免疫性血小板减少症的新兴治疗进展:2025 ASH 年会精选早期与关键性试验亮点
Emerging therapeutic advances for immune thrombocytopenia: highlights from selected early‑phase and pivotal trials at the 2025 ASH annual meeting.
本通讯重点介绍了 2025 ASH 年会上报告的免疫性血小板减少症 (ITP) 新兴免疫靶向疗法。
FRONTIER PAPERS
Emerging therapeutic advances for immune thrombocytopenia: highlights from selected early‑phase and pivotal trials at the 2025 ASH annual meeting.
本通讯重点介绍了 2025 ASH 年会上报告的免疫性血小板减少症 (ITP) 新兴免疫靶向疗法。
CAR-T cells with the CD38(-)CD73(-)Tim-3(-)HLA-DR(+) phenotype predict the efficacy of tisagenlecleucel as a treatment for B cell precursor ALL.
本研究入组 19 例 BCP-ALL 患者(16 例儿童和 3 例年轻成人),接受 tisagenlecleucel 治疗。
Multiple Myeloma and Mimicry: Gastrointestinal Tract Histologic Findings in Patients Following Chimeric Antigen Receptor T-cell Therapy and Anti-CD38
我们的研究结果提示,CAR-T 治疗可引起胃肠道损伤,其特征为上皮细胞凋亡和上皮内淋巴细胞增多,并且主要累及深部黏膜的隐窝和腺体。
Intratumoral CD38(+)CD19(+)B cells associate with poor clinical outcomes and immunosuppression in patients with pancreatic ductal adenocarcinoma.
我们发现调节性 B 细胞样 CD38⁺ B 细胞浸润是胰腺导管腺癌(PDAC)的独立预后因素。
Non-ICANS neurotoxicities CD19-directed CAR T-cell therapy and the emergence of movement and neurocognitive treatment-emergent adverse events: a case
我们报告一例63岁男性弥漫性大B细胞淋巴瘤(DLBCL)患者,在接受靶向CD19的CAR T细胞疗法axicabtagene ciloleucel(axi-cel)治疗后第+22天,于初始发生CRS和ICANS之后,出现迟发性神经毒性。
Combining a CAR and a chimeric costimulatory receptor enhances T cell sensitivity to low antigen density and promotes persistence.
尽管使用针对血液系统恶性肿瘤的CAR-T细胞取得了高缓解率,仍有相当比例的患者最终出现肿瘤复发。
Trends in Nephrology: From nihilism to targeted treatment of antibody-mediated rejection.
抗CD38抗体目前构成了治疗AMR证据最强的药物类别。
Novel Therapeutic Approaches in Pediatric Acute Lymphoblastic Leukemia.
急性淋巴细胞白血病(ALL)是最常见的儿童恶性肿瘤,其特征为未成熟淋巴前体细胞的克隆性增殖。
Monospecific and Bispecific Chimeric Antigen Receptor (CAR) T-cell Therapy in Multiple Myeloma: A Systematic Review, Meta-analysis and Meta-regression
分析了 44 个队列(2 个一线队列和 42 个复发/难治性队列)的 52 篇报告,共纳入 1833 例患者。
Translating B-Cell and Plasma-Cell Targeting from Oncology to Autoimmunity: Modalities, Quantitative Bridging, and a Development Roadmap.
B 细胞通过自身抗体产生、抗原提呈和细胞因子失调,以及致病性 B 细胞或浆细胞区室的持续存在,驱动 B 细胞恶性肿瘤和多种自身免疫性疾病。
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