Barcos M, Kim S, Seon B K, Nussbaum A, Gailani S, Henderson E S
Med Pediatr Oncol. 1979;7(4):341-9. doi: 10.1002/mpo.2950070409.
A patient with multiple myeloma, IgG kappa type, developed erythroleukemia with cytogenetic abnormalities three years after diagnosis. The latter disease progressed terminally to acute granulocytic leukemia. Anti-idiotype antibody reagents were prepared by injecting rabbits with the purified monoclonal IgG kappa obtained from the patient's serum and subsequent absorption of the antisera with normal IgG coupled to Sepharose 4B. These reagents reacted specifically with autologous myeloma cells but failed to react with all tested allogeneic cells: these included myeloma cells, reactive lymphocytes and plasma cells, and established lymphoid cell lines. Common idiotypic determinants were found in lymphoid and plasmacytic cells of the patient's marrow, spleen, lymph node, and gastrointestinal tract at autopsy that were not present in the leukemic population. The findings indicate that myeloma and granulocytic leukemia cells have separate clonal origins.
一名IgG κ型多发性骨髓瘤患者在诊断三年后发生了伴有细胞遗传学异常的红白血病。后一种疾病最终进展为急性粒细胞白血病。通过用从患者血清中获得的纯化单克隆IgG κ免疫兔子,随后用偶联到琼脂糖4B上的正常IgG吸收抗血清来制备抗独特型抗体试剂。这些试剂与自体骨髓瘤细胞特异性反应,但与所有测试的异基因细胞均无反应:这些异基因细胞包括骨髓瘤细胞、反应性淋巴细胞和浆细胞以及已建立的淋巴细胞系。尸检时发现患者骨髓、脾脏、淋巴结和胃肠道的淋巴细胞和浆细胞中存在共同的独特型决定簇,而白血病细胞群体中不存在。这些发现表明骨髓瘤细胞和粒细胞白血病细胞有不同的克隆起源。