Bell P B, Rooney N, Bosanquet A G
Bath Cancer Research, University of Bath, Royal United Hospital, United Kingdom.
Cytometry. 1999 Jun 15;38(3):102-5.
Both B-cell chronic lymphocytic leukemia (CLL) and mantle cell lymphoma (MCL) are characterized by a lymphoproliferation of neoplastic CD5+ B-cells, but an accurate differential diagnosis between these two malignancies is vitally important for guiding treatment options. Because CD79a has been identified as a pan-B marker, we intended to use it in place of CD19 to identify B-cells and to use CD23 to distinguish between CLL and MCL in the leukemic phase. Anti-CD79a (clone ZL7.4) was used to detect the Igalpha/mb1 protein in fresh CD5+ B-lymphocytes by dual-channel flow cytometry. Expression of CD19 and CD23 were similarly assessed. As expected, CD19 was expressed in all specimens, whereas CD23 expression was zero in 3/4 MCLs, weak in 1/4 MCLs, and 2/8 CLLs (10-19%) and stronger in 6/8 CLLs (> or =45%). However, although all the CD19+/CD5+ cells of MCL expressed high CD79a levels, CD79a expression was negligible or absent in 8/8 CLL specimens (mean positivity for CD79a = 2.41 +/- 2.71%). CD79a (ZL7.4) levels may provide a more reliable distinction than CD23 levels between CLL and MCL. If these results hold up in a larger series, we recommend that the ZL7.4 antibody should be considered in routine marker panels for CLL and low-grade lymphoma.
B细胞慢性淋巴细胞白血病(CLL)和套细胞淋巴瘤(MCL)均以肿瘤性CD5⁺B细胞的淋巴细胞增殖为特征,但准确鉴别这两种恶性肿瘤对于指导治疗方案至关重要。由于CD79a已被确定为全B标志物,我们打算用它替代CD19来识别B细胞,并使用CD23区分白血病期的CLL和MCL。通过双通道流式细胞术,使用抗CD79a(克隆ZL7.4)检测新鲜CD5⁺B淋巴细胞中的Igalpha/mb1蛋白。同样评估CD19和CD23的表达。正如预期的那样,所有标本中均表达CD19,而在3/4的MCL中CD23表达为零,在1/4的MCL中表达较弱,在2/8的CLL中(10 - 19%)表达较弱,在6/8的CLL中(≥45%)表达较强。然而,尽管MCL的所有CD19⁺/CD5⁺细胞均高表达CD79a,但在8/8的CLL标本中CD79a表达可忽略不计或缺失(CD79a的平均阳性率 = 2.41 ± 2.71%)。与CD23水平相比,CD79a(ZL7.4)水平可能为CLL和MCL之间提供更可靠的区分。如果这些结果在更大规模的研究中得到证实,我们建议在CLL和低级淋巴瘤的常规标志物组合中考虑使用ZL7.4抗体。