Stone M J, Tong A W, Fay J W, Lee J C
Charles A. Sammons Cancer Center, Baylor University Medical Center, Dallas, TX 75246.
Cancer Detect Prev. 1988;12(1-6):621-35.
The monoclonal antibody MM4 reacts with human myeloma cells from plasma cell dyscrasia (PCD)-derived cell lines and bone marrow (BM) biopsies from PCD patients, but not with normal BM or peripheral blood mononuclear (PBM) cells. We examined cytotoxicity of MM4 and rabbit complement (MM4:C') on mixtures of normal BM mononuclear cells and myeloma cells from three different PCD-derived cell lines, RPMI 8226, GM 1312, or ARH-77. For cell preparations containing 10% myeloma cells, treatment with MM4 (500 micrograms per 10(5) cells, 4 degrees C, 60 min) and two cycles of complement (1:8, 23 degrees C, 2 x 30 min) consistently eliminated 2 logs or more of clonogenic myeloma stem cells, as determined by colony growth assays and limiting dilution analysis (99.4%, 98.9%, and 99.96% reduction of RPMI 8226, GM 1312, and ARH-77 cells, respectively). The majority of normal marrow progenitors were spared (inhibition of CFU-C: 10-13%; BFU-E: 0%). These observations suggest that MM4 may be useful for selective depletion of human myeloma clonogenic stem cells from bone marrow ex vivo.
单克隆抗体MM4可与浆细胞发育异常(PCD)衍生细胞系的人骨髓瘤细胞以及PCD患者的骨髓(BM)活检样本发生反应,但不与正常BM或外周血单个核(PBM)细胞发生反应。我们检测了MM4和兔补体(MM4:C')对来自三种不同PCD衍生细胞系(RPMI 8226、GM 1312或ARH-77)的正常BM单个核细胞与骨髓瘤细胞混合物的细胞毒性。对于含有10%骨髓瘤细胞的细胞制剂,用MM4(每10⁵个细胞500微克,4℃,60分钟)处理并进行两个补体循环(1:8,23℃,2×30分钟),通过集落生长测定和极限稀释分析确定,始终能消除2个对数或更多的克隆形成性骨髓瘤干细胞(RPMI 8226、GM 1312和ARH-77细胞分别减少99.4%、98.9%和99.96%)。大多数正常骨髓祖细胞得以保留(集落形成单位 - 粒细胞(CFU-C)抑制率:10 - 13%;爆式红系集落形成单位(BFU-E)抑制率:0%)。这些观察结果表明,MM4可能有助于在体外从骨髓中选择性清除人骨髓瘤克隆形成干细胞。