推车
兴奋剂
嵌合抗原受体
干扰素基因刺激剂
受体
T细胞
刺
免疫疗法
分泌物
下调和上调
免疫学
癌症研究
医学
药理学
生物
免疫系统
内科学
基因
先天免疫系统
生物化学
工程类
航空航天工程
机械工程
作者
Uğur Uslu,Lijun Sun,Sofia Castelli,Amanda Finck,Charles‐Antoine Assenmacher,Regina M. Young,Zhijian J. Chen,Carl H. June
标识
DOI:10.1038/s41467-024-47692-9
摘要
Abstract As a strategy to improve the therapeutic success of chimeric antigen receptor T cells (CART) directed against solid tumors, we here test the combinatorial use of CART and IMSA101, a newly developed stimulator of interferon genes (STING) agonist. In two syngeneic tumor models, improved overall survival is observed when mice are treated with intratumorally administered IMSA101 in addition to intravenous CART infusion. Transcriptomic analyses of CART isolated from tumors show elevated T cell activation, as well as upregulated cytokine pathway signatures, in particular IL-18, in the combination treatment group. Also, higher levels of IL-18 in serum and tumor are detected with IMSA101 treatment. Consistent with this, the use of IL-18 receptor negative CART impair anti-tumor responses in mice receiving combination treatment. In summary, we find that IMSA101 enhances CART function which is facilitated through STING agonist-induced IL-18 secretion.
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