Thakolwiboon Smathorn, Mills Elizabeth A, Yang Jennifer, Doty Jonathan, Belkin Martin I, Cho Thomas, Schultz Charles, Mao-Draayer Yang
Department of Neurology, University of Michigan, Ann Arbor, MI, United States.
Michigan Institute for Neurological Disorders, Farmington Hills, MI, United States.
Front Aging. 2023 Oct 13;4:1234572. doi: 10.3389/fragi.2023.1234572. eCollection 2023.
Aging is associated with a progressive decline of innate and adaptive immune responses, called immunosenescence. This phenomenon links to different multiple sclerosis (MS) disease courses among different age groups. While clinical relapse and active demyelination are mainly related to the altered adaptive immunity, including invasion of T- and B-lymphocytes, impairment of innate immune cell (e.g., microglia, astrocyte) function is the main contributor to disability progression and neurodegeneration. Most patients with MS manifest the relapsing-remitting phenotype at a younger age, while progressive phenotypes are mainly seen in older patients. Current disease-modifying therapies (DMTs) primarily targeting adaptive immunity are less efficacious in older patients, suggesting that immunosenescence plays a role in treatment response. This review summarizes the recent immune mechanistic studies regarding immunosenescence in patients with MS and discusses the clinical implications of these findings.
衰老与先天性和适应性免疫反应的进行性衰退有关,称为免疫衰老。这种现象与不同年龄组的多种不同多发性硬化症(MS)病程相关。虽然临床复发和活跃的脱髓鞘主要与适应性免疫改变有关,包括T淋巴细胞和B淋巴细胞的侵入,但先天性免疫细胞(如小胶质细胞、星形胶质细胞)功能受损是残疾进展和神经退行性变的主要原因。大多数MS患者在年轻时表现为复发缓解型表型,而进展型表型主要见于老年患者。目前主要针对适应性免疫的疾病修正疗法(DMTs)在老年患者中疗效较差,这表明免疫衰老在治疗反应中起作用。本综述总结了近期关于MS患者免疫衰老的免疫机制研究,并讨论了这些发现的临床意义。