Division of Translational Vaccine Research.
Leuk Lymphoma. 2013 Nov;54(11):2490-9. doi: 10.3109/10428194.2013.783910. Epub 2013 Apr 30.
Wilms' tumor antigen (WT1) is overexpressed in many different solid tumors and hematologic malignancies. However, little is known about WT1 expression or WT1-specific immune responses in patients with non-Hodgkin lymphoma (NHL). In a cross-sectional survey study, we investigated the immune recognition of WT1 by patients with NHL. Utilizing a WT1 overlapping peptide library, we discovered that a large percentage of patients with NHL of all grades maintain WT1-specific T cells. Ex vivo frequencies of these T cells measured from unfractionated samples by the CD137 activation marker assay were high in many patients (some > 1% CD8+). Using standard in vitro techniques we discovered that they were cytotoxic to WT1 peptide library-loaded T2 cells and WT1 antigen-primed autologous Epstein-Barr virus-transformed B cell lines (EBV-LCLs) and expressed interferon gamma (IFN-γ). In addition, we detected WT1 mRNA transcripts in diseased lymph node tissues of patients with NHL utilizing real-time quantitative polymerase chain reaction (RT-qPCR) technology. These results are the first example of strong T cell reactivity against WT1 in patients with NHL which also demonstrate strong cytotoxicity against peptide-loaded tumor cells. The potential for developing WT1 as a target for immunotherapy in NHL deserves further exploration.
Wilms 瘤抗原(WT1)在许多不同的实体瘤和血液恶性肿瘤中过度表达。然而,对于非霍奇金淋巴瘤(NHL)患者的 WT1 表达或 WT1 特异性免疫反应知之甚少。在一项横断面调查研究中,我们研究了 NHL 患者对 WT1 的免疫识别。利用 WT1 重叠肽文库,我们发现所有分级的 NHL 患者中有很大比例保持 WT1 特异性 T 细胞。通过 CD137 激活标志物测定法从未分馏样本中测量这些 T 细胞的体外频率在许多患者中很高(一些> 1% CD8+)。使用标准的体外技术,我们发现它们对 WT1 肽文库加载的 T2 细胞和 WT1 抗原致敏的自身 EBV 转化 B 细胞系(EBV-LCL)具有细胞毒性,并表达干扰素γ(IFN-γ)。此外,我们利用实时定量聚合酶链反应(RT-qPCR)技术在 NHL 患者的病变淋巴结组织中检测到 WT1 mRNA 转录本。这些结果是 NHL 患者对 WT1 产生强烈 T 细胞反应的首例实例,也证明了对肽加载肿瘤细胞的强烈细胞毒性。将 WT1 作为 NHL 免疫治疗的靶标具有进一步探索的潜力。