Department of Medicine, University of Connecticut Health Center, Farmington, CT 06030, USA.
Clin Immunol. 2010 Sep;136(3):338-47. doi: 10.1016/j.clim.2010.04.013. Epub 2010 May 23.
MHC class I-restricted human melanoma epitope MART-1(27-35) specific TCR-engineered CD4+CD25- T cells synthesize Th1 type cytokines and exhibit cytolytic effector function upon cognate stimulation. A detailed characterization of such TCR-engineered CD4+CD25- T cells now reveals that they are multifunctional. For example, they undergo multiple rounds of division, synthesize cytokines (IFN-gamma, TNF-alpha, IL-2, and MIP1ss), lyse target cells, and "help" the expansion of the MART-1(27-35) specific CD8+ T cells when stimulated by the MART-1(27-35) peptide pulsed DC. Multiparametric analyses reveal that a single TCR-engineered CD4+ T cell can perform as many as five different functions. Nearly 100% MART-1(27-35) specific TCR expressing CD4+ T cells can be generated through retroviral vector-based transduction and one round of in vitro stimulation by the peptide pulsed DC. MHC class I-restricted tumor epitope specific TCR transduced CD4+ T cells, therefore, could be useful in immunotherapeutic strategies for melanoma or other human malignancies.
MHC Ⅰ类限制性人类黑色素瘤抗原 MART-1(27-35)特异性 TCR 工程化 CD4+CD25-T 细胞在识别性刺激下合成 Th1 型细胞因子并发挥细胞毒效应功能。对这些 TCR 工程化 CD4+CD25-T 细胞的详细特征分析表明,它们具有多功能性。例如,它们可以经历多轮分裂,合成细胞因子(IFN-γ、TNF-α、IL-2 和 MIP1ss),裂解靶细胞,并在 MART-1(27-35)肽脉冲 DC 刺激下“帮助”MART-1(27-35)特异性 CD8+T 细胞的扩增。多参数分析表明,单个 TCR 工程化 CD4+T 细胞可以执行多达五种不同的功能。通过逆转录病毒载体转导和一轮肽脉冲 DC 体外刺激,可以产生近 100%表达 MART-1(27-35)特异性 TCR 的 CD4+T 细胞。因此,MHC Ⅰ类限制性肿瘤表位特异性 TCR 转导的 CD4+T 细胞可能在黑色素瘤或其他人类恶性肿瘤的免疫治疗策略中有用。