Gold Glyconanoparticles Combined with 91-99 Peptide of the Bacterial Toxin, Listeriolysin O, Are Efficient Immunotherapies in Experimental Bladder Tumors.
Hector Terán-NavarroAndrea ZeoliDavid Salines-CuevasMarco MarradiNoemi MontoyaElena GonzálezJavier Gonzalo Ocejo-VinyalsMario Dominguez-EstebanJose Luis Gutierrez-BañosFelix Campos-JuanateySonsoles Yañez-DiazAlmudena Garcia-CastañoFernando RiveraIgnacio DuranCarmen Alvarez-DominguezPublished in: Cancers (2022)
This study presents proof of concept assays to validate gold nanoparticles loaded with the bacterial peptide 91-99 of the listeriolysin O toxin (GNP-LLO 91-99 nanovaccines) as immunotherapy for bladder tumors. GNP-LLO 91-99 nanovaccines showed adjuvant abilities as they induce maturation and activation of monocyte-derived dendritic cells (MoDCs) to functional antigen-presenting cells in healthy donors and patients with melanoma or bladder cancer (BC), promoting a Th1 cytokine pattern. GNP-LLO 91-99 nanovaccines were also efficient dendritic cell inducers of immunogenic tumor death using different bladder and melanoma tumor cell lines. The establishment of a pre-clinical mice model of subcutaneous BC confirmed that a single dose of GNP-LLO 91-99 nanovaccines reduced tumor burden 4.7-fold and stimulated systemic Th1-type immune responses. Proof of concept assays validated GNP-LLO 91-99 nanovaccines as immunotherapy by comparison to anti-CTLA-4 or anti-PD-1 antibodies. In fact, GNP-LLO 91-99 nanovaccines increased percentages of CD4 + and CD8 + T cells, B cells, and functional antigen-presenting DCs in tumor-infiltrated lymphocytes, while they reduced the levels of myeloid-derived suppressor cells (MDSC) and suppressor T cells (T reg ). We conclude that GNP-LLO 91-99 nanovaccines can work as monotherapies or combinatory immunotherapies with anti-CTLA-4 or anti-PD-1 antibodies for solid tumors with high T cell infiltration, such as bladder cancer or melanoma.
Keyphrases
- dendritic cells
- immune response
- gold nanoparticles
- induced apoptosis
- spinal cord injury
- escherichia coli
- cell cycle arrest
- regulatory t cells
- case report
- peripheral blood
- early stage
- type diabetes
- toll like receptor
- adipose tissue
- endothelial cells
- skeletal muscle
- endoplasmic reticulum stress
- reduced graphene oxide
- signaling pathway
- urinary tract
- basal cell carcinoma
- pi k akt
- clinical evaluation