Dual Role of B Cells in Multiple Sclerosis

被引:16
作者
Kumar, Gaurav [1 ]
Axtell, Robert C. [1 ]
机构
[1] Oklahoma Med Res Fdn, Arthrit & Clin Immunol Res Program, Oklahoma City, OK 73104 USA
基金
美国国家卫生研究院;
关键词
multiple sclerosis; B cells; disease-modifying therapies; NECROSIS-FACTOR FAMILY; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; MATURATION ANTIGEN; DIFFERENTIAL-DIAGNOSIS; TNF RECEPTOR; DOUBLE-BLIND; BONE-MARROW; BAFF LEVELS; APRIL; BCMA;
D O I
10.3390/ijms24032336
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
B cells have emerged as an important immune cell type that can be targeted for therapy in multiple sclerosis (MS). Depleting B cells with anti-CD20 antibodies is effective in treating MS. Yet, atacicept treatment, which blocks B-cell Activating Factor (BAFF) and A Proliferation-Inducing Ligand (APRIL), two cytokines important for B cell development and function, paradoxically increases disease activity in MS patients. The reason behind the failure of atacicept is not well understood. The stark differences in clinical outcomes with these therapies demonstrate that B cells have both inflammatory and anti-inflammatory functions in MS. In this review, we summarize the importance of B cells in MS and discuss the different B cell subsets that perform inflammatory and anti-inflammatory functions and how therapies modulate B cell functions in MS patients. Additionally, we discuss the potential anti-inflammatory functions of BAFF and APRIL on MS disease.
引用
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页数:12
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