| Literature DB >> 30063143 |
Xudong Zhang1,2,3, Jinqiang Wang2,3, Zhaowei Chen3, Quanyin Hu3, Chao Wang3, Junjie Yan3, Gianpietro Dotti4, Peng Huang1, Zhen Gu2,3.
Abstract
Radical surgery still represents the treatment choice for several malignancies. However, local and distant tumor relapses remain the major causes of treatment failure, indicating that a postsurgery consolidation treatment is necessary. Immunotherapy with checkpoint inhibitors has elicited impressive clinical responses in several types of human malignancies and may represent the ideal consolidation treatment after surgery. Here, we genetically engineered platelets from megakaryocyte (MK) progenitor cells to express the programmed cell death protein 1 (PD-1). The PD-1 platelet and its derived microparticle could accumulate within the tumor surgical wound and revert exhausted CD8+ T cells, leading to the eradication of residual tumor cells. Furthermore, when a low dose of cyclophosphamide (CP) was loaded into PD-1-expressing platelets to deplete regulatory T cells (Tregs), an increased frequency of reinvigorated CD8+ lymphocyte cells was observed within the postsurgery tumor microenvironment, directly preventing tumor relapse.Entities:
Keywords: Drug delivery; immune checkpoint blockade; immunotherapy; nanomedicine; platelet
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Year: 2018 PMID: 30063143 DOI: 10.1021/acs.nanolett.8b02321
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189