Abe Daijiro, Nakaseko Chiaki, Takeuchi Masahiro, Tanaka Hiroaki, Ohwada Chikako, Sakaida Emiko, Takeda Yusuke, Oda Kayo, Ozawa Shinichi, Shimizu Naomi, Masuda Shinichi, Cho Ryuko, Nishimura Miki, Misawa Sonoko, Kuwabara Satoshi, Saito Yasushi
Division of Hematology, Department of Clinical Cell Biology, Chiba University Graduate School of Medicine, Chiba, Japan.
Blood. 2008 Aug 1;112(3):836-9. doi: 10.1182/blood-2007-12-126979. Epub 2008 May 22.
POEMS syndrome is a rare plasma cell disorder characterized by peripheral neuropathy, monoclonal gammopathy, and high levels of serum vascular endothelial growth factor, the pathogenesis of which remains unclear. A unique feature of this syndrome is that the proliferating monoclonal plasma cells are essentially lambda-restricted. Here we determined complete nucleotide sequences of monoclonal immunoglobulin lambda light chain (IGL) variable regions in 11 patients with POEMS syndrome. The V-region of the Ig lambda gene of all 11 patients was restricted to the V lambda 1 subfamily. Searching for homologies with IGL germlines revealed that 2 germlines, IGLV1-4401 (9/11) and IGLV1-4001 (2/10), were identified, with an average homology of 91.1%. The IGLJ3*02 gene was used in 11 of 11 re-arrangements with an average homology of 92.2%. These data suggest that the highly restricted use of IGL V lambda 1 germlines plays an important role in the pathogenesis of POEMS syndrome.
POEMS综合征是一种罕见的浆细胞疾病,其特征为周围神经病变、单克隆丙种球蛋白病以及血清血管内皮生长因子水平升高,其发病机制尚不清楚。该综合征的一个独特特征是增殖的单克隆浆细胞主要受λ限制。在此,我们测定了11例POEMS综合征患者单克隆免疫球蛋白λ轻链(IGL)可变区的完整核苷酸序列。所有11例患者的Igλ基因V区均局限于Vλ1亚家族。与IGL种系进行同源性搜索发现,鉴定出2种种系,即IGLV1-4401(9/11)和IGLV1-4001(2/10),平均同源性为91.1%。11例重排中有11例使用了IGLJ3*02基因,平均同源性为92.2%。这些数据表明,IGL Vλ1种系的高度受限使用在POEMS综合征的发病机制中起重要作用。