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.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Lymphoma risk in autoimmune diseases with multiple medication use: analysis from the LIFE Study.
Lymphoma risk in autoimmune diseases with multiple medication use: analysis from the LIFE Study.
重要的是,在AID病例中,使用两种或更多药物显著增加了淋巴瘤风险(HR 2.7)。
自身免疫性疾病(AIDs)与淋巴瘤风险增加相关。尽管AIDs的治疗策略已发生实质性变化,但关于这一关联的最新证据仍然缺乏。特别是,新型免疫抑制/免疫调节剂的影响以及多种药物累积使用对淋巴瘤风险的影响尚未得到充分研究。为解决这些问题,我们使用了LIFE研究数据库,该数据库包含日本15个市町村2014年至2023年的医疗索赔数据。在2,229,423人中,211,592人患有AIDs,其中530人随后发展为淋巴瘤。总体而言,AID病例的淋巴瘤发病率显著高于非AID病例(风险比[HR] 1.9)。在23种AIDs中,14种疾病的淋巴瘤风险显著升高,包括高安动脉炎(6.6)和成人斯蒂尔病(4.7)。在免疫抑制/免疫调节剂中,钙调磷酸酶抑制剂、艾拉莫德或甲氨蝶呤与较高的淋巴瘤风险相关。重要的是,在AID病例中,使用两种或以上药物强烈增加了淋巴瘤风险(HR 2.7)。淋巴瘤亚型特异性分析揭示了新的关联,包括系统性红斑狼疮中的T/NK细胞淋巴瘤。我们的大规模队列研究揭示了AID患者淋巴瘤风险增加,尤其是那些接受多种免疫抑制剂/免疫调节剂的患者,强调了对这些患者进行仔细监测的必要性。
Autoimmune diseases (AIDs) are associated with an increased risk of lymphoma. Although treatment strategies have changed substantially in AIDs, recent evidence regarding this association is lacking. Particularly, the impact of novel immunosuppressive/immunomodulatory agents and the cumulative effect of multiple medication use on lymphoma risk have not been well investigated. To address these, we used the LIFE Study database, which contains health care claims data from 2014 to 2023 in 15 municipalities in Japan. Of 2,229,423 individuals, 211,592 had AIDs and 530 subsequently developed lymphoma. Overall, AID cases had a significantly higher incidence of lymphoma than non-AID cases (hazard ratio [HR] 1.9). Among 23 AIDs, lymphoma risk was significantly elevated in 14, including Takayasu arteritis (6.6) and adult-onset Still's disease (4.7). Among immunosuppressive/immunomodulatory agents, calcineurin inhibitors, iguratimod, or methotrexate were associated with higher lymphoma risks. Importantly, the use of two or more medications strongly increased lymphoma risk (HR 2.7) in AID cases. Lymphoma subtype-specific analysis revealed novel associations, including T/NK-cell lymphoma in systemic lupus erythematosus. Our large-scale cohort study reveals an increased risk of lymphoma in AID patients, particularly those receiving multiple immunosuppressants/immunomodulators, underscoring the need for careful monitoring in these patients.
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