Immunoadjuvants for cancer immunotherapy: A review of recent developments. (15th September 2020)
- Record Type:
- Journal Article
- Title:
- Immunoadjuvants for cancer immunotherapy: A review of recent developments. (15th September 2020)
- Main Title:
- Immunoadjuvants for cancer immunotherapy: A review of recent developments
- Authors:
- Banstola, Asmita
Jeong, Jee-Heon
Yook, Simmyung - Abstract:
- Abstract: Cancer immunotherapy evolved as a new treatment modality to eradicate tumor cells and has gained in popularity after its successful clinical transition. By activating antigen-presenting cells (APCs), and thus, inducing innate or adaptive immune responses, immunoadjuvants have become promising tools for cancer immunotherapy. Different types of immunoadjuvants such as toll-like receptor (TLR) agonists, exosomes, and metallic and plant-derived immunoadjuvants have been studied for their immunological effects. However, the clinical use of immunoadjuvants is limited by short response rates and various side-effects. The rapid progress made in the development of nanoparticle systems as immunoadjuvant carrier vehicles has provided potential carriers for cancer immunotherapy. In this review article, we describe different types of immunoadjuvants, their limitations, modes of action, and the reasons for their clinical adoption. In addition, we review recent progress made in the nanoparticle-based immunoadjuvant field and on the combined use of nanoparticle-based immunoadjuvants and chemotherapy, phototherapy, radiation therapy, and immune checkpoint inhibitor-based therapy. Statement of Significance: Cancer immunotherapy emerged as a new hope for treating malignant tumors. Different types of immunoadjuvants serve as an important tool for cancer immunotherapy by activating an innate or adaptive immune response. Limitation of free immunoadjuvant has paved the path for theAbstract: Cancer immunotherapy evolved as a new treatment modality to eradicate tumor cells and has gained in popularity after its successful clinical transition. By activating antigen-presenting cells (APCs), and thus, inducing innate or adaptive immune responses, immunoadjuvants have become promising tools for cancer immunotherapy. Different types of immunoadjuvants such as toll-like receptor (TLR) agonists, exosomes, and metallic and plant-derived immunoadjuvants have been studied for their immunological effects. However, the clinical use of immunoadjuvants is limited by short response rates and various side-effects. The rapid progress made in the development of nanoparticle systems as immunoadjuvant carrier vehicles has provided potential carriers for cancer immunotherapy. In this review article, we describe different types of immunoadjuvants, their limitations, modes of action, and the reasons for their clinical adoption. In addition, we review recent progress made in the nanoparticle-based immunoadjuvant field and on the combined use of nanoparticle-based immunoadjuvants and chemotherapy, phototherapy, radiation therapy, and immune checkpoint inhibitor-based therapy. Statement of Significance: Cancer immunotherapy emerged as a new hope for treating malignant tumors. Different types of immunoadjuvants serve as an important tool for cancer immunotherapy by activating an innate or adaptive immune response. Limitation of free immunoadjuvant has paved the path for the development of nanoparticle-based immunoadjuvant therapy with the hope of prolonging the therapeutic efficacy. This review highlights the recent advancement made in nanoparticle-based immunoadjuvant therapy in modulating the adaptive and innate immune system. The application of the combinatorial approach of chemotherapy, phototherapy, radiation therapy adds synergy in nanoparticle-based immunoadjuvant therapy. It will broaden the reader's understanding on the recent progress made in immunotherapy with the aid of immunoadjuvant-based nanosystem. Graphical abstract: Image, graphical abstract … (more)
- Is Part Of:
- Acta biomaterialia. Volume 114(2020)
- Journal:
- Acta biomaterialia
- Issue:
- Volume 114(2020)
- Issue Display:
- Volume 114, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 114
- Issue:
- 2020
- Issue Sort Value:
- 2020-0114-2020-0000
- Page Start:
- 16
- Page End:
- 30
- Publication Date:
- 2020-09-15
- Subjects:
- Immunoadjuvant -- Exosome -- Toll-like receptor -- Phototherapy -- Immune checkpoint inhibitor
APCs Antigen-presenting cells -- TLR Toll-like receptor -- Treg Regulatory T cells -- DCs Dendritic cells -- MHC I Major histocompatibility complex I -- DAMPs Damage-associated molecular patterns -- NK cells Natural killer cells -- poly I:C Polyinosinic-polycytidylic acid -- IL Interleukin -- IFN-γ Interferon-gamma -- MPL 3-o-desacyl-4′- monophosphoryl lipid a -- BCG Bacillus calmette-guerin -- IFNα Interferon-alpha -- pDCs Plasmacytoid dendritic cells -- R837 Imiquimoid -- R848 Resiquimod -- CpG Cytosine and guanine incorporating motifs -- ODNs Oligodeoxynucleotides -- IDO Indoleamine 2, 3-dioxygenase -- Al2O3 Aluminum oxide nanoparticles -- Mg Magnesium -- GO Graphene oxide -- ISCOMs Immune-stimulatory complexes -- QS-21 Quillaja Saponaria tree -- HSPs Heat-shock proteins -- HMGB1 high mobility group box 1 molecules -- PLGA-NPs poly lactic-co-glycolic acid nanoparticles -- TRP2 tyrosine related protein II -- GM-CSF granulocyte-macrophage colony-stimulating factor -- ICG indocyanine green -- HCuSNPs hollow copper sulfide nanoparticles -- PEG polyethylene glycol -- PEI polyethylenimine -- BSA bovine serum albumin -- GNRs gold nanorods -- HA hyaluronic acid -- sHDLs synthetic high-density lipoprotein nanoparticles -- ICIs immune checkpoint inhibitors -- NSCLC non-small-cell lung cancer
Biomedical materials -- Periodicals
610.28 - Journal URLs:
- http://www.sciencedirect.com/science/journal/17427061 ↗
http://www.elsevier.com/wps/find/journaldescription.cws%5Fhome/702994/description ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.actbio.2020.07.063 ↗
- Languages:
- English
- ISSNs:
- 1742-7061
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0602.900500
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