Multicyclic Peptides Targeting PD-L1 for Radiotheranostics: From Discovery to Clinical Proof-of-Concept

Radiotheranostics holds transformative potential for precision oncology by integrating diagnostic imaging with targeted radionuclide therapy. However, advancements in this field are significantly hindered by the limited availability of high-affinity ligands that are capable of engaging challenging cell-surface antigens, particularly flat, low-druggability targets such as programmed death-ligand 1 (PD-L1). Here, we overcome this barrier through de novo discovery and rational engineering of a disulfide-directed multicyclic peptide (DDMP), dmp10, which achieves a picomolar affinity for PD-L1 by leveraging conformationally constrained structural scaffolds. By combining disulfide-directed library design with iterative directed evolution, we successfully generated dmp10, a ∼3 kDa multicyclic peptide that establishes unprecedented shape complementarity to the expansive binding interface of PD-L1. Preclinical evaluations demonstrated that <sup>68</sup>Ga-labeled dmp10 enables high-contrast PET imaging of PD-L1<sup>+</sup> tumors in murine models, achieving a tumor uptake of 13.27 %ID/g at 4 h post-injection. The therapeutic counterpart, <sup>177</sup>Lu-labeled dmp10, effectively eradicated 92.47% of established tumors in tumor models while sparing healthy tissues, thereby validating its dual radiotheranostic utility. The translational relevance of our findings was further confirmed in a first-in-human pilot study, where <sup>68</sup>Ga-labeled dmp10 was well tolerated and allowed visualization of PD-L1<sup>+</sup> lesions in patients with solid tumors. This work not only establishes DDMPs as a versatile platform for targeting geometrically complex antigens but also delivers a promising radiotheranostic agent that bridges molecular imaging and precision radionuclide therapy for PD-L1-driven malignancies. Our findings advance current strategies for designing ultrahigh-affinity peptide binders and underscore the untapped potential of multicyclic architectures in overcoming longstanding challenges in cancer theranostics.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2025-09-20
DOI
https://doi.org/10.1021/jacs.5c11292
Citations
8
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
8.36
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article

Multicyclic Peptides Targeting PD-L1 for Radiotheranostics: From Discovery to Clinical Proof-of-Concept

Shihui Fan, Meirong Chen, Chaoying Xu, Yibei Xiao et al.
8 citations
Journal of the American Chemical Society
Cancer Immunotherapy and Biomarkers
8.36
article

Multicyclic Peptides Targeting PD-L1 for Radiotheranostics: From Discovery to Clinical Proof-of-Concept

Shihui Fan, Meirong Chen, Chaoying Xu, Yibei Xiao, Jie Zhuang, Xin Gao, Qingshuang Lu, Hongtan Liu, Chuanliu Wu, Xueyao Chen, Rui Wang, Bin Lin, Naixin Liang, Shuo Jiang, Yang Pan, Zhaohui Zhu, Xueting Cheng, X.-G. Peng, Kuan Hu, Siqi Zhang
article en
8 citations

Abstract

Radiotheranostics holds transformative potential for precision oncology by integrating diagnostic imaging with targeted radionuclide therapy. However, advancements in this field are significantly hindered by the limited availability of high-affinity ligands that are capable of engaging challenging cell-surface antigens, particularly flat, low-druggability targets such as programmed death-ligand 1 (PD-L1). Here, we overcome this barrier through de novo discovery and rational engineering of a disulfide-directed multicyclic peptide (DDMP), dmp10, which achieves a picomolar affinity for PD-L1 by leveraging conformationally constrained structural scaffolds. By combining disulfide-directed library design with iterative directed evolution, we successfully generated dmp10, a ∼3 kDa multicyclic peptide that establishes unprecedented shape complementarity to the expansive binding interface of PD-L1. Preclinical evaluations demonstrated that <sup>68</sup>Ga-labeled dmp10 enables high-contrast PET imaging of PD-L1<sup>+</sup> tumors in murine models, achieving a tumor uptake of 13.27 %ID/g at 4 h post-injection. The therapeutic counterpart, <sup>177</sup>Lu-labeled dmp10, effectively eradicated 92.47% of established tumors in tumor models while sparing healthy tissues, thereby validating its dual radiotheranostic utility. The translational relevance of our findings was further confirmed in a first-in-human pilot study, where <sup>68</sup>Ga-labeled dmp10 was well tolerated and allowed visualization of PD-L1<sup>+</sup> lesions in patients with solid tumors. This work not only establishes DDMPs as a versatile platform for targeting geometrically complex antigens but also delivers a promising radiotheranostic agent that bridges molecular imaging and precision radionuclide therapy for PD-L1-driven malignancies. Our findings advance current strategies for designing ultrahigh-affinity peptide binders and underscore the untapped potential of multicyclic architectures in overcoming longstanding challenges in cancer theranostics.

Journal of the American Chemical SocietyVol. 147(39)
Academy of Medical Sciences (GB), China Pharmaceutical University (CN), Xiamen University (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), State Administration of Traditional Chinese Medicine of the People's Republic of China (CN), Peking Union Medical College Hospital (CN), Shanghai Institute of Materia Medica (CN), Collaborative Innovation Center of Chemistry for Energy Materials (CN)
Openalex Percentile: Top 2%
Cancer Immunotherapy and Biomarkers
8.36
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