Martinez-Lostao Luis, Briones Javier, Martinez-Gallo Monica, Forné Ignasi, Sierra Jordi, Rodriguez-Sanchez Jose Luis, Juarez Candido
Immunology Department, Hospital de Sant Pau, Universitat Autonoma de Barcelona, Barcelona, Spain.
Leuk Lymphoma. 2004 Nov;45(11):2307-14. doi: 10.1080/10428190410001712216.
B-cell chronic lymphocytic leukemia (B-CLL) is a hematological malignancy characterized by the accumulation of mature CD5+ B lymphocytes with a defective apoptosis. A subset of blood monocyte-derived adherent cells generated in vitro protects B-CLL cells from apoptosis playing a role as nurse-like cells (NLCs). Fludarabine (9-beta-D-arabinofuranosyl-2-fluoroadenine; F-ara-A) is an adenine nucleoside analog used to treat B-CLL. To gain insight into the mechanisms implicated in the antitumoral effect of fludarabine in B-CLL cells, we performed cross-cultures with B-CLL cells and NLCs treated and untreated with fludarabine. Our results showed that fludarabine blocked the development of NLCs and induced apoptosis in these cells when they were present in culture. Moreover, CD19+/CD5+B-CLL cells treated with fludarabine underwent apoptosis and this event was not related with the presence of NLCs whether treated or not with fludarabine. In conclusion, apoptosis induced by fludarabine in CD19+/CD5+B-CLL cells was due to a direct effect on these cells and not due to its effect in the NLCs.
B 细胞慢性淋巴细胞白血病(B-CLL)是一种血液系统恶性肿瘤,其特征为成熟的 CD5+ B 淋巴细胞积累且凋亡存在缺陷。体外产生的一部分血液单核细胞来源的贴壁细胞可保护 B-CLL 细胞免于凋亡,起到类滋养细胞(NLCs)的作用。氟达拉滨(9-β-D-阿拉伯呋喃糖基-2-氟腺嘌呤;F-ara-A)是一种用于治疗 B-CLL 的腺嘌呤核苷类似物。为深入了解氟达拉滨对 B-CLL 细胞抗肿瘤作用的机制,我们对经氟达拉滨处理和未处理的 B-CLL 细胞与 NLCs 进行了共培养。我们的结果表明,氟达拉滨阻断了 NLCs 的发育,并在共培养时诱导这些细胞凋亡。此外,经氟达拉滨处理的 CD19+/CD5+ B-CLL 细胞发生凋亡,且该事件与 NLCs 是否经氟达拉滨处理无关。总之,氟达拉滨在 CD19+/CD5+ B-CLL 细胞中诱导的凋亡是由于对这些细胞的直接作用,而非对 NLCs 的作用。