Stevenson F K, Morris D, Stevenson G T
Immunology. 1980 Oct;41(2):313-21.
The cells of the B lymphocytic leukaemia (L2C) of strain 2 guinea-pigs have IgM on their surfaces but produce insufficient monoclonal IgM in vivo to be detectable by conventional serum electrophoresis. A radioimmunoassay, using anti-idiotypic antibody raised against the surface IgM of these cells, has been used to estimate levels of extracellular IgM produced both in vitro and in vivo. Analyses of the contributions to such IgM from the cell surface and from an export pathway have been made by examining the effect of prior removal of surface Fab mu by papain, and by following the fate of radio-iodinated surface IgM. Results suggest that the extracellular IgM arises predominantly from an export pathway, being exported in both pentameric and monomeric forms. Only a minute contribution, possibly in the form of vesicle-bound monomeric IgM, appears to derive from the cell surface. Radioimmunoassay was used to monitor the increasing levels of this leukaemic cell product during the course of the disease. Idiotypic IgM was detectable when the body load of neoplastic cells was approximately 4% of that detectable by an increased white cell count in the blood.
2系豚鼠的B淋巴细胞白血病(L2C)细胞表面有IgM,但在体内产生的单克隆IgM不足以通过传统血清电泳检测到。一种放射免疫测定法,使用针对这些细胞表面IgM产生的抗独特型抗体,已被用于估计体外和体内产生的细胞外IgM水平。通过检查木瓜蛋白酶预先去除表面Fabμ的效果,以及追踪放射性碘化表面IgM的命运,分析了细胞表面和输出途径对这种IgM的贡献。结果表明,细胞外IgM主要来自输出途径,以五聚体和单体形式输出。似乎只有极少量的贡献,可能是以囊泡结合的单体IgM形式,来自细胞表面。放射免疫测定法用于监测这种白血病细胞产物在疾病过程中的水平升高。当肿瘤细胞的体内负荷约为血液中白细胞计数增加可检测到的负荷的4%时,可检测到独特型IgM。