决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Near-Infrared Bioluminescence Imaging of Macrophage Sensors for Cancer Detection In Vivo.
黑色素瘤是一种侵袭性皮肤癌,一旦发生转移,预后较差。
黑色素瘤是一种侵袭性皮肤癌,转移后预后较差。恶性黑色素瘤的早期发现对于有效治疗至关重要。由于黑色素瘤常与痣相似,常规皮肤检查可能有助于及时识别可疑区域。近年来,研究表明黑色素瘤细胞与免疫系统的相互作用有助于开发有效的治疗策略。在此,我们利用工程化巨噬细胞(BMC2)作为转移性黑色素瘤的细胞传感器。为了在体内进行双色生物发光成像(BLI),巨噬细胞被工程化以表达绿色点击甲虫荧光素酶(CBG2)和近红外荧光染料(DiR),而B16F10黑色素瘤细胞则被工程化以表达近红外点击甲虫荧光素酶(CBR2)。利用实时体内双色BLI和近红外荧光(FL)成像,我们能够证明巨噬细胞在全身注射后72小时能够感知并大量积聚在皮下和转移性黑色素瘤组织中。总之,我们展示了利用光学成像技术追踪循环巨噬细胞以非侵入性检测转移性黑色素瘤的潜力。
Melanoma is an aggressive type of skin cancer with a poor prognosis after it gets metastasized. The early detection of malignant melanoma is critical for effective therapy. Because melanoma often resembles moles, routine skin check-up may help for timely identification of suspicious areas. Recently, it has been shown that the interplay of melanoma cells with the immune system can help develop efficient therapeutic strategies. Here, we leveraged engineered macrophages (BMC2) as cell-based sensors for metastatic melanoma. To perform dual-color bioluminescence imaging (BLI) in vivo , macrophages were engineered to express a green click beetle luciferase (CBG2) and a near-infrared fluorescent dye (DiR), and B16F10 melanoma cells were instead engineered to express a near-infrared click beetle luciferase (CBR2). Using real-time in vivo dual-color BLI and near-infrared fluorescence (FL) imaging, we could demonstrate that macrophages were able to sense and substantially accumulate in subcutaneous and metastatic melanoma tissues at 72 h after systemic injections. Together, we showed the potentiality to use optical imaging technologies to track circulating macrophages for the non-invasive detection of metastatic melanoma.
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