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Table 4 Other combination of chemotherapy drugs and immunotherapy agents

From: Nanoparticle-mediated synergistic chemoimmunotherapy for tailoring cancer therapy: recent advances and perspectives

Carrier design (Structure/Injection route)

Chemotherapy agent

Immunotherapy agents

Tumor type

Synergic actions and advantages of NPs in the combination

Refs.

Lipid NPs (Pegylated liposome/IV)

DOX

Alendronate

Female Balb/C and Sabra tumor models

High loading efficiency of DOX and increased stability in biological fluids

More potent activation of the inflammasome pathway leading to 40-fold greater secretion of IL-1β

High therapeutic efficacy due to synergy of alendronate and DOX

[170]

(Hydrogel/SC)

Melittin-RADA32

Melanoma

Considerable tumor inhibition with the activated NK cells recruitment in the tumors

Regulation of innate immune cells, direct anti-cancer and immune-stimulating capabilities

Activation of DCs of draining lymph nodes, production of CTLs, and depletion of M2-like TAMs

[171]

(pH-sensitive smart nanocubes/IV)

pOVA vaccine

Melanoma, MQ model and lung carcinoma

Higher anti-tumor efficacy, longer survival rates, and increased tumor inhibition ratio compared to monotherapy

Higher OVA protein production

Provoking humoral immunity after a single injection and significant humoral immunogenic memory production

[172]

Polymeric NPs (Polymerized β-cyclodextrin/Intratumoral)

PTX

NO

Melanoma, mammary carcinoma, lymphoma and colon carcinoma

Synergistic cytotoxicity and induction of ICD on tumor cells

Activation and expansion of DCs leading to expansion of CTLs

[173]

(Dual-pH-sensitive micelle system /Tail vein)

LXR agonist RGX-104

Breast cancer

Significant tumor accumulation, as well as tumor growth suppression

Reducing immunosuppressive MDSCs levels and increasing infiltration and anti-tumor effect of CTLs

Effective increase in expression of ApoE in tumor tissues

Suppression of TGF-β and IL-10 production and enhancement of the number of CD4+ and CD8+ T cells

[174]

Hybrid NPs (HA coated cationic albumin NPs/Tail vein)

Celastrol

IDO inhibitor, 1-methyltryptophan

Pancreatic cancer

Increase in cytotoxicity, apoptosis induction, and tumor inhibition

Downregulation of the immunosuppressive TME through upregulating CD4+ T cells in the spleen

[175]

Nanogel (Folated pH-degradable PVA/Tail vein)

DTX

IDO1 inhibitor, NLG919

Breast cancer

Increased intratumoral infiltration of CTLs and NK cells and inhibition of MDSCs infiltration

Regulation of IDO1-mediated immunosuppressive TME

[136]

Lipid NPs (Liposome/IV)

DOX

IDO1 inhibitor, Indoximod

Metastatic breast cancer

Significant increase in anti-breast cancer immune response

Remarkable tumor cell elimination at the primary tumor sites, as well as metastatic sites

Activation of CTLs, depletion of Tregs, and enhancement in CD8+/FOXP3+ T cell ratios

Less toxicity in liver, heart, and kidney compared to free DOX

(176)

  1. HA hyaluronic acid, PVA polyvinyl alcohol, LXR liver-X nuclear receptor, pOVA plasmid ovalbumin, NO nitric oxide