mediated inflammation and their roles in cerebral vasospasm and delayed cerebral ischemia. We conducted a meta-analysis to evaluate outcomes and mortality in studies focused on NK cell- and T cell-mediated mechanisms.
动脉瘤性蛛网膜下腔出血(SAH)涉及大量血液流入脑脊液,是一种严重的中风形式。尽管在动脉瘤闭塞和神经重症监护方面取得了进展,但由于脑血管痉挛和迟发性脑缺血(DCI),预后仍然不佳。先前的药物治疗未能成功减少DCI,同时改善总体预后。因此,人们正在做出巨大努力,以更好地了解其中涉及的细胞和分子机制。本综述重点关注SAH后免疫细胞的激活和作用,以及它们与神经毒性和血管活性物质以及炎症介质的相互作用。特别关注突出自然杀伤(NK)细胞和调节性T细胞(Treg)细胞作用的临床研究。与小胶质细胞、星形胶质细胞和少突胶质细胞一样,NK细胞和Treg细胞是SAH后炎症级联反应的关键促成因素。它们参与调节神经炎症反应、血管痉挛和DCI,突出了它们作为SAH后恢复过程中治疗靶点和预后标志物的潜力。我们对T细胞和自然杀伤细胞介导的炎症及其在脑血管痉挛和迟发性脑缺血中的作用进行了系统综述。我们进行了一项荟萃分析,以评估专注于NK细胞和T细胞介导机制的研究中的预后和死亡率。