光热治疗
重编程
钙网蛋白
材料科学
免疫原性细胞死亡
肿瘤微环境
靶向治疗
吲哚青绿
纳米技术
癌症研究
免疫疗法
癌症
肿瘤细胞
病理
化学
医学
细胞生物学
生物
内科学
细胞
内质网
生物化学
作者
Liuhai Zheng,Huifang Wang,Xiaoru Zhong,Jia Horng Lin,Guangwei Shi,Chongzhi Bai,Runwei Yang,Zhenhui Huang,Yuke Jiang,Jinxi Wei,Zhiyu Dong,Jiexuan Li,Ying Long,Lingyun Dai,Zhijie Li,Chunbo Chen,Jigang Wang
出处
期刊:Biomaterials
[Elsevier]
日期:2024-09-04
卷期号:314: 122809-122809
标识
DOI:10.1016/j.biomaterials.2024.122809
摘要
Targeted therapies have revolutionized traditional cancer treatments by precisely targeting tumor cells, enhancing efficacy and safety. Despite this advancement, the proportion of cancer patients eligible for such therapies remains low due to the absence of suitable targets. Here, we investigate whether the translocation of the immunogenic cell death (ICD) marker calreticulin (CALR) from the endoplasmic reticulum (ER) to the cell surface following ICD induction can serve as a target for targeted therapies. To target CALR, a nanobody Nb215 identified from a naïve VHH phage library with high binding affinity to both human and mouse CALR was employed to engineer probiotic EcN 1917. Our results demonstrated that CALR nanobody-modified EcN-215 coupled with the photothermal dye indocyanine green (ICG) was able to exert NIR-II imaging-guide photothermal therapy (PTT). Moreover, PTT with EcN-215/ICG can reshape the tumor microenvironment by enhancing the infiltration of CD45
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