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奥瑞珠单抗的免疫调节作用和多发性硬化症治疗反应监测的候选生物标志物。

Immunomodulatory effects of ocrelizumab and candidate biomarkers for monitoring treatment response in multiple sclerosis.

机构信息

Second Division of Neurology, Department of Advanced Medical and Surgical Sciences, University of Campania Luigi Vanvitelli, Naples, Italy.

出版信息

Mult Scler. 2023 Jun;29(7):779-788. doi: 10.1177/13524585221147635. Epub 2023 Jan 22.

DOI:10.1177/13524585221147635
PMID:36683286
Abstract

Ocrelizumab is a humanized monoclonal antibody designed to bind to the CD20 molecule, resulting in a rapid depletion of B-cells; however, it has been shown that lymphocyte subpopulations other than B-cells are affected by the drug. To review the effects of ocrelizumab on circulating lymphocytes and identify candidate biomarkers to predict and monitor treatment response. A literature search for the most relevant articles from 2006 to 2022 was conducted in PubMed and Scopus. The effect of ocrelizumab on the peripheral immune system goes beyond B-cells; it also depletes T CD20 + lymphocytes. Further, ocrelizumab reshapes the T-cell response toward a low inflammatory profile and induces an increase in T CD8 + regulatory cell percentage. A higher Body Mass Index and higher B-cell count at baseline have been associated with early B-cell reappearance. Serum neurofilament light chain reduction has been associated with treatment response. Ocrelizumab treatment exerts a broad immunomodulatory effect and may be tailored based on patients' clinical and biological profiles.

摘要

奥瑞珠单抗是一种人源化单克隆抗体,旨在与 CD20 分子结合,导致 B 细胞迅速耗竭;然而,已经表明,除了 B 细胞以外,淋巴细胞亚群也受到药物的影响。为了综述奥瑞珠单抗对循环淋巴细胞的影响,并确定预测和监测治疗反应的候选生物标志物。在 PubMed 和 Scopus 中进行了 2006 年至 2022 年最相关文章的文献检索。奥瑞珠单抗对外周免疫系统的影响超出了 B 细胞;它还耗竭了 T CD20+淋巴细胞。此外,奥瑞珠单抗使 T 细胞反应向低炎症特征重塑,并诱导 T CD8+调节性细胞百分比增加。较高的体重指数和基线时较高的 B 细胞计数与早期 B 细胞重现有关。血清神经丝轻链减少与治疗反应相关。奥瑞珠单抗治疗产生广泛的免疫调节作用,并且可以根据患者的临床和生物学特征进行调整。

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Immunomodulatory effects of ocrelizumab and candidate biomarkers for monitoring treatment response in multiple sclerosis.奥瑞珠单抗的免疫调节作用和多发性硬化症治疗反应监测的候选生物标志物。
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J Neurol. 2025 Aug 16;272(9):582. doi: 10.1007/s00415-025-13297-5.
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