决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
英文原题:Outcomes with chimeric antigen receptor T-cell therapy in Rheumatological disorders: A systematic review.
Outcomes with chimeric antigen receptor T-cell therapy in Rheumatological disorders: A systematic review.
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CAR-T 细胞疗法是风湿性疾病管理中的范式转变,能改善症状并实现这些疾病的生化控制。尽管初步证据显示前景可观的结果,但仍需长期随访和前瞻性临床试验来确定最佳时机,并评估 CAR-T 免疫治疗的安全性和有效性。
CAR-T 细胞疗法是一种新兴的免疫治疗形式,近期在治疗血液恶性肿瘤方面获得认可。CAR-T 疗法的成功应用引起了其在难治性风湿性疾病中应用的兴趣。在此,我们将综述CAR-T 疗法在风湿性疾病中的应用。
根据PRISMA指南,我们在PubMed、Cochrane和ClinicalTrials.gov上使用关键词“CAR-T 细胞疗法”和“风湿性疾病”进行了全面的文献检索,时间范围从建库至2023年12月9日。在筛选了2977篇文章后,有六项研究报告了CAR-T 细胞疗法在患有基础自身免疫/风湿性疾病患者中的结局。我们进行了描述性分析以呈现人口统计学特征和临床结局。
本系统综述共纳入六项研究中的101名成年患者。参与者中位年龄为50.8岁(IQR:14.875),年龄范围从18岁到83岁。纳入的研究包括2篇病例报告、1个病例系列、1项观察性研究和2项临床试验。这些研究在全球范围内开展,包括美国、德国和中国。基础风湿病疾病包括系统性红斑狼疮(17.8%)、类风湿关节炎(23.8%)、重症肌无力(13.8%)、视神经脊髓炎(11.9%)及其他(32.7%)。CAR-T 治疗靶点包括四项研究中的CD-19和两项研究中的B细胞成熟抗原(BCMA)。所有患者均接受过既往治疗,包括糖皮质激素和改善病情抗风湿药。随访时间从1个月到1.5年不等。大多数研究报告了基础疾病症状的改善和血清学生物标志物的下降。纳入研究中的显著结局是六项研究中有五项达到100%的缓解率。五项研究观察到1级和2级细胞因子释放综合征(CRS)。仅一项研究报告了3级或更高级别的CRS。在不良事件中,有2名患者(1.98%)出现神经毒性。
Chimeric antigen receptor T cell (CAR-T) therapy is an emerging form of immunotherapy that has recently gained recognition for treating hematological malignancies. This successful utilization of CAR-T therapy has attracted interest in its application in refractory rheumatological diseases. Here, we will review the use of CAR-T therapy in rheumatological diseases.
Per PRISMA guidelines, a comprehensive literature search was performed on PubMed, Cochrane, and ClinicalTrials.gov using keywords for 'CAR-T cell therapy' and 'Rheumatological diseases' from inception to December 9, 2023. After screening 2977 articles, six studies reporting outcomes of CAR-T cell therapies in patients with underlying autoimmune /rheumatological diseases. Descriptive analysis was performed to represent demographics and clinical outcomes.
A total of 101 adult patients from six studies were included in this systematic review. The median age of the participants was 50.8 years (IQR: 14.875), with ages ranging from 18 to 83 years. The included studies comprised 2 case reports, 1 case series, one observational study, and two clinical trials. The studies were conducted globally, including USA, Germany, and China. The underlying rheumatologic conditions were systemic lupus erythematosus (17.8 %), rheumatoid arthritis (23.8 %), myasthenia gravis (13.8 %), neuromyelitis optica (11.9 %), and others (32.7 %). The target of CAR-T therapy included CD-19 in four studies and B cell maturation antigen (BCMA) in two studies. All the patients were on prior therapy, including glucocorticoids and disease-modifying antirheumatic drugs. Follow-up ranged from a month to 1.5 years. Most of the studies reported improvement in the symptoms and decline in serological biomarkers of the underlying disease. The notable outcomes in the included studies were a 100 % response rate in five out of six studies. Grade 1 and 2 cytokine release syndrome (CRS) was observed in five studies. Only one study reported Grade 3 or higher CRS. 2 patients (1.98 %) developed neurotoxicity among the adverse effects.
CAR-T cell therapy is a paradigm shift in managing rheumatologic diseases, with symptomatic improvement and biochemical control of these diseases. Although preliminary evidence indicates promising results, long-term follow-up and prospective clinical trials are needed to establish optimal timing and assess the safety and efficacy of CAR-T immunotherapy.
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