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.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Management of Clostridioides difficile infection in patients with haematological malignancies and after cellular therapy: guidelines from 10th European Conference on Infections in Leukaemia (ECIL-10).
Management of Clostridioides difficile infection in patients with haematological malignancies and after cellular therapy: guidelines from 10th European Conference on Infections in Leukaemia (ECIL-10).
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。
艰难梭菌感染(CDI)给血液系统恶性肿瘤(HM)患者及接受造血细胞移植(HCT)或 CAR-T 等细胞治疗的患者带来重大挑战。这些患者艰难梭菌定植率较高,且常因非感染性原因腹泻,使 CDI 的确诊和最佳管理较为困难;若仅检测毒素基因,更增加诊断难度。现行严重程度标准的适用性有限,因为基础血液病及其治疗会影响白细胞计数和重症 CDI 的炎症表现。大量抗生素暴露、肠道微生物群严重受损,以及移植后 CDI 与胃肠道移植物抗宿主病之间的双向关系,进一步增加临床管理难度。因此,第 10 届白血病感染欧洲会议(ECIL-10)工作组全面回顾了 2010 年 1 月 1 日至 2024 年 9 月 15 日发表的 CDI 流行病学、治疗和预防文献,并制定针对该人群的 CDI 管理共识建议。工作组还提出了适用于该人群的确诊、很可能及可能 CDI 新定义,以便在临床研究中标准化报告。
Clostridioides difficile infection (CDI) poses a significant challenge in patients with haematological malignancies (HM) and those undergoing cellular therapy such as haematopoietic cell transplantation (HCT) or CAR T-cell therapy. These patients have high rates of both colonization with Clostridioides difficile and diarrhoea due to non-infectious causes, leading to challenges with establishing diagnosis and optimal management of CDI, especially in the setting of molecular detection of toxin genes alone.
Current severity criteria are of limited usefulness since underlying haematological disease and its treatment impact white blood count and inflammatory manifestations of severe CDI. Extensive exposure to antibiotics, profound microbiota damage and bidirectional relationship with gastro-intestinal graft-versus-host disease after transplant further complicate clinical management.
Therefore, the 10th European Conference on Infections in Leukemia (ECIL-10) group comprehensively reviewed the literature (published 01/01/2010-15/09/2024) on the epidemiology, treatment and prevention of CDI, and formulated consensus recommendations for the management of CDI specific to this population. New definitions of proven, probable and possible CDI in this population were developed and proposed for use in clinical research to standardise reporting.
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