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Table 6 Immune checkpoint inhibitors (ICIs) combination therapy with oncolytic viruses (OVs) (animal study)

From: Tumor immunotherapies by immune checkpoint inhibitors (ICIs); the pros and cons

Tumor

Target ICs

OVs type

Main result

References

Glioma

CTLA-4

PD-1

IL-12-expressing oHSV

Induction of macrophage influx and M1-like polarization and improving T effector (CD4+ and CD8+ T cells) to T regulatory cell ratio

[297, 298]

Rectal cancer

PD-1

hTERT-expressing oAd

Tumor regression by recruitment of CTLs

[299]

Osteosarcoma

PD-1

hTERT-expressing oAd

Tumor regression by recruitment of CTLs

[299]

Breast cancer

PD-1

CTLA-4

Soluble TGFβRIIFc-expressing oAd

Inhibition of tumor growth and lung and liver metastases

[300]

Lung cancer

Breast cancer

Melanoma

Lymphoma

PD-1

PD-L1

CTLA-4

GM-CSF-expressing oHSV-1

Tumor regression and also induction of immunological memory

[300]

Glioblastoma multiforme (GBM)

PD-1

ZIKV

Improved survival of treated animals

[301]

Rhabdomyosarcoma

PD-1

oHSV

Amelioration of incidence of CD4+ and CD8+ T cells but not Treg populations in the tumor

[302]

Melanoma

PD-L1

oHSV

Enhancing IFNγ-producing CD8+ TILs

Improved survival of treated animals

[303]

Lung adenocarcinoma

PD-1

oAd

Inhibition of tumor cell dissemination in a CD8 T-cell-dependent manner

[304]

Melanoma

PD-1

PD-L1

CTLA-4

CD40L-expressing oAd

Increasing the systemic level of tumor-specific CD8+ T cells, and also promoting the ratio of intratumoral CD8+ T cells to Treg

[245]

GBM

PD-L1

CD40L-expressing oAd

Inhibition of tumor development associated with increased survival

[305]

Prostate cancer

PD-1

oAd

Induction of antigen-specific CD8+ T-cell responses in mice

[306]

Melanoma

PD-1

oAd

Delayed tumor growth leading to the boosted survival of treated animal

[307]

Melanoma

PD-1

Reovirus

Enhanced capacity of NK cells to eliminate reovirus-infected tumor cells, abridged Treg activity and augmented the CD8+ T-cell-mediated antitumor response

[308]

GBM

PD-1

Reovirus

Improving the expression of IFN-regulated gene expression, as well as the PD-1/PD-L1 axis in tumors

[309]

GBM

PD-1

CTLA-4

HIF-2α, Sox-10, c-Myc, and TRP1-expressing VSV

Restoring the antitumor Th1 interferon-γ and Th17 T cell responses

[310]

Melanoma

PD-L1

MV

Inducing tumor remission

[311]

GBM

PD-1

EGFR-expressing MV

Improved inflammatory cell influx into the brains of treated mice

Enhanced overall survival in treated animal

[312]

  1. Programmed cell death protein 1 (PD-1), programmed death-ligand 1 (PD-L1), cytotoxic-T-lymphocyte-associated protein 4 (CTLA-4), interferon-gamma (IFNγ), regulatory T cells (Tregs), tumor-infiltrating lymphocytes (TILs), natural killer (NK) cell, cytotoxic T lymphocytes (CTLs), oncolytic herpes simplex virus (oHSV), oncolytic adenovirus (oAd), measles virus (MV), vesicular stomatitis virus (VSV), zika virus (ZIKV), human telomerase reverse transcriptase (hTERT), transforming growth factor-beta receptor 2 fused with Fc protein (TGFβRIIFc), granulocyte–macrophage colony-stimulating factor (GM-CSF), Hypoxia-inducible factor-2α (HIF-2α), SRY-related HMG-box 10 (SOX10), epidermal growth factor receptor (EGFR)