Wilhelm Martin, Kunzmann Volker, Eckstein Susanne, Reimer Peter, Weissinger Florian, Ruediger Thomas, Tony Hans-Peter
Medizinische Poliklinik Wuerzburg, Julius-Maximilians University Wuerzburg, Klinikstrasse 6-8, 97070 Wuerzburg, Germany.
Blood. 2003 Jul 1;102(1):200-6. doi: 10.1182/blood-2002-12-3665. Epub 2003 Mar 6.
There is increasing evidence that gammadelta T cells have potent innate antitumor activity. We described previously that synthetic aminobisphosphonates are potent gammadelta T cell stimulatory compounds that induce cytokine secretion (ie, interferon gamma [IFN-gamma]) and cell-mediated cytotoxicity against lymphoma and myeloma cell lines in vitro. To evaluate the antitumor activity of gammadelta T cells in vivo, we initiated a pilot study of low-dose interleukin 2 (IL-2) in combination with pamidronate in 19 patients with relapsed/refractory low-grade non-Hodgkin lymphoma (NHL) or multiple myeloma (MM). The objectives of this trial were to determine toxicity, the most effective dose for in vivo activation/proliferation of gammadelta T cells, and antilymphoma efficacy of the combination of pamidronate and IL-2. The first 10 patients (cohort A) who entered the study received 90 mg pamidronate intravenously on day 1 followed by increasing dose levels of continuous 24-hour intravenous (IV) infusions of IL-2 (0.25 to 3 x 106 IU/m2) from day 3 to day 8. Even at the highest IL-2 dose level in vivo, gammadelta T-cell activation/proliferation and response to treatment were disappointing with only 1 patient achieving stable disease. Therefore, the next 9 patients were selected by positive in vitro proliferation of gammadelta T cells in response to pamidronate/IL-2 and received a modified treatment schedule (6-hour bolus IV IL-2 infusions from day 1-6). In this patient group (cohort B), significant in vivo activation/proliferation of gammadelta T cells was observed in 5 patients (55%), and objective responses (PR) were achieved in 3 patients (33%). Only patients with significant in vivo proliferation of gammadelta T cells responded to treatment, indicating that gammadelta T cells might contribute to this antilymphoma effect. Overall, administration of pamidronate and low-dose IL-2 was well tolerated. In conclusion, this clinical trial demonstrates, for the first time, that gammadelta T-cell-mediated immunotherapy is feasible and can induce objective tumor responses.
越来越多的证据表明,γδ T细胞具有强大的先天性抗肿瘤活性。我们之前描述过,合成氨基双膦酸盐是有效的γδ T细胞刺激化合物,可在体外诱导细胞因子分泌(即干扰素γ [IFN-γ])以及对淋巴瘤和骨髓瘤细胞系的细胞介导的细胞毒性。为了评估γδ T细胞在体内的抗肿瘤活性,我们对19例复发/难治性低度非霍奇金淋巴瘤(NHL)或多发性骨髓瘤(MM)患者开展了一项低剂量白细胞介素2(IL-2)联合帕米膦酸盐的初步研究。该试验的目的是确定毒性、γδ T细胞在体内激活/增殖的最有效剂量以及帕米膦酸盐和IL-2联合治疗的抗淋巴瘤疗效。入组的前10例患者(A组)在第1天静脉注射90 mg帕米膦酸盐,随后从第3天至第8天给予递增剂量水平的连续24小时静脉(IV)输注IL-2(0.25至3×106 IU/m2)。即使在体内最高IL-2剂量水平下,γδ T细胞的激活/增殖及对治疗的反应也令人失望,只有1例患者病情稳定。因此,接下来的9例患者根据γδ T细胞对帕米膦酸盐/IL-2的体外增殖阳性进行选择,并接受了改良治疗方案(第1 - 6天静脉推注6小时IL-2)。在该患者组(B组)中,5例患者(55%)观察到γδ T细胞在体内显著激活/增殖,3例患者(33%)达到客观缓解(PR)。只有γδ T细胞在体内显著增殖的患者对治疗有反应,表明γδ T细胞可能促成了这种抗淋巴瘤效应。总体而言,帕米膦酸盐和低剂量IL-2的给药耐受性良好。总之,这项临床试验首次证明,γδ T细胞介导的免疫疗法是可行的,并且可以诱导客观的肿瘤反应。