Stauss Hans J
UNIVERSITY COLLEGE LONDON.
Blood. 2017 Mar 9;129(10):1236-1237. doi: 10.1182/blood-2017-01-761510.
In this issue of , Jahn and colleagues have demonstrated that T-cell receptor (TCR) gene transfer can produce cytotoxic T cells that are capable of eliminating myeloma cells in vivo. The therapeutic TCR can equip human T cells with specificity for octamer binding protein-1 (BOB1), a transcription coactivator that is expressed in normal B cells, multiple myeloma, and B-lineage malignancies, thus providing novel options for immunotherapy of B-cell tumors that do not express CD19 or other surface antigens suitable for targeting with chimeric antigen receptor (CAR)–engineered T cells (see figure).
在本期《 》中,扬和同事们证明,T细胞受体(TCR)基因转移可产生能够在体内消除骨髓瘤细胞的细胞毒性T细胞。治疗性TCR可使人类T细胞对八聚体结合蛋白-1(BOB1)具有特异性,BOB1是一种转录共激活因子,在正常B细胞、多发性骨髓瘤和B系恶性肿瘤中表达,从而为不表达CD19或其他适合嵌合抗原受体(CAR)工程化T细胞靶向的表面抗原的B细胞肿瘤免疫治疗提供了新的选择(见图)。