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:Schizophyllum commune infection following chimeric antigen receptor T-cell therapy in a patient with lymphoma.
Schizophyllum commune infection following chimeric antigen receptor T-cell therapy in a patient with lymphoma.
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B细胞淋巴瘤患者接受嵌合抗原受体(CAR)T细胞治疗后,因长期免疫抑制,感染并发症较常见。裂褶菌(Schizophyllum commune)是一种极罕见真菌病原体,通常累及呼吸道,可能类似慢性肺曲霉病。既往裂褶菌感染主要见于异基因造血干细胞移植受者。本文报告首例已知的CAR-T 治疗后裂褶菌感染。一名71岁原发难治性大B细胞淋巴瘤女性患者接受利基仑赛作为二线治疗。治疗后6个月,CT显示右中叶肺不张并伴高密度黏液。支气管镜活检、真菌培养和内转录间隔区测序证实裂褶菌感染,表现为变应性支气管肺真菌病(ABPM)。
值得注意的是,针对真菌特异性免疫球蛋白G和E的血清学检测均为阴性。患者接受4个月口服伏立康唑后反应良好,症状和影像学表现均消退。本病例提示,CAR-T 治疗后可能发生裂褶菌等罕见真菌感染。尽管临床和影像学表现符合ABPM,但缺乏血清学标志物,凸显B细胞靶向免疫治疗所致B细胞缺失带来的诊断挑战。
Infectious complications are common following chimeric antigen receptor (CAR) T-cell therapy for B-cell lymphoma due to its prolonged immunosuppressive effects. Schizophyllum commune is an exceedingly rare fungal pathogen that typically affects the respiratory tract and may mimic chronic pulmonary aspergillosis. Infections caused by S. commune have been primarily reported in recipients of allogeneic hematopoietic stem cell transplantation.
Here, we report the first known case of S. commune infection in a patient treated with CAR T-cell therapy. A 71-year-old woman with primary refractory large B-cell lymphoma received lisocabtagene maraleucel as second-line therapy. Six months post-treatment, computed tomography revealed right middle lobe atelectasis with high-attenuation mucus. Bronchoscopic biopsy, fungal culture, and internal transcribed spacer gene region sequencing confirmed the diagnosis of S. commune infection presenting as allergic bronchopulmonary mycosis (ABPM).
Notably, serologic tests were negative for fungus-specific specific immunoglobulin G and immunoglobulin E. The patient responded favorably to 4 months of oral voriconazole therapy, with resolution of symptoms and radiologic findings. This case highlights the potential for rare fungal infections, such as S.
commune, to occur following CAR T-cell therapy. Although the clinical and radiologic features were consistent with ABPM, the absence of serologic markers underscores the diagnostic challenges posed by B-cell aplasia resulting from B-cell-directed immunotherapy.
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