Nanomedicines modulating tumor immunosuppressive cells to enhance cancer immunotherapy

被引:82
作者
Zhu, Yuefei [1 ,2 ]
Yu, Xiangrong [3 ]
Thamphiwatana, Soracha D. [4 ]
Zheng, Ying [5 ]
Pang, Zhiqing [2 ]
机构
[1] Columbia Univ, Dept Biomed Engn, New York, NY 10027 USA
[2] Fudan Univ, Sch Pharm, Key Lab Smart Drug Delivery, Minist Educ, Shanghai 201203, Peoples R China
[3] Jinan Univ, Zhuhai Peoples Hosp, Zhuhai Hosp, Dept Med Imaging, Zhuhai 519000, Peoples R China
[4] Mahidol Univ, Fac Engn, Dept Biomed Engn, Salaya 73170, Nakhon Pathom, Thailand
[5] Univ Macau, Inst Chinese Med Sci, State Key Lab Qual Res Chinese Med, Macau 999078, Peoples R China
基金
中国国家自然科学基金;
关键词
Cancer immunotherapy; Nanomedicine; Tumor immunosuppressive microenvironment; Drug delivery; REGULATORY T-CELLS; SUPPRESSOR-CELLS; B-CELLS; DENDRITIC CELLS; INFLAMMATORY MONOCYTES; HYBRID NANOPARTICLES; TARGETED DELIVERY; VACCINE THERAPY; IN-VIVO; MICROENVIRONMENT;
D O I
10.1016/j.apsb.2020.08.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cancer immunotherapy has veered the paradigm of cancer treatment. Despite recent advances in immunotherapy for improved antitumor efficacy, the complicated tumor microenvironment (TME) is highly immunosuppressive, yielding both astounding and unsatisfactory clinical successes. In this regard, clinical outcomes of currently available immunotherapy are confined to the varied immune systems owing in large part to the lack of understanding of the complexity and diversity of the immune context of the TME. Various advanced designs of nanomedicines could still not fully surmount the delivery barriers of the TME. The immunosuppressive TME may even dampen the efficacy of antitumor immunity. Recently, some nanotechnology-related strategies have been inaugurated to modulate the immunosuppressive cells within the tumor immune microenvironment (TIME) for robust immunotherapeutic responses. In this review, we will highlight the current understanding of the immunosuppressive TIME and identify disparate subclasses of TIME that possess an impact on immunotherapy, especially those unique classes associated with the immunosuppressive effect. The immunoregulatory cell types inside the immunosuppressive TIME will be delineated along with the existing and potential approaches for immunosuppressive cell modulation. After introducing the various strategies, we will ultimately outline both the novel therapeutic targets and the potential issues that affect the efficacy of TIME-based nanomedicines. (C) 2020 Chinese Pharmaceutical Association and Institute of Materia Medica, Chinese Academy of Medical Sciences. Production and hosting by Elsevier B.V.
引用
收藏
页码:2054 / 2074
页数:21
相关论文
共 194 条
[1]   Immunosuppressive activities of adenosine in cancer [J].
Allard, Bertrand ;
Beavis, Paul A. ;
Darcy, Phillip K. ;
Stagg, John .
CURRENT OPINION IN PHARMACOLOGY, 2016, 29 :7-16
[2]   Comparison of acute toxicity and mortality after two different dosing regimens of high-dose interleukin-2 for patients with metastatic melanoma [J].
Alwan, Laura M. ;
Grossmann, Kenneth ;
Sageser, Daniel ;
Van Atta, Joan ;
Agarwal, Neeraj ;
Gilreath, Jeffrey A. .
TARGETED ONCOLOGY, 2014, 9 (01) :63-71
[3]   Impact of molecular weight on the intrinsic immunogenic activity of poly(beta amino esters) [J].
Andorko, James I. ;
Pineault, Kevin G. ;
Jewell, Christopher M. .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2017, 105 (04) :1219-1229
[4]   Intrinsic immunogenicity of rapidly-degradable polymers evolves during degradation [J].
Andorko, James I. ;
Hess, Krystina L. ;
Pineault, Kevin G. ;
Jewell, Christopher M. .
ACTA BIOMATERIALIA, 2016, 32 :24-34
[5]   Targeting Macrophage-Recruiting Chemokines as a Novel Therapeutic Strategy to Prevent the Progression of Solid Tumors [J].
Argyle, David ;
Kitamura, Takanori .
FRONTIERS IN IMMUNOLOGY, 2018, 9
[6]   Dynamic Treg interactions with intratumoral APCs promote local CTL dysfunction [J].
Bauer, Christian A. ;
Kim, Edward Y. ;
Marangoni, Francesco ;
Carrizosa, Esteban ;
Claudio, Natalie M. ;
Mempel, Thorsten R. .
JOURNAL OF CLINICAL INVESTIGATION, 2014, 124 (06) :2425-2440
[7]   Exclusion of T Cells From Pancreatic Carcinomas in Mice Is Regulated by Ly6Clow F4/80+ Extratumoral Macrophages [J].
Beatty, Gregory L. ;
Winograd, Rafael ;
Evans, Rebecca A. ;
Long, Kristen B. ;
Luque, Santiago L. ;
Lee, Jae W. ;
Clendenin, Cynthia ;
Gladney, Whitney L. ;
Knoblock, Dawson M. ;
Guirnalda, Patrick D. ;
Vonderheide, Robert H. .
GASTROENTEROLOGY, 2015, 149 (01) :201-210
[8]  
Benito Jardon M, 2017, ELIFE, V6
[9]   Understanding the tumor immune microenvironment (TIME) for effective therapy [J].
Binnewies, Mikhail ;
Roberts, Edward W. ;
Kersten, Kelly ;
Chan, Vincent ;
Fearon, Douglas F. ;
Merad, Miriam ;
Coussens, Lisa M. ;
Gabrilovich, Dmitry I. ;
Ostrand-Rosenberg, Suzanne ;
Hedrick, Catherine C. ;
Vonderheide, Robert H. ;
Pittet, Mikael J. ;
Jain, Rakesh K. ;
Zou, Weiping ;
Howcroft, T. Kevin ;
Woodhouse, Elisa C. ;
Weinberg, Robert A. ;
Krummel, Matthew F. .
NATURE MEDICINE, 2018, 24 (05) :541-550
[10]   Immunosuppressive and Prometastatic Functions of Myeloid-Derived Suppressive Cells Rely upon Education from Tumor-Associated B Cells [J].
Bodogai, Monica ;
Moritoh, Kanako ;
Lee-Chang, Catalina ;
Hollander, Christine M. ;
Sherman-Baust, Cheryl A. ;
Wersto, Robert P. ;
Araki, Yoshihiko ;
Miyoshi, Ichiro ;
Yang, Li ;
Trinchieri, Giorgio ;
Biragyn, Arya .
CANCER RESEARCH, 2015, 75 (17) :3456-3465