分泌抗 CD73 scFv 的增强型 CD33 CAR-NK 细胞克服腺苷介导的免疫抑制并提高抗 AML 疗效
Enhanced CD33 CAR-NK cells secreting anti-CD73scFv overcome adenosine-mediated immunosuppression and improve anti-AML efficacy.
CD33-CD73 双靶向 CAR-NK 平台协同靶向 AML 细胞和富含腺苷的肿瘤微环境,展现出更优的抗白血病疗效。
FRONTIER PAPERS
Enhanced CD33 CAR-NK cells secreting anti-CD73scFv overcome adenosine-mediated immunosuppression and improve anti-AML efficacy.
CD33-CD73 双靶向 CAR-NK 平台协同靶向 AML 细胞和富含腺苷的肿瘤微环境,展现出更优的抗白血病疗效。
Exploring CAR cell therapies beyond CAR-T for myeloid malignancies.
嵌合抗原受体(CAR)-T细胞在多种血液系统恶性肿瘤中已展现出显著疗效;
Progress in reprogramming failed graft-versus-leukemia immunity in acute myeloid leukemia relapse after allogeneic transplantation.
急性髓系白血病(AML)异基因造血干细胞移植(allo-HSCT)后复发影响40-50%的受者,并且仍然是移植后死亡的主要原因;中位总生存期约为5个月,1年生存率低于20%。
Engineering CLL-1 CAR-NK cells via mRNA-LNP for potent antitumor activity and reversal of HLA-E-mediated resistance in acute myeloid leukemia.
瞬时、非整合的 mRNA LNP 转染的 CLL-1 CAR-NK 细胞为 MDR AML 提供了一种安全有效的策略。
Erratum to "CircRNA-based CD19-targeted CAR-NK therapy for B-cell acute lymphoblastic leukemia using a Coccidioides immitis-derived group II intron pl
Pluripotent stem cell-derived CAR-NK progenitor therapy targets minimal residual disease and prevents relapse in leukemia models.
降低化疗后的复发率仍是提高肿瘤治疗疗效的一大挑战。
Donor-derived CD19-targeted CAR-NK cells induce complete remission in a child with relapsed B-ALL after failure of blinatumomab and autologous CD19-ta
复发仍是儿童 B 细胞急性淋巴细胞白血病(B-ALL)治疗失败和死亡的主要原因。
Functional genomics-guided design of CAR-T and CAR-NK therapies in hematological malignancies: aligning cellular engineering with immune escape and mi
一种以耐药为导向的策略可能有助于使工程化细胞疗法的设计与高危血液系统恶性肿瘤中治疗失败的主要机制相一致。未来的 CAR-T 和 CAR-NK 开发不应仅仅增加工程化复杂性,而应将每一处改造与可测量的耐药机制、可行的生物标志物以及可在临床中检验的获益联系起来。在耐药匹配的细胞免疫治疗能够广泛整合进入临床实践之前,前瞻性验证、基因组安全性评估、生产一致性以及长期监测将是必不可少的。
CircRNA-based CD19-targeted CAR-NK therapy for B-cell acute lymphoblastic Leukemia using a Coccidioides immitis-derived group II intron platform.
这些结果支持基于circRNA的CAR-NK疗法作为提高癌症免疫治疗安全性和有效性的一种有效方法的潜力。
Beyond exhaustion: T cell fitness for next generation of immunotherapy for hematological cancer.
T细胞导向的免疫疗法已改变了血液系统恶性肿瘤的治疗,但持久获益仍受限于复发、持续性差、免疫重建不完全和感染。
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