免疫疗法
癌症免疫疗法
肽聚糖
癌症研究
免疫佐剂
体内
肿瘤微环境
医学
放射治疗
癌症
免疫系统
免疫学
化学
内科学
生物
肿瘤细胞
生物化学
酶
生物技术
作者
Xinhong Li,Yi‐Ting Chen,Rui Wang,Enhao Lu,Kuankuan Luo,Xianyi Sha
标识
DOI:10.1016/j.ijpharm.2023.123430
摘要
Immunotherapy has achieved some success in preclinical and clinical studies, but the immunosuppressive tumor microenvironment (TME) leads to a low response rate of this therapy. In this paper, we describe a calreticulin (CRT) valgus CT-26 tumor cell membranes-coated bacterial whole peptidoglycan (WPG) from P. aeruginosa (CPW/SR) with a high rate of the STING agonist loading. In the construct, WPG from P. aeruginosa (P.WPG) was used as a carrier with the immunoadjuvant function while synergistically promoting the maturation of dendritic cells (DCs) through the delivery of the STING agonist SR-717. CRT valgus tumor cell membranes were identified and internalized by DCs via CRT on the surface. In addition, this construct was able to reverse the immunosuppressive TME in vivo and achieve synergies with radiotherapy by creating a personalized tumor vaccine, therefore achieving more resultful antitumor efficacy. In conclusion, CPW/SR constructed in this paper provides a new approach for achieving efficient cancer immunotherapy and combination therapy.
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