自体细胞基因治疗中有意为之的异质性:首次人体试验的策略考量
Intentional heterogeneity in autologous cell-based gene therapies: strategic considerations for first-in-human trials.
基于细胞的基因疗法,包括CAR-T、TCR-T和TIL疗法,已经改变了某些癌症的治疗格局,但其在实体瘤中的疗效仍然有限。
FRONTIER PAPERS
Intentional heterogeneity in autologous cell-based gene therapies: strategic considerations for first-in-human trials.
基于细胞的基因疗法,包括CAR-T、TCR-T和TIL疗法,已经改变了某些癌症的治疗格局,但其在实体瘤中的疗效仍然有限。
Engineered T cell therapy for viral and non-viral epithelial cancers.
工程化T细胞疗法在血液系统恶性肿瘤中显示出显著疗效,并具有应用于常见上皮癌的潜力。
Characteristics and developmental trajectory of clinical trials focused on tumor-infiltrating lymphocytes for cancer treatment.
TIL(肿瘤浸润淋巴细胞)在癌症免疫治疗中显示出前景,但其临床应用和发展轨迹仍缺乏充分表征。
Oncolytic virus encoding 4-1BBL and IL15 enhances the efficacy of tumor-infiltrating lymphocyte adoptive therapy in HCC.
既往研究发现,溶瘤病毒(OVs)可提高 TIL 过继疗法在口腔癌、结肠癌和胰腺癌中的疗效。
Improving the cytotoxic response of tumor-infiltrating lymphocytes towards advanced stage ovarian cancer with an oncolytic adenovirus expressing a hum
我们的结果表明,Ad5/3-E2F-d24-vIL2 疗法持续提高了 TILs 疗法在受治的人卵巢癌肿瘤中的细胞毒性。
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