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:Detection of HIV RNA after CAR-T Cell Therapy in A Relapsed/refractory Diffuse Large B-cell Lymphoma Patient: Possibility of False Positivity and Clinical Implications.
使用慢病毒载体的CAR-T细胞治疗可能导致HIV RNA假阳性检测,使得区分真感染与载体相关信号具有挑战性。
使用慢病毒载体的CAR-T细胞治疗可能导致HIV RNA假阳性检测,使得区分真实感染与载体相关信号具有挑战性。一名64岁男性复发/难治性DLBCL(RR-DLBCL)患者接受了多线治疗,包括R-CHOP、R-ICE、自体干细胞移植(ASCT)和tisagenlecleucel(tisa-cel,Kymriah)。CAR-T治疗前的感染病筛查HIV阴性。然而,输注后四个月,在评估靶向CD20的二线CAR-T治疗时,Roche Cobas HIV-1检测(双靶标:5'LTR和gag基因)检出HIV RNA(48 copies/mL)。连续检测显示HIV RNA持续但低水平阳性。对储存血清样本的回顾性分析显示,tisa-cel输注前HIV RNA阴性,但输注后在Roche Cobas HIV-1检测中呈阳性。使用Alinity m HIV-1检测(双靶标:5'LTR和pol基因)和Abbott RealTime HIV-1检测(单靶标:pol基因)进行的额外检测证实,仅双靶标检测产生阳性结果,提示慢病毒载体交叉反应而非实际HIV感染。本病例强调了CAR-T细胞治疗接受者中因载体衍生序列导致HIV-1 RNA假阳性检测的可能性,强调了对HIV-1检测结果谨慎解读的必要性。
CAR-T cell therapy using lentiviral vectors can lead to false-positive HIV RNA detection, making distinguishing true infection from vector-related signals challenging. A 64-year-old male with relapsed/refractory DLBCL (RR-DLBCL) underwent multiple lines of treatment, including R-CHOP, R-ICE, autologous stem cell transplantation (ASCT), and tisagenlecleucel (tisa-cel, Kymriah). Infectious disease screening before CAR-T therapy was negative for HIV. However, four months post-infusion, during evaluation for second-line CAR-T therapy targeted CD20, HIV RNA was detected in Roche Cobas HIV-1 assay targeted dual target, 5'LTR and gag gene (48 copies/mL). Serial testing showed persistent but low-level positivity of HIV RNA. Retrospective analysis of stored serum samples revealed HIV RNA negativity before tisa-cel infusion but positivity post-infusion in Roche Cobas HIV-1 assay. Additional testing using the Alinity m HIV-1 assay (dual target: 5'LTR and pol gene) and the Abbott RealTime HIV-1 assay (single-target: pol gene) confirmed that only the dual-target assay yielded positive results, suggesting lentiviral vector cross-reactivity rather than actual HIV infection. This case underscores the potential for false-positive HIV-1 RNA detection in CAR-T cell treatment recipients due to vector-derived sequences, emphasizing the need for cautious interpretation of HIV-1 testing.
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