Targeting drugs to tumours using cell membrane-coated nanoparticles

被引:547
作者
Fang, Ronnie H. [1 ,2 ]
Gao, Weiwei [1 ,2 ]
Zhang, Liangfang [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept NanoEngn, Chem Engn Program, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
ANTIGEN-PRESENTING CELLS; RED-BLOOD-CELLS; ERYTHROCYTE-MEMBRANE; POLYMERIC NANOPARTICLES; CANCER-IMMUNOTHERAPY; BIOMIMETIC NANOPARTICLES; MACROPHAGE-MEMBRANE; RBC MEMBRANES; DELIVERY; FUNCTIONALIZATION;
D O I
10.1038/s41571-022-00699-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Owing to several limitations, including elimination by the immune system and a lack of tumour specificity, systemically administered synthetic nanoparticles are used for a limited range of cancer indications. In this Review, the authors describe the potential of cellular nanoparticles (comprising a cell membrane coating around a synthetic core) to overcome these issues as well as their application in drug delivery, phototherapy and immunotherapy. Traditional cancer therapeutics, such as chemotherapies, are often limited by their non-specific nature, causing harm to non-malignant tissues. Over the past several decades, nanomedicine researchers have sought to address this challenge by developing nanoscale platforms capable of more precisely delivering drug payloads. Cell membrane-coated nanoparticles (CNPs) are an emerging class of nanocarriers that have demonstrated considerable promise for biomedical applications. Consisting of a synthetic nanoparticulate core camouflaged by a layer of naturally derived cell membranes, CNPs are adept at operating within complex biological environments; depending on the type of cell membrane utilized, the resulting biomimetic nanoformulation is conferred with several properties typically associated with the source cell, including improved biocompatibility, immune evasion and tumour targeting. In comparison with traditional functionalization approaches, cell membrane coating provides a streamlined method for creating multifunctional and multi-antigenic nanoparticles. In this Review, we discuss the history and development of CNPs as well as how these platforms have been used for cancer therapy. The application of CNPs for drug delivery, phototherapy and immunotherapy will be described in detail. Translational efforts are currently under way and further research to address key areas of need will ultimately be required to facilitate the successful clinical adoption of CNPs.
引用
收藏
页码:33 / 48
页数:16
相关论文
共 161 条
[1]   The accelerated blood clearance (ABC) phenomenon: Clinical challenge and approaches to manage [J].
Abu Lila, Amr S. ;
Kiwada, Hiroshi ;
Ishida, Tatsuhiro .
JOURNAL OF CONTROLLED RELEASE, 2013, 172 (01) :38-47
[2]   Surface Glycan Modification of Cellular Nanosponges to Promote SARS-CoV-2 Inhibition [J].
Ai, Xiangzhao ;
Wang, Dan ;
Honko, Anna ;
Duan, Yaou ;
Gavrish, Igor ;
Fang, Ronnie H. ;
Griffiths, Anthony ;
Gao, Weiwei ;
Zhang, Liangfang .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2021, 143 (42) :17615-17621
[3]   Nanoparticles in the clinic [J].
Anselmo, Aaron C. ;
Mitragotri, Samir .
BIOENGINEERING & TRANSLATIONAL MEDICINE, 2016, 1 (01) :10-29
[4]  
Aryal S, 2013, NANOMEDICINE-UK, V8, P1271, DOI [10.2217/NNM.12.153, 10.2217/nnm.12.153]
[5]   In vitro clinical-grade generation of red blood cells from human umbilical cord blood CD34+cells [J].
Baek, Eun Jung ;
Kim, Han-Soo ;
Kim, Sinyoung ;
Jin, Honglien ;
Choi, Tae-Yeal ;
Kim, Hyun Ok .
TRANSFUSION, 2008, 48 (10) :2235-2245
[6]   Intratumoral immunotherapy using platelet-cloaked nanoparticles enhances antitumor immunity in solid tumors [J].
Bahmani, Baharak ;
Gong, Hua ;
Luk, Brian T. ;
Haushalter, Kristofer J. ;
DeTeresa, Ethel ;
Previti, Mark ;
Zhou, Jiarong ;
Gao, Weiwei ;
Bui, Jack D. ;
Zhang, Liangfang ;
Fang, Ronnie H. ;
Zhang, Jie .
NATURE COMMUNICATIONS, 2021, 12 (01)
[7]   Doxil® - The first FDA-approved nano-drug: Lessons learned [J].
Barenholz, Yechezkel .
JOURNAL OF CONTROLLED RELEASE, 2012, 160 (02) :117-134
[8]   Tumor Cell-Derived Extracellular Vesicle-Coated Nanocarriers: An Efficient Theranostic Platform for the Cancer-Specific Delivery of Anti-miR-21 and Imaging Agents [J].
Bose, Rajendran J. C. ;
Kumar, Sukumar Uday ;
Zeng, Yitian ;
Afjei, Rayhaneh ;
Robinson, Elise ;
Lau, Kenneth ;
Bermudez, Abel ;
Habte, Frezghi ;
Pitteri, Sharon J. ;
Sinclair, Robert ;
Willmann, Juergen K. ;
Massoud, Tarik F. ;
Gambhir, Sanjiv S. ;
Paulmurugan, Ramasamy .
ACS NANO, 2018, 12 (11) :10817-10832
[9]   Cancer-related fatigue-mechanisms, risk factors, and treatments [J].
Bower, Julienne E. .
NATURE REVIEWS CLINICAL ONCOLOGY, 2014, 11 (10) :597-609
[10]   Tangential Flow Filtration for Highly Efficient Concentration of Extracellular Vesicles from Large Volumes of Fluid [J].
Busatto, Sara ;
Vilanilam, George ;
Ticer, Taylor ;
Lin, Wen-Lang ;
Dickson, Dennis W. ;
Shapiro, Shane ;
Bergese, Paolo ;
Wolfram, Joy .
CELLS, 2018, 7 (12)