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:Successful salvage therapy of ruxolitinib on interstitial pneumonia after long COVID or post-COVID-19 syndrome with follicular lymphoma: two case reports and literature review.
Successful salvage therapy of ruxolitinib on interstitial pneumonia after long COVID or post-COVID-19 syndrome with follicular lymphoma: two case reports and literature review.
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鲁索替尼可能是一种安全有效的替代挽救疗法,适用于有间质炎症和持续性低氧血症、但细胞因子水平不高且对皮质类固醇无反应的 COVID-19 患者。
接受抗CD19嵌合抗原受体(CAR)T细胞治疗的复发/难治性滤泡性淋巴瘤(FL)患者,若出现B淋巴细胞缺乏和低丙种球蛋白血症,属于免疫功能低下人群,发生重症2019冠状病毒病(COVID-19)感染的风险较高。病例描述:在我们的研究中,两例难治性FL患者在接受抗CD19 CAR-T 细胞治疗后出现持续性COVID-19感染。患者被诊断为COVID-19后综合征或伴有间质性炎症和持续性低氧血症的COVID-19。当患者白细胞介素(IL)-6水平较高时,接受了molnupiravir和Paxlovid治疗,并联合甲泼尼龙治疗。间质性炎症、持续性低氧血症或严重急性呼吸综合征冠状病毒2(SARS-CoV-2)持续阳性表达均未观察到缓解;然而,这些治疗后IL-6水平下降。这两例患者随后接受了低剂量ruxolitinib(5 mg,每日两次)作为挽救治疗,并联合逐渐减量的甲泼尼龙。ruxolitinib治疗1-2个月后,持续性低氧血症得到缓解,间质性炎症明显吸收。同时,SARS-CoV-2检测转为阴性。
Immunocompromised patients with B lymphocyte deficiency and hypogammaglobulinemia after anti-CD19 chimeric antigen receptor (CAR) T cell therapy for relapsed/refractory follicular lymphoma (FL) are at high risk of severe coronavirus disease 2019 (COVID-19) infection. CASE DESCRIPTION: In our study, two patients with refractory FL had persistent COVID-19 infection after their anti-CD19 CAR T cell therapy. The patients were diagnosed with post-COVID-19 syndrome or COVID-19 with interstitial inflammation and persistent hypoxemia. The patients received molnupiravir and Paxlovid, along with methylprednisolone therapy when their interleukin (IL)-6 levels were high. No response was observed in interstitial inflammation, persistent hypoxemia, or persistent positive expression of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2); however, the level of IL-6 decreased after these therapies. These two patients subsequently received low-dose ruxolitinib (5 mg, twice daily) as salvage therapy in combination with a gradually reduced dosage of methylprednisolone. After 1-2 months of ruxolitinib therapy, persistent hypoxemia was relieved, and interstitial inflammation was significantly absorbed. At the same time, the SARS-CoV-2 detection was found to be negative.
Ruxolitinib might be a safe and effective alternative salvage therapy for patients with COVID-19 having interstitial inflammation and persistent hypoxemia without high cytokine levels and no response to corticosteroids.
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