» Articles » PMID: 36335509

Covalently Conjugated NOD2/TLR7 Agonists Are Potent and Versatile Immune Potentiators

Overview
Journal J Med Chem
Specialty Chemistry
Date 2022 Nov 6
PMID 36335509
Authors
Affiliations
Soon will be listed here.
Abstract

The success of vaccination with subunit vaccines often relies on the careful choice of adjuvants. There is great interest in developing new adjuvants that can elicit a cellular immune response. Here, we address this challenge by taking advantage of the synergistic cross-talk between two pattern recognition receptors: nucleotide-binding oligomerization-domain-containing protein 2 (NOD2) and Toll-like receptor 7 (TLR7). We designed two conjugated NOD2/TLR7 agonists, which showed potent immunostimulatory activities in human primary peripheral blood mononuclear cells and murine bone-marrow-derived dendritic cells. One of these, , also generated a strong antigen-specific immune response , with a Th1-polarized profile. Importantly, our study shows that novel NOD2/TLR7 agonists elicit sophisticated and fine-tuned immune responses that are inaccessible to individual NOD2 and TLR7 agonists.

Citing Articles

Synthesis of Temporin-SHa Retro Analogs with Lysine Addition/Substitution and Antibiotic Conjugation to Enhance Antibacterial, Antifungal, and Anticancer Activities.

Nazir S, Khan A, Maharjan R, Khan S, Akram M, Maresca M Antibiotics (Basel). 2025; 13(12.

PMID: 39766603 PMC: 11672801. DOI: 10.3390/antibiotics13121213.


Linker Chemistry and Connectivity Fine-Tune the Immune Response and Kinetic Solubility of Conjugated NOD2/TLR7 Agonists.

Janez S, Guzelj S, Jakopin Z Bioconjug Chem. 2024; 35(11):1723-1731.

PMID: 39388220 PMC: 11583123. DOI: 10.1021/acs.bioconjchem.4c00321.


NOD2 reduces the chemoresistance of melanoma by inhibiting the TYMS/PLK1 signaling axis.

Yun F, Wu N, Yi X, Zhang X, Feng Y, Ni Q Cell Death Dis. 2024; 15(10):720.

PMID: 39353904 PMC: 11445241. DOI: 10.1038/s41419-024-07104-8.


Distinctive Immune Signatures Driven by Structural Alterations in Desmuramylpeptide NOD2 Agonists.

Janez S, Guzelj S, Kocbek P, de Vlieger E, Slutter B, Jakopin Z J Med Chem. 2024; 67(19):17585-17607.

PMID: 39344184 PMC: 11472310. DOI: 10.1021/acs.jmedchem.4c01577.


Synergistic Targeting of Innate Receptors TLR7 and NOD2 for Therapeutic Intervention in Multiple Sclerosis.

Dubik M, Marczynska-Grzelak J, Sorensen M, Dieu R, Rusin D, Schioth E Int J Mol Sci. 2024; 25(13).

PMID: 39000569 PMC: 11242768. DOI: 10.3390/ijms25137462.

References
1.
Underhill D . Collaboration between the innate immune receptors dectin-1, TLRs, and Nods. Immunol Rev. 2007; 219:75-87. DOI: 10.1111/j.1600-065X.2007.00548.x. View

2.
Griffith J, Sokol C, Luster A . Chemokines and chemokine receptors: positioning cells for host defense and immunity. Annu Rev Immunol. 2014; 32:659-702. DOI: 10.1146/annurev-immunol-032713-120145. View

3.
Malek T, Castro I . Interleukin-2 receptor signaling: at the interface between tolerance and immunity. Immunity. 2010; 33(2):153-65. PMC: 2946796. DOI: 10.1016/j.immuni.2010.08.004. View

4.
Guzelj S, Gobec M, Urbancic D, Mlinaric-Rascan I, Corsini E, Jakopin Z . Structural features and functional activities of benzimidazoles as NOD2 antagonists. Eur J Med Chem. 2020; 190:112089. DOI: 10.1016/j.ejmech.2020.112089. View

5.
Pierce S, Geanes E, Bradley T . Targeting Natural Killer Cells for Improved Immunity and Control of the Adaptive Immune Response. Front Cell Infect Microbiol. 2020; 10:231. PMC: 7248265. DOI: 10.3389/fcimb.2020.00231. View