Elsevier

Molecular Immunology

Volume 87, July 2017, Pages 227-239
Molecular Immunology

Review article
Epigenetics and immunotherapy: The current state of play

https://doi.org/10.1016/j.molimm.2017.04.012Get rights and content
Under a Creative Commons license
open access

Highlights

  • Epigenetic immunomodulation plays a key role tumour immune escape.

  • Epigenetic therapy can prime and sensitise the host immune response to subsequent immunotherapeutic strategies.

  • Combined epigenetic and immunotherapy holds significant promise for improved patient outcomes in many different cancer types.

Abstract

Cancer cells employ a number of mechanisms to escape immunosurveillance and facilitate tumour progression. The recent explosion of interest in immunotherapy, especially immune checkpoint blockade, is a result of discoveries about the fundamental ligand-receptor interactions that occur between immune and cancer cells within the tumour microenvironment. Distinct ligands expressed by cancer cells engage with cell surface receptors on immune cells, triggering inhibitory pathways (such as PD-1/PD-L1) that render immune cells immunologically tolerant. Importantly, recent studies on the role of epigenetics in immune evasion have exposed a key role for epigenetic modulators in augmenting the tumour microenvironment and restoring immune recognition and immunogenicity. Epigenetic drugs such as DNA methyltransferase and histone deacetylase inhibitors can reverse immune suppression via several mechanisms such as enhancing expression of tumour-associated antigens, components of the antigen processing and presenting machinery pathways, immune checkpoint inhibitors, chemokines, and other immune-related genes. These discoveries have established a highly promising basis for studies using combined epigenetic and immunotherapeutic agents as anti-cancer therapies. In this review, we discuss the exciting role of epigenetic immunomodulation in tumour immune escape, emphasising its significance in priming and sensitising the host immune system to immunotherapies through mechanisms such as the activation of the viral defence pathway. With this background in mind, we highlight the promise of combined epigenetic therapy and immunotherapy, focusing on immune checkpoint blockade, to improve outcomes for patients with many different cancer types.

Abbreviations

TME
tumour microenvironment
PD-1
programmed cell death 1
PD-L1
programmed death ligand 1
PD-L2
programmed death ligand 2
PTMs
post-translational histone modifications
DNMTi
DNA methyltransferase inhibitor
HDACi
histone deacetylase inhibitor
TAA
tumour-associated antigens
APM
antigen processing and presentation machinery
NK
natural killer
NKG2D
NK group 2D
MICA/B
MHC class I-related chain A/B
ULBPs
ULB16-binding proteins
TRAIL
TNF-related-apoptosis inducing ligand
FASL
FAS ligand
DC
dendritic cell
APC
antigen presenting cells
TFH
T follicular helper
Treg
regulatory T cell
CTL
cytotoxic T lymphocyte
TCR
T cell receptor
HLA
human leukocyte antigen
TAP
transporter associated with antigen presenting
ICAM-1
intercellular adhesion molecule 1
TILs
tumour-infiltrating lymphocytes
CTLA-4
cytotoxic T lymphocyte antigen 4
TNBC
:triple-negative breast cancer
NSCLC
non-small cell lung cancer
AML
acute myeloid leukaemia
CCL
chronic lymphatic leukaemia
mAb
monoclonal antibody
FDA
Food and Drug administration
Ig
immunoglobin
PI3K
phosphoinositide 3-kinase
MDSC
myeloid-derived suppressor cell
CAF
cancer-associated fibroblast
CSC
cancer stem cell
HGF
hepatocyte grown factor
CTAs
cancer testis antigens
HMW-MAA
high molecular weight melanoma-associated protein
Th1
T helper 1
EZH2
enhancer of zeste homologue 2
H3K27
me3: histone 3 lysing 27 trimethylation
DNMT1
DNA methyltransferase 1
ERVs
endogenous retroviral sequences
5-AZA-dC
5-aza-2′-deoxycytidine

Keywords

Epigenetics
Immunotherapy
Immune checkpoint blockade
Combination therapy
DNA methyltransferase inhibitors
Histone deacetylase inhibitors

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