Nanoparticle mediated cancer immunotherapy

被引:56
作者
Gupta, Jyoti [1 ,2 ]
Safdari, Haaris Ahsan [1 ,3 ]
Hoque, Mehboob [4 ]
机构
[1] Aligarh Muslim Univ, Interdisciplinary Biotechnol Unit, Aligarh 202002, Uttar Pradesh, India
[2] Indian Inst Sci, Dept Mol Reprod Dev & Genet, Bangalore 560012, Karnataka, India
[3] Indian Inst Sci, Mol Biophys Unit, Bangalore 560012, Karnataka, India
[4] Aliah Univ, Dept Biol Sci, Kolkata 700160, India
关键词
Nanoparticle; Cancer immunotherapy; Cancer vaccine; Tumor micro environment; CD8(+)T cells; Dendritic cell; Cytokines; Immune checkpoint; APOLIPOPROTEIN-A-I; GROWTH-FACTOR-BETA; T-CELL RESPONSES; DENDRITIC CELLS; TUMOR MICROENVIRONMENT; SUPPRESSOR-CELLS; MACROPHAGE POLARIZATION; IMMUNE-RESPONSES; COMBINED THERAPY; ANTIGEN;
D O I
10.1016/j.semcancer.2020.03.015
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The versatility and nanoscale size have helped nanoparticles (NPs) improve the efficacy of conventional cancer immunotherapy and opened up exciting approaches to combat cancer. This review first outlines the tumor immune evasion and the defensive tumor microenvironment (TME) that hinders the activity of host immune system against tumor. Then, a detailed description on how the NP based strategies have helped improve the efficacy of conventional cancer vaccines and overcome the obstacles led by TME. Sustained and controlled drug delivery, enhanced cross presentation by immune cells, co-encapsulation of adjuvants, inhibition of immune checkpoints and intrinsic adjuvant like properties have aided NPs to improve the therapeutic efficacy of cancer vaccines. Also, NPs have been efficient modulators of TME. In this context, NPs facilitate better penetration of the chemo-therapeutic drug by dissolution of the inhibitory meshwork formed by tumor associated cells, blood vessels, soluble mediators and extra cellular matrix in TME. NPs achieve this by suppression, modulation, or reprogramming of the immune cells and other mediators localised in TME. This review further summarizes the applications of NPs used to enhance the efficacy of cancer vaccines and modulate the TME to improve cancer immunotherapy. Finally, the hurdles faced in commercialization and translation to clinic have been discussed and intriguingly, NPs owe great potential to emerge as clinical formulations for cancer immunotherapy in near future.
引用
收藏
页码:307 / 324
页数:18
相关论文
共 228 条
  • [1] Risk Assessment and Risk Minimization in Nanomedicine: A Need for Predictive, Alternative, and 3Rs Strategies
    Accomasso, Lisa
    Cristallini, Caterina
    Giachino, Claudia
    [J]. FRONTIERS IN PHARMACOLOGY, 2018, 9
  • [2] An overview on Vadimezan (DMXAA): The vascular disrupting agent
    Adli, Amir Daei Farshchi
    Jahanban-Esfahlan, Rana
    Seidi, Khaled
    Samandari-Rad, Sonia
    Zarghami, Nosratollah
    [J]. CHEMICAL BIOLOGY & DRUG DESIGN, 2018, 91 (05) : 996 - 1006
  • [3] F-Actin Is an Evolutionarily Conserved Damage-Associated Molecular Pattern Recognized by DNGR-1, a Receptor for Dead Cells
    Ahrens, Susan
    Zelenay, Santiago
    Sancho, David
    Hanc, Pavel
    Kjaer, Svend
    Feest, Christoph
    Fletcher, Georgina
    Durkin, Charlotte
    Postigo, Antonio
    Skehel, Mark
    Batista, Facundo
    Thompson, Barry
    Way, Michael
    Sousa, Caetano Reis e
    Schulz, Oliver
    [J]. IMMUNITY, 2012, 36 (04) : 635 - 645
  • [4] Ali OA, 2009, NAT MATER, V8, P151, DOI [10.1038/nmat2357, 10.1038/NMAT2357]
  • [5] Anti-CD73 therapy impairs tumor angiogenesis
    Allard, Bertrand
    Turcotte, Martin
    Spring, Kathleen
    Pommey, Sandra
    Royal, Isabelle
    Stagg, John
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2014, 134 (06) : 1466 - 1473
  • [6] Mechanisms of action of adjuvants
    Awate, Sunita
    Babiuk, Lorne A.
    Mutwiri, George
    [J]. FRONTIERS IN IMMUNOLOGY, 2013, 4
  • [7] Imatinib potentiates antitumor T cell responses in gastrointestinal stromal tumor through the inhibition of Ido
    Balachandran, Vinod P.
    Cavnar, Michael J.
    Zeng, Shan
    Bamboat, Zubin M.
    Ocuin, Lee M.
    Obaid, Hebroon
    Sorenson, Eric C.
    Popow, Rachel
    Ariyan, Charlotte
    Rossi, Ferdinand
    Besmer, Peter
    Guo, Tianhua
    Antonescu, Cristina R.
    Taguchi, Takahiro
    Yuan, Jianda
    Wolchok, Jedd D.
    Allison, James P.
    DeMatteo, Ronald P.
    [J]. NATURE MEDICINE, 2011, 17 (09) : 1094 - U99
  • [8] Oxidized Multiwalled Carbon Nanotubes as Antigen Delivery System to Promote Superior CD8+ T Cell Response and Protection against Cancer
    Batista de Faria, Paula Cristina
    dos Santos, Luara Isabela
    Coelho, Joao Paulo
    Ribeiro, Henrique Buecker
    Pimenta, Marcos Assuncao
    Ladeira, Luiz Orlando
    Gomes, Dawidson Assis
    Furtado, Clascidia Aparecida
    Gazzinelli, Ricardo Tostes
    [J]. NANO LETTERS, 2014, 14 (09) : 5458 - 5470
  • [9] Elimination of Metastatic Melanoma Using Gold Nanoshell-Enabled Photothermal Therapy and Adoptive T Cell Transfer
    Bear, Adham S.
    Kennedy, Laura C.
    Young, Joseph K.
    Perna, Serena K.
    Almeida, Joao Paulo Mattos
    Lin, Adam Y.
    Eckels, Phillip C.
    Drezek, Rebekah A.
    Foster, Aaron E.
    [J]. PLOS ONE, 2013, 8 (07):
  • [10] Targeting proteins to distinct subcellular compartments reveals unique requirements for MHC class I and II presentation
    Belizaire, Roger
    Unanue, Emil R.
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (41) : 17463 - 17468