Niino Masaaki, Bodner Caroline, Simard Marie-Lune, Alatab Sudabeh, Gano Dawn, Kim Ho Jin, Trigueiro Manuela, Racicot Denise, Guérette Christine, Antel Jack P, Fournier Alyson, Grand'Maison Francois, Bar-Or Amit
Department of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Quebec, Canada.
Ann Neurol. 2006 May;59(5):748-54. doi: 10.1002/ana.20859.
Our objective was to study in vivo biological effects of natalizumab on immune cell phenotype and function in multiple sclerosis (MS) patients.
Blood was obtained before and after serial monthly natalizumab infusions to track functional expression of VLA-4 and migratory capacity of immune cells. The impact of infusion on activation thresholds of immune cells was evaluated.
Preinfusion VLA-4 expression differed across immune cell subsets. Natalizumab significantly, albeit partially, diminished VLA-4 expression on circulating immune cells. Cell subsets were differentially affected. Treatment significantly decreased migratory capacity of immune cells, correlating well with changes in VLA-4 expression. Effects of a single dose were not saturating and did not persist through the monthly dose interval. Infusion effect varied across patients but was remarkably stable in individual patients, over multiple infusions. Treatment significantly modulated proliferative responses of immune cells.
To our knowledge, we provide first proof of concept that natalizumab diminishes migratory capacity of immune cells. Our prospective study further shows that effects of therapy likely (1) differ for distinct immune cell subsets, (2) are not sustained over current dose interval, (3) have unique profiles in individual patients, and (4) include modulation of activation threshold of immune cells. Monitoring these parameters could be relevant to ongoing safety and efficacy considerations.
我们的目的是研究那他珠单抗对多发性硬化症(MS)患者免疫细胞表型和功能的体内生物学效应。
在每月连续输注那他珠单抗之前和之后采集血液,以追踪VLA-4的功能表达和免疫细胞的迁移能力。评估输注对免疫细胞激活阈值的影响。
输注前VLA-4表达在不同免疫细胞亚群中有所不同。那他珠单抗显著但部分地降低了循环免疫细胞上VLA-4的表达。细胞亚群受到的影响存在差异。治疗显著降低了免疫细胞的迁移能力,这与VLA-4表达的变化密切相关。单剂量的效果未达到饱和,且在每月剂量间隔内未持续存在。输注效果在不同患者中有所不同,但在个体患者中多次输注时非常稳定。治疗显著调节了免疫细胞的增殖反应。
据我们所知,我们首次提供了那他珠单抗降低免疫细胞迁移能力的概念验证。我们的前瞻性研究进一步表明,治疗效果可能(1)在不同免疫细胞亚群中有所不同,(2)在当前剂量间隔内不能持续,(3)在个体患者中有独特的表现,(4)包括调节免疫细胞的激活阈值。监测这些参数可能与正在进行的安全性和有效性考虑相关。