嵌合抗原受体
嗜酸性粒细胞
医学
淋巴瘤
CD8型
免疫学
T细胞
抗原
胃肠病学
内科学
免疫系统
哮喘
作者
Xiuyong Dang,Shiguang Ye,Lili Zhou,Yan Lu,Ping Li,Aibin Liang,Wenbin Qian
出处
期刊:Cytotherapy
[Elsevier]
日期:2022-11-28
卷期号:25 (6): 573-577
标识
DOI:10.1016/j.jcyt.2022.10.010
摘要
Chimeric antigen receptor (CAR) T-cell therapy is a breakthrough treatment for patients with relapsed or refractory diffuse large B-cell lymphoma. However, many patients do not achieve remission or relapse after remission. Previous studies have demonstrated that eosinophils have synergistic anti-tumor effects with CD8+T cells and pre-CAR T-eosinophil counts are associated with the efficacy of CAR T cells.We retrospectively analyzed the eosinophil counts of patients with diffuse large B-cell lymphoma and found it changed remarkably pre- and post-CAR T-cell therapy.Patients who achieved complete remission after CAR T-cell infusion had greater post-CAR T-eosinophil counts than those who did not. Kaplan-Meier curves showed that patients with greater eosinophil counts during the second month after CAR T-cell infusion had superior progression-free survival and overall survival compared with those with lower eosinophil counts.For patients who responded to CAR T-cell therapy, eosinophil counts also can be used to predict 6-month duration of response. In conclusion, the post-CAR T-eosinophil count is associated with the prognosis of patients treated with CAR T-cell therapy and can be used to clinically identify patients who can achieve longer remission after CAR T-cell infusion.
科研通智能强力驱动
Strongly Powered by AbleSci AI