Nielsen Birgitte Romme, Ratzer Rikke, Börnsen Lars, von Essen Marina Rode, Christensen Jeppe Romme, Sellebjerg Finn
Danish Multiple Sclerosis Center, Department of Neurology, Rigshopitalet, University of Copenhagen, Denmark.
Danish Multiple Sclerosis Center, Department of Neurology, Rigshopitalet, University of Copenhagen, Denmark.
J Neuroimmunol. 2017 Sep 15;310:17-25. doi: 10.1016/j.jneuroim.2017.06.001. Epub 2017 Jun 3.
We characterized naïve, central memory (CM), effector memory (EM) and terminally differentiated effector memory (TEMRA) CD4 and CD8 T cells and their expression of CD49d and CD26 in peripheral blood in patients with multiple sclerosis (MS) and healthy controls. CD26 CD28 CD4 TEMRA T cells were increased in all subtypes of MS, and CD26 CD28 CD8 TEMRA T cells were increased in relapsing-remitting and secondary progressive MS. Conversely, in progressive MS, CD49d CM T cells were decreased and natalizumab increased the circulating number of all six subsets but reduced the frequency of most subsets expressing CD49d and CD26.
我们对多发性硬化症(MS)患者和健康对照者外周血中的初始、中枢记忆(CM)、效应记忆(EM)和终末分化效应记忆(TEMRA)CD4和CD8 T细胞及其CD49d和CD26的表达进行了表征。CD26⁺CD28⁻CD4⁺ TEMRA T细胞在MS的所有亚型中均增加,CD26⁺CD28⁻CD8⁺ TEMRA T细胞在复发缓解型和继发进展型MS中增加。相反,在进展型MS中,CD49d⁺ CM T细胞减少,那他珠单抗增加了所有六个亚群的循环数量,但降低了大多数表达CD49d和CD26的亚群的频率。