Gandoglia Ilaria, Ivaldi Federico, Laroni Alice, Benvenuto Federica, Solaro Claudio, Mancardi Gianluigi, Kerlero de Rosbo Nicole, Uccelli Antonio
Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health Unit (I.G., A.L., F.B., G.M., N.K.d.R., A.U.), and Center of Excellence for Biomedical Research (CEBR) (F.I., A.L., G.M., A.U.), University of Genoa, Italy; Ospedale Policlinico San Martino-IRCCS (A.L., G.M., A.U.), Genoa, Italy; and Rehabilitation Unit (C.S.), Centro di Recupero e Rieducazione Funzionale, M.L. Novarese, Moncrivello, Italy.
Neurol Neuroimmunol Neuroinflamm. 2017 Oct 23;4(6):e403. doi: 10.1212/NXI.0000000000000403. eCollection 2017 Nov.
To study the immunomodulatory effect of teriflunomide on innate and adaptive immune cell populations through a pilot, open-label, observational study in a cohort of patients with relapsing-remitting MS.
Blood lymphocytes were isolated from 10 patients with MS before and after 3 or 12 months of treatment. Adaptive and innate immune cell subsets were analyzed by flow cytometry as follows: B cells (memory, regulatory, and mature subsets), T cells (effector and regulatory subsets), and natural killer (NK) cells (CD56 and CD56 subsets).
Our results show that teriflunomide significantly reduces absolute counts of total CD19 B cells and mature and regulatory B-cell subsets. T cells were affected to a lesser extent, with a trend in reduction of absolute counts for both T effector CD4 cells (Th1, Th17 and Th1/17) and T regulatory CD8 and CD4 cells. Teriflunomide had no detectable effect on NK-cell numbers.
In our small cohort, teriflunomide treatment affects mainly and significantly on B-cell numbers, while having a milder effect on T-cell numbers. Larger cohorts are necessary to confirm these findings and understand the effect of teriflunomide on the functionality of these cells.
通过一项针对复发缓解型多发性硬化症患者队列的初步、开放标签观察性研究,探讨特立氟胺对先天性和适应性免疫细胞群体的免疫调节作用。
从10例多发性硬化症患者治疗前及治疗3个月或12个月后采集的血液中分离淋巴细胞。通过流式细胞术分析适应性和先天性免疫细胞亚群,具体如下:B细胞(记忆、调节和成熟亚群)、T细胞(效应和调节亚群)以及自然杀伤(NK)细胞(CD56和CD56亚群)。
我们的结果显示,特立氟胺显著降低了总CD19 B细胞以及成熟和调节性B细胞亚群的绝对计数。T细胞受到的影响较小,效应性CD4 T细胞(Th1、Th17和Th1/17)以及调节性CD8和CD4 T细胞的绝对计数有减少趋势。特立氟胺对NK细胞数量未产生可检测到的影响。
在我们的小队列研究中,特立氟胺治疗主要且显著影响B细胞数量,而对T细胞数量的影响较小。需要更大的队列来证实这些发现并了解特立氟胺对这些细胞功能的影响。