耐火材料(行星科学)
体内
淋巴瘤
病毒
癌症研究
病毒学
医学
生物
免疫学
生物技术
天体生物学
作者
Xinfeng Chen,Ke Huang,Jin-Yan Liu,Yuhang Li,Guohui Qin,Mingzhi Zhang,Ying Zhang
标识
DOI:10.1136/jitc-2024-sitc2024.1482
摘要
Background
More than ten autologous CAR-T cell products have been approved for the treatment of relapsed or refractory hematological malignancies, but still some patients cannot benefit due to the complex manufacture, high cost or rapid disease progression. Methods
To tackle this dilemma, researchers developed in-vivo CAR-T cell therapy using specific virus or mRNA to explore the universally ‘off-the-shelf’ product. Results
Here, we reported the first-in-human, investigator-initiated clinical trial, to evaluate the safety and efficacy of in-vivo CAR-T cells targeted CD19 generated from specific virus in patients with B-cell non-Hodgkin’s lymphoma (figure 1). A 64-year-old male patient with relapsed/refractory diffuse large B-cell lymphoma achieved a partial remission on day 35 after infusion with specific virus induced in-vivo CAR-T cells. The expansion peak of CAR-T cells in vivo was observed on day 17 days after treatment. The major side effects were myelotoxicity and grade 1 of cytokine release syndrome. No neurotoxicity or infection was observed. Conclusions
To our knowledge, this was the first report demonstrated in-vivo CAR-T cells produced significant anti-tumor ability in patients with B-NHL. These data validate and support the efficacy and safety of in-vivo CAR-T cells in preclinical and clinical trials, providing a paradigm shift in the field of CAR-T cell therapies.
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