Longitudinally persistent cerebrospinal fluid B cells can resist treatment in multiple sclerosis

被引:28
作者
Greenfield, Ariele L. [1 ]
Dandekar, Ravi [1 ]
Ramesh, Akshaya [1 ]
Eggers, Erica L. [1 ,3 ]
Wu, Hao [1 ,4 ]
Laurent, Sarah [1 ,5 ]
Harkin, William [1 ,6 ]
Pierson, Natalie S. [1 ,7 ]
Weber, Martin S. [2 ]
Henry, Roland G. [1 ]
Bischof, Antje [1 ]
Cree, Bruce A. C. [1 ]
Hauser, Stephen L. [1 ]
Wilson, Michael R. [1 ]
Von Buedingen, H-Christian [1 ,8 ]
机构
[1] UCSF, Dept Neurol, UCSF Weill Inst Neurosci, San Francisco, CA USA
[2] Univ Med Ctr Gottingen, Inst Neuropathol, Dept Neurol, Gottingen, Germany
[3] Adapt Biotechnol Corp, San Francisco, CA USA
[4] Cambrian InnovaTech, Shenzhen, Guangdong, Peoples R China
[5] Univ Hosp Cologne, Dept Neurol, Cologne, Germany
[6] UCSD, Sch Med, La Jolla, CA USA
[7] Keck Sch Med USC, Los Angeles, CA USA
[8] F Hoffmann La Roche, Basel, Switzerland
关键词
RITUXIMAB TREATMENT; MEMORY; LYMPHOCYTE; MENINGES; OCRELIZUMAB; FOLLICLES; DIAGNOSIS; DEPLETION; THERAPY; DISEASE;
D O I
10.1172/jci.insight.126599
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
B cells are key contributors to chronic autoimmune pathology in multiple sclerosis (MS). Clonally related B cells exist in the cerebrospinal fluid (CSF), meninges, and CNS parenchyma of MS patients. We sought to investigate the presence of clonally related B cells over time by performing Ig heavy chain variable region repertoire sequencing on B cells from longitudinally collected blood and CSF samples of MS patients (n = 10). All patients were untreated at the time of the initial sampling; the majority (n = 7) were treated with immune-modulating therapies 1.2 (+/- 0.3 SD) years later during the second sampling, We found clonal persistence of B cells in the CSF of 5 patients; these B cells were frequently lg class-switched and CD27(+). Specific blood B cell subsets appear to provide input into CNS repertoires over time, We demonstrate complex patterns of clonal B cell persistence in CSF and blood, even in patients on immune-modulating therapy. Our findings support the concept that peripheral B cell activation and CNS-compartmentalized immune mechanisms can in part be therapy resistant.
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页数:12
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