Haegert D G, Stuart J, Smith J L
Br Med J. 1975 Feb 8;1(5953):312-4. doi: 10.1136/bmj.1.5953.312.
By using several techniques to detect surface markers on T and B lymphocytes, 11 cases of acute lymphoblastic leukaemia (A.L.L.) were studied. In four cases an insignificant number of markers were detected on the lymphoblast populations. In one case a significant number of blasts formed both sheep red blood cell rosettes and Fc rosettes, suggesting a T-cell origin for the neoplastic cells, and in another case the presence of Fc and C3 receptors on the lymphoblast population indicated a B-cell origin. In a further five cases 14-43% of the blasts had detectable surface immunoglobulin. It is concluded that A.L.L. is a heterogeneous disorder, some cases failing to express surface markers and others having either a T-or a B-lymphocyte origin or both.
通过运用多种技术检测T和B淋巴细胞表面标志物,对11例急性淋巴细胞白血病(A.L.L.)进行了研究。在4例中,在淋巴母细胞群体上检测到的标志物数量微不足道。在1例中,大量母细胞形成了绵羊红细胞玫瑰花结和Fc玫瑰花结,提示肿瘤细胞起源于T细胞;在另一例中,淋巴母细胞群体上存在Fc和C3受体表明起源于B细胞。在另外5例中,14% - 43%的母细胞具有可检测到的表面免疫球蛋白。得出的结论是,急性淋巴细胞白血病是一种异质性疾病,一些病例不表达表面标志物,而另一些病例起源于T淋巴细胞或B淋巴细胞,或两者皆有。