拉丁美洲 CAR-T 治疗的可及性：障碍、缺口与前进路径

Access to CAR-T therapy in Latin America: Barriers, gaps, and pathways forward.

通过 mRNA-LNP 工程化 CLL-1 CAR-NK 细胞以获得强效抗肿瘤活性并逆转急性髓系白血病中 HLA-E 介导的耐药

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。

CAR mRNA 工程化 T 细胞与巨噬细胞在清除 CD19⁺ 白血病细胞中的不同效应功能与协同作用

Distinct effector functions and synergy of CAR mRNA-engineered T cells and macrophages in the clearance of CD19(+) leukemia cells.

我们的研究结果凸显了 CAR-T 细胞优越的肿瘤细胞杀伤能力。

基于 CircRNA 的 CD19 靶向 CAR-NK 疗法用于 B 细胞急性淋巴细胞白血病，采用粗球孢子菌来源的 II 组内含子平台

CircRNA-based CD19-targeted CAR-NK therapy for B-cell acute lymphoblastic Leukemia using a Coccidioides immitis-derived group II intron platform.

BNT162b2 mRNA 疫苗接种影响滤泡性淋巴瘤和慢性淋巴细胞白血病患者的肠道微生物组组成

BNT162b2 mRNA vaccination affects the gut microbiome composition of patients with follicular lymphoma and chronic lymphocytic leukemia.

mRNA 工程化 CD5-CAR-γδT(CD5-) 细胞用于 T 细胞急性淋巴细胞白血病的免疫治疗

mRNA-Engineered CD5-CAR-γδT(CD5-) Cells for the Immunotherapy of T-Cell Acute Lymphoblastic Leukemia.

mRNA BNT162b2 疫苗在五组免疫功能低下患者和健康对照中针对 SARS-CoV-2 的安全性和疗效：一项前瞻性开放标签临床试验

Safety and efficacy of the mRNA BNT162b2 vaccine against SARS-CoV-2 in five groups of immunocompromised patients and healthy controls in a prospective

结果显示，mRNA BNT162b2 疫苗在免疫功能低下患者中是安全的。

泛素特异性蛋白酶 6 mRNA 脂质纳米颗粒在尤文肉瘤中激发抗肿瘤免疫并抑制肿瘤发生

Ubiquitin-Specific Protease 6 mRNA Lipid Nanoparticles Ignite Antitumor Immunity and Suppress Tumorigenesis in Ewing Sarcoma.

经临床批准的 LNP 强制表达 BATF 增强过继 T 细胞治疗

Enforced BATF expression via clinically approved LNPs enhances adoptive T-cell therapies.

mRNA 递送在肿瘤免疫治疗中的应用

Applications of mRNA Delivery in Cancer Immunotherapy.