Shi Jumei, Tricot Guido, Szmania Susann, Rosen Nancy, Garg Tarun K, Malaviarachchi Priyangi A, Moreno Amberly, Dupont Bo, Hsu Katharine C, Baxter-Lowe Lee Ann, Cottler-Fox Michele, Shaughnessy John D, Barlogie Bart, van Rhee Frits
Myeloma Institute for Research and Therapy, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA.
Br J Haematol. 2008 Dec;143(5):641-53. doi: 10.1111/j.1365-2141.2008.07340.x. Epub 2008 Oct 16.
Killer immunoglobulin-like receptor (KIR)-ligand mismatched natural killer (NK) cells play a key role in achieving durable remission after haplo-identical transplantation for acute myeloid leukaemia. We investigated the feasibility of transfusing haplo-identical, T-cell depleted, KIR-ligand mismatched NK cells, after conditioning therapy with melphalan and fludarabine, to patients with advanced multiple myeloma (MM) followed by delayed rescue with autologous stem cells. No graft-versus-host disease or failure of autologous stem cells to engraft was observed. There was significant variation in the number of allo-reactive NK cells transfused. However, all NK products containing allo-reactive NK cells killed the NK cell target K562, the MM cell line U266, and recipient MM cells when available. Post NK cell infusion there was a rise in endogenous interleukin-15 accompanied by increasing donor chimaerism. Donor chimaerism was eventually lost, which correlated with the emergence of potent host anti-donor responses indicating that the immunosuppressive properties of the conditioning regimen require further optimization. Further, blocking of inhibitory KIR-ligands with anti-human leucocyte antigen antibody substantially enhanced killing of MM cells thus highlighting the potential for modulating NK/MM cell interaction. Encouragingly, 50% of patients achieved (near) complete remission. These data set the stage for future studies of KIR-ligand mismatched NK cell therapy in the autologous setting.
杀伤免疫球蛋白样受体(KIR)配体错配的自然杀伤(NK)细胞在急性髓系白血病单倍体相合移植后实现持久缓解中起关键作用。我们研究了在美法仑和氟达拉滨预处理后,将单倍体相合、T细胞去除、KIR配体错配的NK细胞输注给晚期多发性骨髓瘤(MM)患者,随后进行自体干细胞延迟救援的可行性。未观察到移植物抗宿主病或自体干细胞植入失败。输注的同种异体反应性NK细胞数量存在显著差异。然而,所有含有同种异体反应性NK细胞的NK产品在有条件时均能杀死NK细胞靶标K562、MM细胞系U266和受体MM细胞。NK细胞输注后,内源性白细胞介素-15升高,同时供体嵌合率增加。供体嵌合率最终消失,这与强效宿主抗供体反应的出现相关,表明预处理方案的免疫抑制特性需要进一步优化。此外,用抗人白细胞抗原抗体阻断抑制性KIR配体可显著增强对MM细胞的杀伤作用,从而突出了调节NK/MM细胞相互作用的潜力。令人鼓舞的是,50%的患者实现了(接近)完全缓解。这些数据为未来在自体环境中研究KIR配体错配的NK细胞疗法奠定了基础。