奥克列珠单抗
多发性硬化
CD20
炎症
医学
免疫学
生物标志物
细胞因子
抗体
生物
美罗华
生物化学
作者
Christian Curran,Gisela Vaitaitis,Dan Waid,Timothy Volmer,Enrique Alverez,David H. Wagner
标识
DOI:10.1016/j.jneuroim.2022.578008
摘要
Treating MS has been difficult. One successful drug is Ocrelizumab (anti-CD20), used for the chronic relapsing MS (RMS) and the progressive MS (PMS) forms. TH40 cells are pathogenic effector T cells that increase in percentage and numbers during chronic inflammation. Here we show that in the earliest MS course, clinically isolated syndrome (CIS), TH40 cells expand in number. In PMS TH40 cell numbers remain expanded demonstrating sustained chronic inflammation. In RMS TH40 cells were found in CSF and express CD20. Ocrelizumab reduced TH40 cells to healthy control levels in patients. During treatment inflammatory cytokine producing TH40 cells were decreased.
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