Söderberg O, Christiansen I, Nilsson G, Carlsson M, Nilsson K
Department of Pathology, University of Uppsala, University Hospital, Sweden.
Leukemia. 1997 Aug;11(8):1298-304. doi: 10.1038/sj.leu.2400728.
We have previously shown that Staphylococcus aureus Cowan strain 1 particles (SAC) + thioredoxin (Trx) + IL-2 may induce B-chronic lymphocytic leukemia (B-CLL) cells to proliferate. In this paper we have examined IL-15, which has activities similar to IL-2, for its ability to stimulate B-CLL cells and compared its activity with that of IL-2. We found that B-CLL cells could be induced to DNA synthesis upon treatment with IL-15 + Trx. The presence of Trx was essential for the IL-15-induced DNA synthesis. This contrasts to the effect of IL-15 + Trx on normal CD5+ and CD5- B cells, where IL-15 + Trx alone only induced limited DNA synthesis. IL-15 was as effective in the induction of DNA synthesis in B-CLL cells as IL-2, but about 100-fold less potent with an EC50 of 200 ng/ml. In addition we found that the IL-15 + Trx-induced proliferation was inhibited by CD40 stimulation. We conclude that IL-15 together with a proper costimulus can induce B-CLL cells to proliferate in vitro.
我们之前已经表明,金黄色葡萄球菌考恩1株颗粒(SAC)+硫氧还蛋白(Trx)+白细胞介素-2(IL-2)可能诱导B细胞慢性淋巴细胞白血病(B-CLL)细胞增殖。在本文中,我们研究了具有与IL-2相似活性的IL-15刺激B-CLL细胞的能力,并将其活性与IL-2的活性进行了比较。我们发现,用IL-15+Trx处理后,B-CLL细胞可被诱导进行DNA合成。Trx的存在对于IL-15诱导的DNA合成至关重要。这与IL-15+Trx对正常CD5+和CD5- B细胞的作用形成对比,在正常细胞中,单独的IL-15+Trx仅诱导有限的DNA合成。IL-15在诱导B-CLL细胞DNA合成方面与IL-2一样有效,但效力约低100倍,半数有效浓度(EC50)为200 ng/ml。此外,我们发现CD40刺激可抑制IL-15+Trx诱导的增殖。我们得出结论,IL-15与适当的共刺激因子一起可在体外诱导B-CLL细胞增殖。