| Literature DB >> 32661094 |
Pingwei Xu1, Ke Tang1, Jingwei Ma1, Huafeng Zhang1, Dianheng Wang1, Liyan Zhu1, Jie Chen1, Keke Wei1, Jincheng Liu1, Haiqing Fang1, Liang Tang1, Yi Zhang2, Jing Xie2, Yuying Liu2, Rui Meng3, Li Liu3, Xiaorong Dong3, Kunyu Yang3, Gang Wu3, Fei Ma4, Bo Huang5,2,6.
Abstract
Malignant pleural effusion (MPE) is a frequent complication of various cancers and often leads to a poor quality of life, prognosis, and life expectancy, and its management remains palliative. New approaches that can effectively treat MPE are highly desirable. Here, we show that methotrexate (MTX)-packaging tumor cell-derived microparticles (MTX-MP) act as an effective immunotherapeutic agent to treat patients with MPE by mobilizing and activating neutrophils. We find that MTX-MP perfusion via a pleural catheter elicits the recruitment of neutrophils in patients through macrophage-released CXCL1 and CXCL2. By performing ex vivo experiments, we find that the recruited neutrophils are activated and release reactive oxygen species (ROS) and neutrophil extracellular trap (NET) to kill tumor cells. Neutrophil-released NETs were also able to seal off the damaged endothelium, facilitating MPE resolution in vitro and in tumor-bearing mice. These findings reveal the potential for use of cell-derived materials to package drugs as an immunotherapeutic agent against MPE. ©2020 American Association for Cancer Research.Entities:
Year: 2020 PMID: 32661094 DOI: 10.1158/2326-6066.CIR-19-0789
Source DB: PubMed Journal: Cancer Immunol Res ISSN: 2326-6066 Impact factor: 11.151