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:Prolonged COVID-19 infection in a patient with B-cell acute lymphoblastic leukemia maintained on convalescent plasma until recovery with monoclonal antibodies.
Prolonged COVID-19 infection in a patient with B-cell acute lymphoblastic leukemia maintained on convalescent plasma until recovery with monoclonal antibodies.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
本病例说明了 CCP 在 SARS-CoV-2 长期感染患者中的局限性,并凸显了 mAbs 在重度免疫抑制宿主中实现病毒清除的有效性。它支持在特定高风险人群中靶向使用 mAb 治疗,并强化了在免疫缺陷患者病毒血症管理中采用特异性被动免疫策略(当可用时)的重要性。
接受CAR-T 细胞等免疫抑制治疗的血液系统恶性肿瘤患者,由于体液免疫受损,发生SARS-CoV-2持续感染的风险较高。在此类情况下,治疗选择仍然有限,且疗效不一。
我们描述了一名21岁患有唐氏综合征和B细胞急性淋巴细胞白血病的男性,在接受CD19靶向CAR-T 治疗后并发B细胞发育不全。该患者感染了COVID-19,并经历了持续的症状性感染,病毒载量高,逆转录聚合酶链反应(RT-PCR)阳性持续超过7个月。
尽管使用了多疗程的瑞德西韦和延长每周输注的COVID-19恢复期血浆(CCP),患者仍持续存在病毒血症并间歇性出现症状。抗SARS-CoV-2免疫球蛋白G滴度仅在治疗后期可检测到,使用CCP的被动抗体治疗不足以清除病毒。最终,获准同情使用单克隆抗体(mAb)治疗(casirivimab和imdevimab)。给药后,患者首次实现病毒清除,症状消退,并在随后8个月的可用随访中持续保持RT-PCR阴性。
We describe a 21-year-old man with Down syndrome and B-cell acute lymphoblastic leukemia complicated by B-cell aplasia following CD19-directed CAR-T therapy. The patient developed COVID-19 and experienced persistent symptomatic infection, with high viral load and prolonged reverse transcriptase-polymerase chain reaction (RT-PCR) positivity for more than 7 months.
Despite multiple courses of remdesivir and extended weekly infusions of COVID-19 convalescent plasma (CCP), the patient remained viremic and intermittently symptomatic. Anti-SARS-CoV-2 immunoglobulin G titers were detectable only toward the latter time frame of treatment, and passive antibody therapy with CCP was insufficient for viral clearance. Ultimately, compassionate use of monoclonal antibody (mAb) therapy (casirivimab and imdevimab) was granted. Following administration, the patient achieved viral clearance for the first time, with resolution of symptoms and persistently negative RT-PCR findings for 8 months of available follow-up thereafter. DISCUSSION: This case illustrates the limitations of CCP in patients with prolonged SARS-CoV-2 infection and highlights the effectiveness of mAbs in achieving viral clearance in severely immunocompromised hosts. It supports targeted use of mAb therapy in select high-risk populations and reinforces the importance of specific passive immunotherapy strategies (when available) for the management of viremia in immunodeficient patients.
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