Review
Application of dendritic cells in tumor immunotherapy and progress in the mechanism of anti-tumor effect of Astragalus polysaccharide (APS) modulating dendritic cells: a review

https://doi.org/10.1016/j.biopha.2022.113541Get rights and content
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Highlights

  • Dendritic cells (DCs), as antigen-presenting cells, play an important role in the body's immune and tumor-fighting processes.

  • During tumor development, dendritic cells (DCs) induce not only antitumor immune responses but also tumor immune tolerance.

  • The antitumor effect of astragalus polysaccharide (APS) is closely related to DCs, which promotes the maturation of DCs and activates CTL to exert antitumor effects.

  • Astragalus polysaccharide (APS) in combination with DCs tumor vaccine enhances the antigen presentation of DCs.

Abstract

Dendritic cells (DCs) are potent antigen-presenting cells (APCs) that are essential in mediating the body's natural and adaptive immune responses. The body can regulate the function of DCs in various ways to enhance their antitumor effects. In the tumour microenvironment (TME), antigen-specific T cell responses are initiated through DC processing and delivery of tumour-associated antigens (TAAs); conversely, tumour cells inhibit DC recruitment by releasing metabolites, cytokines and other regulatory TME and function. Different subpopulations of DCs exist in tumour tissues, and their functions vary. Insight into DC subgroups in TME allows assessment of the effectiveness of tumour immunotherapy. Astragalus polysaccharide (APS) is the main component of the Chinese herb Astragalus membranaceus. The study found that the antitumor effects of APS are closely related to DCs. APS can promote the expression of surface molecules CD80 and CD86, promote the maturation of DCs, and activate CTL to exert antitumor effects. We reviewed the application of DCs in tumor immunotherapy and the mechanism of modulation of DCs by Astragalus polysaccharide to provide new directions and strategies for tumor therapy and new drug development.

Abbreviations

FDA
Food and Drug Administration
AAV
adeno-associated virus
DCs
Dendritic cells
TME
tumor microenvironment
TAAs
tumor-associated antigens
APS
Astragalus polysaccharide
CTL
Cytotoxic T lymphocyte
TLR4
Toll-like receptor 4
APCs
antigen presenting cells
LCs
Langerhans cells
RA
retinoic acid
TGF-β
transforming growth factor-β
moDCs
monocyte-derived DCs
pDCs
plasma cell DCs
TCR
MHC-T cell receptor
FLT3L
Fms-like tyrosine kinase
GM-CSF
Granulocyte-macrophage Colony Stimulating Factor
Th1
type 1 helper T cell
NF-κB
nuclear factor-κB
HMGB;1
high mobility group protein
PFS
progression-free survival
NK
natural killer cell
PD-L1
Programmed cell death 1 ligand1
IDO1
indoleamine2,3-dioxygenase1
CTLA4
cytotoxicT-lymphocyte-associated protein 4
FOXO1
Forked head transcription factor 1
PI3K
Phosphatidylinositol-3 kinase
MyD88
myeloid differentiation factor 88
LKB1
Liver kinase B1
IL
Interleukin

Keywords

Dendritic cells
DC vaccine
DC subgroups
Astragalus polysaccharide
Tumor microenvironm

Data Availability

No data was used for the research described in the article.

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