首页> 外文期刊>BMC Infectious Diseases >Severe Candida glabrata pancolitis and fatal Aspergillus fumigatus pulmonary infection in the setting of bone marrow aplasia after CD19-directed CAR T-cell therapy – a case report
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Severe Candida glabrata pancolitis and fatal Aspergillus fumigatus pulmonary infection in the setting of bone marrow aplasia after CD19-directed CAR T-cell therapy – a case report

机译:严重的Candida Glabrata鼠琼炎和致命的曲霉属Fumigatus肺部感染在CD19针对汽车T细胞疗法后骨髓性肺癌的设置 - 案例报告

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Abstract Background Prolonged myelosuppression following CD19-directed CAR T-cell transfusion represents an important, yet underreported, adverse event. The resulting neutropenia and multifactorial immunosuppression can facilitate severe infectious complications. Case presentation We describe the clinical course of a 59-year-old patient with relapsed/refractory DLBCL who received Axicabtagene-Ciloleucel (Axi-cel). The patient developed ASTCT grade I CRS and grade IV ICANS, necessitating admission to the neurological ICU and prolonged application of high-dose corticosteroids and other immunosuppressive agents. Importantly, neutropenia was profound (ANC ?100/μl), G-CSF-refractory, and prolonged, lasting more than 50?days. The patient developed severe septic shock 3 weeks after CAR transfusion while receiving anti-fungal prophylaxis with micafungin. His clinical status stabilized with broad anti-infective treatment and intensive supportive measures. An autologous stem cell backup was employed on day 46 to support hematopoietic recovery. Although the counts of the patient eventually started to recover, he developed an invasive pulmonary aspergillosis, which ultimately lead to respiratory failure and death. Postmortem examination revealed signs of Candida glabrata pancolitis. Conclusions This case highlights the increased risk for fatal infectious complications in patients who present with profound and prolonged cytopenia after CAR T-cell therapy. We describe a rare case of C. glabrata pancolitis associated with multifactorial immunosuppression. Although our patient succumbed to a fatal fungal infection, autologous stem cell boost was able to spur hematopoiesis and may represent an important therapeutic strategy for DLBCL patients with CAR T-cell associated bone marrow aplasia who have underwent prior stem cell harvest.
机译:摘要背景延长了CD19导向的汽车T细胞输血后延长髓抑制代表了一个重要但低估的不良事件。所得到的中性粒细胞减少和多学会免疫抑制可以促进严重的传染性并发​​症。案例介绍我们描述了一个59岁患者的临床过程,其中接受了Axicabtagene-Ciloleucel(Axi-Cel)的复发/难治性DLBCL。患者开发了ASTCT等级CRS和IV级ICAN,需要进入神经系统ICU和高剂量皮质类固醇和其他免疫抑制剂的长期应用。重要的是,中性粒细胞病原体(ANC&?100 /μl),g-csf-ructory和延长,持续超过50℃。患者在汽车输血后3周发育严重的化粪池休克,同时接受Micafungin的抗真菌预防。他的临床状态稳定,具有广泛的抗感染性治疗和强化支持措施。在第46天使用自体干细胞备用,以支持造血回收。虽然患者的计数最终开始恢复,但他开发了一种侵袭性肺曲线,最终导致呼吸衰竭和死亡。后期检查揭示了念珠菌毒菌炎的迹象。结论这种情况突出了在汽车T细胞治疗后患有深刻和长期细胞缺乏的患者致命传染性并发​​症的风险增加。我们描述了与多因素免疫抑制相关的罕见C.Glabrata致鼠畸形。虽然我们的病人持续到致命的真菌感染,但是自体干细胞增强能够刺激血液缺血,并且可以代表患有患有现有干细胞收获的汽车T细胞相关骨髓Alasia的DLBCL患者的重要治疗策略。

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