CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Anaphylaxis During CAR T-Cell Infusion in an HIV-Positive Patient With High-Grade B-Cell Lymphoma: A Case Report and Literature Review.
Anaphylaxis During CAR T-Cell Infusion in an HIV-Positive Patient With High-Grade B-Cell Lymphoma: A Case Report and Literature Review.
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嵌合抗原受体(CAR)T细胞疗法是复发/难治性大B细胞淋巴瘤(LBCL)的高效治疗方法,但由于HIV感染者(PLWH)被排除在关键试验之外,其在该人群中的临床经验仍然有限。
我们报告一例55岁HIV合并高级别B细胞淋巴瘤男性患者,在接受axicabtagene ciloleucel(axi-cel)输注期间发生严重过敏反应,在输注约50%计划剂量后被迫提前终止。该患者仅发生1级细胞因子释放综合征,未出现神经毒性。尽管输注不完整,他在输注后第+30天、+60天和+110天的PET/CT成像上仍达到持续的部分代谢缓解。HIV在整个过程中保持良好控制,未观察到感染性并发症。本病例既凸显了在病毒学抑制的PLWH中实施CAR-T 细胞疗法的可行性,也提示即使部分细胞输注也可能带来临床获益。
此外,它提醒人们关注过敏反应这一罕见但严重的输注相关不良事件。据我们所知,这是首例PLWH对axi-cel发生过敏反应的报告。该病例强调需要加强药物警戒和输注前风险评估。它也支持越来越多的证据,即不应将PLWH一概排除在CAR-T 细胞治疗可及性或临床试验之外。
Chimeric antigen receptor (CAR) T-cell therapy is a highly effective treatment for relapsed or refractory large B-cell lymphoma (LBCL), but clinical experience in people living with HIV (PLWH) remains limited due to their exclusion from pivotal trials.
We report the case of a 55-year-old man with HIV and high-grade B-cell lymphoma who developed severe anaphylaxis during axicabtagene ciloleucel (axi-cel) infusion, requiring early termination after approximately 50% of the planned dose was delivered. The patient experienced only Grade 1 cytokine release syndrome and no neurotoxicity.
Despite incomplete infusion, he achieved a sustained partial metabolic response on PET/CT imaging at Days +30, +60, and +110 post-infusion. HIV remained well-controlled throughout, and no infectious complications were observed. This case highlights both the feasibility of administering CAR T-cell therapy in virologically suppressed PLWH and the potential for clinical benefit even with partial cell delivery.
In addition, it draws attention to anaphylaxis as a rare but serious infusion-related adverse event. To our knowledge, this is the first report of anaphylaxis to axi-cel in a PLWH. The case underscores the need for enhanced pharmacovigilance and pre-infusion risk assessment. It also supports growing evidence that PLWH should not be categorically excluded from CAR T-cell access or clinical trials.
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