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:Catheter-Associated Trichosporon japonicum Fungemia in a Patient with Diffuse Large B-Cell Lymphoma Following CAR-T Cell Therapy: A Case Report and Literature Review.
Catheter-Associated Trichosporon japonicum Fungemia in a Patient with Diffuse Large B-Cell Lymphoma Following CAR-T Cell Therapy: A Case Report and Literature Review.
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该病例为关于 T 的有限文献增添了资料。
日本毛孢子菌(Trichosporon japonicum)是一种罕见但致死率很高的病原体,可在免疫功能低下患者中引起真菌血症。随着CAR-T(CAR-T)细胞疗法应用扩大,机会性真菌感染谱正在变化,但该治疗背景下日本毛孢子菌感染的资料仍很有限。 病例介绍:一名69岁弥漫大B细胞淋巴瘤男性患者在CAR-T 细胞再输注后发生导管相关真菌血症。患者最初出现颈痛和口腔黏膜白斑,4天后出现发热。外周血和中心静脉导管尖端培养均分离出日本毛孢子菌,并通过显微镜检查、质谱和分子测序鉴定。在发热前,依据对患者白细胞计数、降钙素原、白细胞介素6和C反应蛋白的密切监测,已开始抗真菌预防;随后根据菌种鉴定和抗真菌药物敏感性结果调整治疗。拔除导管并恢复免疫功能后,感染在2周内得到控制。患者在6个月随访时情况良好。
该病例补充了CAR-T 治疗患者日本毛孢子菌真菌血症的有限文献。我们的经验结合文献回顾提示,成功管理需要及时拔除导管、恢复免疫功能,并联合使用伏立康唑和两性霉素B;应避免单用棘白菌素。提高对免疫功能低下患者中该病原体的认识至关重要。
Trichosporon japonicum is a rare but highly lethal pathogen causing fungemia in immunocompromised patients. With the expanding use of chimeric antigen receptor T (CAR-T) cell therapy, the spectrum of opportunistic fungal infections is changing, yet data on T. japonicum infections in this setting remain scarce. CASE PRESENTATION: A 69-year-old man with diffuse large B-cell lymphoma developed catheter-associated fungemia after CAR-T cell reinfusion. He initially presented with neck pain and white oral mucosal patches, followed by fever four days later. T. japonicum was isolated from both peripheral blood and central venous catheter tip cultures, identified by microscopic examination, mass spectrometry, and molecular sequencing. Antifungal prophylaxis was initiated before fever onset based on close monitoring of white blood cell count, procalcitonin, interleukin-6, and C-reactive protein; treatment was subsequently adjusted according to species identification and antifungal susceptibility results. Infection was controlled within two weeks after catheter removal and immune recovery. The patient remained well at six-month follow-up.
This case adds to the limited literature on T. japonicum fungemia in patients receiving CAR-T therapy. Our experience, together with a review of the literature, underscores that successful management requires prompt catheter removal, immune restoration, and combination therapy with voriconazole and amphotericin B, as echinocandin monotherapy should be avoided. Awareness of this pathogen in immunocompromised patients is critical.
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