Polymer-based antibody mimetics (iBodies) target human PD-L1 and function as a potent immune checkpoint blocker
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
38685532
PubMed Central
PMC11154707
DOI
10.1016/j.jbc.2024.107325
PII: S0021-9258(24)01826-X
Knihovny.cz E-zdroje
- Klíčová slova
- HPMA copolymer, PD-1, PD-L1, T-cell, antibody mimetic, immune checkpoint, immunosuppression, immunotherapy, inhibitor, tumor immunology,
- MeSH
- antigeny CD274 * antagonisté a inhibitory imunologie metabolismus MeSH
- inhibitory kontrolních bodů * farmakologie chemie MeSH
- lidé MeSH
- monoklonální protilátky chemie farmakologie MeSH
- nádorové buněčné linie MeSH
- polymery chemie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antigeny CD274 * MeSH
- CD274 protein, human MeSH Prohlížeč
- inhibitory kontrolních bodů * MeSH
- monoklonální protilátky MeSH
- polymery MeSH
Immune checkpoint blockade (ICB) using monoclonal antibodies against programmed cell death protein 1 (PD-1) or programmed death-ligand 1 (PD-L1) is the treatment of choice for cancer immunotherapy. However, low tissue permeability, immunogenicity, immune-related adverse effects, and high cost could be possibly improved using alternative approaches. On the other hand, synthetic low-molecular-weight (LMW) PD-1/PD-L1 blockers have failed to progress beyond in vitro studies, mostly due to low binding affinity or poor pharmacological characteristics resulting from their limited solubility and/or stability. Here, we report the development of polymer-based anti-human PD-L1 antibody mimetics (α-hPD-L1 iBodies) by attaching the macrocyclic peptide WL12 to a N-(2-hydroxypropyl)methacrylamide copolymer. We characterized the binding properties of iBodies using surface plasmon resonance, enzyme-linked immunosorbent assay, flow cytometry, confocal microscopy, and a cellular ICB model. We found that the α-hPD-L1 iBodies specifically target human PD-L1 (hPD-L1) and block the PD-1/PD-L1 interaction in vitro, comparable to the atezolizumab, durvalumab, and avelumab licensed monoclonal antibodies targeting PD-L1. Our findings suggest that iBodies can be used as experimental tools to target hPD-L1 and could serve as a platform to potentiate the therapeutic effect of hPD-L1-targeting small molecules by improving their affinity and pharmacokinetic properties.
Centre d'Immunologie de Marseille Luminy Aix Marseille Université INSERM CNRS Marseille France
Institute of Organic Chemistry and Biochemistry Czech Academy of Sciences Prague Czech Republic
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