Golay Josée, D'Amico Anna, Borleri Gianmaria, Bonzi Michela, Valgardsdottir Rut, Alzani Rachele, Cribioli Sabrina, Albanese Clara, Pesenti Enrico, Finazzi Maria Chiara, Quaresmini Giulia, Nagorsen Dirk, Introna Martino, Rambaldi Alessandro
Centro di Terapia Cellulare, "G. Lanzani," USC Ematologia, Azienda Ospedaliera Papa Giovanni XXIII, 24127 Bergamo, Italy;
Centro Trapianto Midollo Osseo, USC Ematologia, Azienda Ospedaliera Papa Giovanni XXIII, 24127 Bergamo, Italy;
J Immunol. 2014 Nov 1;193(9):4739-47. doi: 10.4049/jimmunol.1401550. Epub 2014 Sep 29.
Current treatment of chronic lymphocytic leukemia (CLL) patients often results in life-threatening immunosuppression. Furthermore, CLL is still an incurable disease due to the persistence of residual leukemic cells. These patients may therefore benefit from immunotherapy approaches aimed at immunoreconstitution and/or the elimination of residual disease following chemotherapy. For these purposes, we designed a simple GMP-compliant protocol for ex vivo expansion of normal T cells from CLL patients' peripheral blood for adoptive therapy, using bispecific Ab blinatumomab (CD3 × CD19), acting both as T cell stimulator and CLL depletion agent, and human rIL-2. Starting from only 10 ml CLL peripheral blood, a mean 515 × 10(6) CD3(+) T cells were expanded in 3 wk. The resulting blinatumomab-expanded T cells (BET) were polyclonal CD4(+) and CD8(+) and mostly effector and central memory cells. The Th1 subset was slightly prevalent over Th2, whereas Th17 and T regulatory cells were <1%. CMV-specific clones were detected in equivalent proportion before and after expansion. Interestingly, BET cells had normalized expression of the synapse inhibitors CD272 and CD279 compared with starting T cells and were cytotoxic against CD19(+) targets in presence of blinatumomab in vitro. In support of their functional capacity, we observed that BET, in combination with blinatumomab, had significant therapeutic activity in a systemic human diffuse large B lymphoma model in NOD-SCID mice. We propose BET as a therapeutic tool for immunoreconstitution of heavily immunosuppressed CLL patients and, in combination with bispecific Ab, as antitumor immunotherapy.
慢性淋巴细胞白血病(CLL)患者目前的治疗方法常常导致危及生命的免疫抑制。此外,由于残留白血病细胞的持续存在,CLL仍然是一种无法治愈的疾病。因此,这些患者可能受益于旨在免疫重建和/或化疗后消除残留疾病的免疫治疗方法。出于这些目的,我们设计了一种简单的符合GMP标准的方案,用于从CLL患者外周血中体外扩增正常T细胞以进行过继性治疗,使用双特异性抗体blinatumomab(CD3×CD19),其兼具T细胞刺激剂和CLL清除剂的作用,以及人重组白细胞介素-2。仅从10毫升CLL外周血开始,在3周内平均扩增出515×10⁶个CD3⁺T细胞。由此产生的blinatumomab扩增T细胞(BET)是多克隆的CD4⁺和CD8⁺细胞,且大多为效应细胞和中枢记忆细胞。Th1亚群略多于Th2亚群,而Th17和调节性T细胞<1%。扩增前后检测到的巨细胞病毒特异性克隆比例相当。有趣的是,与起始T细胞相比,BET细胞突触抑制剂CD272和CD279的表达已正常化,并且在体外存在blinatumomab的情况下对CD19⁺靶标具有细胞毒性。为支持其功能能力,我们观察到BET与blinatumomab联合使用时,在NOD-SCID小鼠的全身性人弥漫性大B淋巴瘤模型中具有显著的治疗活性。我们提议将BET作为重度免疫抑制CLL患者免疫重建的治疗工具,并与双特异性抗体联合用作抗肿瘤免疫治疗。