Fu S M, Chiorazzi N, Kunkel H G, Halper J P, Harris S R
J Exp Med. 1978 Dec 1;148(6):1570-8. doi: 10.1084/jem.148.6.1570.
Successful induction of in vitro differentiation and immunoglobulin synthesis of the leukemic lymphocytes was carried out in two cases of chronic lymphocytic leukemia. Few plasma cells and little specific Ig secretion were detected in the cultures of isolated leukemic B cells in either the presence or the absence of autologous T cells. Up to 30% of the leukemic B cells matured to plasma cells, and a 32-fold increase in specific Ig synthesis was observed when T cells from normal individuals were added to the cultures of these leukemic B cells. In one of the two cases, autologous T cells were able to induce greater than 50% of the leukemic B cells to differentiate further to plasma cells in the presence of pokeweed mitogen. This markedly accelerated in vitro differentiation was only achieved with leukemic cells from cases in which there was evidence of slight differentiation in vivo. No evidence could be obtained for excessive suppressor T cells in these patients. However, a T-cell defect in the generation of allogeneic effect helper factors was identified. This defect may be responsible for the reduced rate of leukemic maturation in vivo.
在两例慢性淋巴细胞白血病患者中成功实现了白血病淋巴细胞的体外分化诱导及免疫球蛋白合成。在分离的白血病B细胞培养物中,无论有无自体T细胞,均检测到少量浆细胞和少量特异性Ig分泌。当将来自正常个体的T细胞添加到这些白血病B细胞的培养物中时,高达30%的白血病B细胞成熟为浆细胞,且特异性Ig合成增加了32倍。在这两例中的一例中,在有商陆有丝分裂原存在的情况下,自体T细胞能够诱导超过50%的白血病B细胞进一步分化为浆细胞。这种明显加速的体外分化仅在体内有轻微分化证据的病例的白血病细胞中实现。在这些患者中未获得存在过多抑制性T细胞的证据。然而,发现了在同种异体效应辅助因子产生方面的T细胞缺陷。这种缺陷可能是体内白血病成熟率降低的原因。