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Structural and biological characterization of pAC65, a macrocyclic peptide that blocks PD-L1 with equivalent potency to the FDA-approved antibodies

Recent advances in immuno-oncology have opened up new and impressive treatment options for cancer. Notwithstanding, overcoming the limitations of the current FDA-approved therapies with monoclonal antibodies (mAbs) that block the PD-1/PD-L1 pathway continues to lead to the testing of multiple approa...

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Published in:Molecular cancer 2023-09, Vol.22 (1), p.1-150, Article 150
Main Authors: Rodriguez, Ismael, Kocik-Krol, Justyna, Skalniak, Lukasz, Musielak, Bogdan, Wisniewska, Aneta, CiesioÅkiewicz, Agnieszka, Berlicki, Åukasz, Plewka, Jacek, Grudnik, Przemyslaw, Stec, Malgorzata, Siedlar, Maciej, Holak, Tad A, Magiera-Mularz, Katarzyna
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container_title Molecular cancer
container_volume 22
creator Rodriguez, Ismael
Kocik-Krol, Justyna
Skalniak, Lukasz
Musielak, Bogdan
Wisniewska, Aneta
CiesioÅkiewicz, Agnieszka
Berlicki, Åukasz
Plewka, Jacek
Grudnik, Przemyslaw
Stec, Malgorzata
Siedlar, Maciej
Holak, Tad A
Magiera-Mularz, Katarzyna
description Recent advances in immuno-oncology have opened up new and impressive treatment options for cancer. Notwithstanding, overcoming the limitations of the current FDA-approved therapies with monoclonal antibodies (mAbs) that block the PD-1/PD-L1 pathway continues to lead to the testing of multiple approaches and optimizations. Recently, a series of macrocyclic peptides have been developed that exhibit binding strengths to PD-L1 ranging from sub-micromolar to micromolar. In this study, we present the most potent non-antibody-based PD-1/PD-L1 interaction inhibitor reported to date. The structural and biological characterization of this macrocyclic PD-L1 targeting peptide provides the rationale for inhibition of both PD-1/PD-L1 and CD80/PD-L1 complexes. The IC50 and EC50 values obtained in PD-L1 binding assays indicate that the pAC65 peptide has potency equivalent to the current FDA-approved mAbs and may have similar activity to the BMS986189 peptide, which entered the clinical trial and has favorable safety and pharmacokinetic data. The data presented here delineate the generation of similar peptides with improved biological activities and applications not only in the field of cancer immunotherapy but also in other disorders related to the immune system.
doi_str_mv 10.1186/s12943-023-01853-4
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source Open Access: PubMed Central; Publicly Available Content Database
subjects Antibodies
Biological products
Cancer
Cancer immunotherapy
CD80
CD80 antigen
Correspondence
Drug approval
Hydrogen bonds
Immune checkpoint blockade
Immune system
Immunotherapy
Ligands
Lymphocytes
Monoclonal antibodies
PD-1
PD-1 protein
PD-L1
PD-L1 protein
Peptides
Pharmacokinetics
Programmed death 1
Programmed death ligand 1
Proteins
title Structural and biological characterization of pAC65, a macrocyclic peptide that blocks PD-L1 with equivalent potency to the FDA-approved antibodies
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