Ritchie Alanna M, Gilden Donald H, Williamson R Anthony, Burgoon Mark P, Yu Xiaoli, Helm Karen, Corboy John R, Owens Gregory P
Department of Neurology, University of Colorado Cancer Center, University of Colorado Health Sciences Center, Denver, CO 80262, USA.
J Immunol. 2004 Jul 1;173(1):649-56. doi: 10.4049/jimmunol.173.1.649.
Increased amounts of intrathecally synthesized IgG and oligoclonal bands have long been recognized as a hallmark of multiple sclerosis (MS). B cells and plasma cells are components of the inflammatory infiltrates in both active and chronic MS lesions, and increased numbers of these cells are present in MS cerebrospinal fluid (CSF). Single-cell RT-PCR was used to analyze both the CD19+ B cell and CD138+ plasma cell populations in CSF of two patients with clinically definite MS and of one MS patient whose CSF was obtained after a clinically isolated syndrome, but before the second episode. Sequence analysis of amplified IgG V region sequences identified the rearranged germline segments, extent of somatic mutation, and clonal relationships within and between the two cell populations in the three MS patients. Expanded B cell and plasma cell clones were detected in each MS CSF and in all three patients the CD138+ IgG repertoire was more restricted. However, little if any significant sequence overlap was observed between the CD19+ and CD138+ repertoires of each donor. Detection of plasma cell clones by single-cell PCR will facilitate the in vitro production of recombinant Abs useful in identifying disease-relevant Ags.
鞘内合成的IgG量增加和寡克隆带长期以来一直被认为是多发性硬化症(MS)的一个标志。B细胞和浆细胞是活动性和慢性MS病变中炎性浸润的组成部分,并且这些细胞数量的增加存在于MS脑脊液(CSF)中。使用单细胞逆转录聚合酶链反应(RT-PCR)分析了两名临床确诊MS患者以及一名在临床孤立综合征后但在第二次发作前获取CSF的MS患者CSF中的CD19+B细胞和CD138+浆细胞群体。对扩增的IgG V区序列进行序列分析,确定了三位MS患者两个细胞群体内部和之间重排的种系区段、体细胞突变程度以及克隆关系。在每个MS患者的CSF中均检测到了扩增的B细胞和浆细胞克隆,并且在所有三位患者中,CD138+IgG谱系更为受限。然而,在每个供体的CD19+和CD138+谱系之间几乎未观察到任何显著的序列重叠。通过单细胞PCR检测浆细胞克隆将有助于体外生产可用于鉴定疾病相关抗原的重组抗体。