Khamlichi A A, Rocca A, Touchard G, Aucouturier P, Preud'homme J L, Cogné M
Laboratoire d'Immunologie et Génétique, CNRS URA 1172, IBMIG, Faculté des Sciences, Poitiers, France.
Blood. 1995 Nov 15;86(10):3655-9.
Light chain deposition disease (LCDD) results from a propensity of some human monoclonal L chains to form tissue deposits. We designed an experimental model for in vivo expression of human kappa L chain sequences in mice and compared a somatically mutated LCDD chain with a closely related control kappa chain, both encoded by the unique V kappa IV gene. Mice secreting the LCDD chain but not those producing the control chain showed deposits with a distribution similar to that observed in patients. These data show that discrete changes in V region sequences can play a major role in tissue deposition of human L chains.
轻链沉积病(LCDD)是由一些人源单克隆轻链形成组织沉积物的倾向所致。我们设计了一个在小鼠体内表达人κ轻链序列的实验模型,并比较了由独特的VκIV基因编码的体细胞突变的LCDD链与密切相关的对照κ链。分泌LCDD链的小鼠而非产生对照链的小鼠显示出沉积物,其分布与在患者中观察到的相似。这些数据表明V区序列的离散变化在人轻链的组织沉积中可起主要作用。