Departments of Neurology and Ophthalmology, Programs in Neuroscience and Immunology, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, Colorado, USA.
Neurology, Laboratory Medicine and Pathology, Center for Multiple Sclerosis and Autoimmune Neurology, Mayo Clinic, Rochester, Minnesota, USA.
Ann Clin Transl Neurol. 2024 Oct;11(10):2792-2798. doi: 10.1002/acn3.52171. Epub 2024 Sep 2.
This post hoc analysis of the randomized, placebo-controlled N-MOmentum study (NCT02200770) of inebilizumab in neuromyelitis optica spectrum disorder (NMOSD) evaluated relationships between circulating B-cell subsets and aquaporin-4 immunoglobulin G (AQP4-lgG) titers and attacks. Among participants receiving placebo, CD20 and CD27 B-cell counts were modestly increased from the pre-attack visit to attack; plasmablast/plasma cell gene signature was increased from baseline to the pre-attack visit (p = 0.016) and from baseline to attack (p = 0.009). With inebilizumab treatment, B-cell subset counts decreased and did not increase with attacks. No difference in change of AQP4-IgG titers from baseline to time of attack was observed.
本事后分析对随机、安慰剂对照的 N-MOmentum 研究(NCT02200770)进行评估,该研究评估了视神经脊髓炎谱系疾病(NMOSD)中伊奈利珠单抗治疗中循环 B 细胞亚群与水通道蛋白 4 免疫球蛋白 G(AQP4-IgG)滴度和发作之间的关系。在接受安慰剂的参与者中,从发作前就诊到发作时,CD20 和 CD27 B 细胞计数略有增加;从基线到发作前就诊时,浆母细胞/浆细胞基因特征增加(p=0.016),从基线到发作时也增加(p=0.009)。使用伊奈利珠单抗治疗时,B 细胞亚群计数下降,且不因发作而增加。从基线到发作时的 AQP4-IgG 滴度变化无差异。