Shih L Y, Chang C Y
Blut. 1985 Apr;50(4):225-32. doi: 10.1007/BF00320299.
We used the human placental conditioned medium stimulated single layer agar culture technique to study the in vitro growth of marrow cells from 62 adult patients with acute myeloid leukemia (AML). Bone marrow cells were cultured from 50 patients at the time of initial diagnosis, 19 patients in early remission and 20 patients during their full complete remission. Marrow cultures from untreated patients exhibited heterogeneous growth patterns ranging from complete growth failure to excessive microcluster formation. We classified the growth patterns into 4 groups: (1) Gr I: normal growth, (2) Gr II: no growth, (3) Gr III: decreased growth, (4) Gr IV: excessive growth of microclusters. At presentation, none had Gr I growth; Gr II growth was observed in 23; Gr III in 14 and Gr IV in 13. A predominance of no growth were seen in M1 and M3 subtypes, while Gr IV growth was more commonly observed in M2 or M4 subtype. We were unable to correlate the culture findings with age or white cell count. The present results not only indicated that AML at diagnosis was characterized by abnormal granulopoiesis but also demonstrated that leukemic progenitor cells were heterogeneous with different capacities to express their proliferating potential in vitro. Except few with decreased growth, the growth characteristics generally returned to normal with successful remission induction. Both Gr II and Gr IV growth patterns were not observed either in early remission or during full complete remission.
我们采用人胎盘条件培养基刺激单层琼脂培养技术,研究了62例成年急性髓系白血病(AML)患者骨髓细胞的体外生长情况。分别从50例初诊患者、19例早期缓解患者和20例完全缓解患者中获取骨髓细胞进行培养。未经治疗患者的骨髓培养呈现出从完全生长失败到过度微集落形成的多种不同生长模式。我们将生长模式分为4组:(1)I组:正常生长;(2)II组:无生长;(3)III组:生长减少;(4)IV组:微集落过度生长。初诊时,无I组生长情况;23例为II组生长;14例为III组生长;13例为IV组生长。M1和M3亚型中无生长情况占优势,而M2或M4亚型中IV组生长更为常见。我们无法将培养结果与年龄或白细胞计数相关联。目前的结果不仅表明初诊时的AML具有异常粒细胞生成的特征,还证明白血病祖细胞具有异质性,在体外表达增殖潜能的能力不同。除少数生长减少的情况外,随着缓解诱导成功,生长特征通常恢复正常。在早期缓解期或完全缓解期均未观察到II组和IV组生长模式。