Discovery of Anti-PD-L1 Human Domain Antibodies for Cancer Immunotherapy

Immunotherapy using monoclonal antibodies targeting the PD-1/PD-L1 interaction has shown enormous success for various cancers. Despite their encouraging results in clinics, antibody-based checkpoint inhibitors have several limitations, such as poor tumor penetration. To address these limitations of monoclonal antibodies, there is a growing interest in developing low-molecular-weight checkpoint inhibitors, such as antibody fragments. Several antibody fragments targeting PD-1/PD-L1 were recently discovered using phage libraries from camel or alpaca. However, animal-derived antibody fragments may elicit unwanted immune responses, which limit their therapeutic applications. For the first time, we used a human domain antibody phage library and discovered anti-human PD-L1 human single-domain antibodies (dAbs) that block the PD-1/PD-L1 interaction. Among them, the CLV3 dAb shows the highest affinity to PD-L1. The CLV3 dAb also exhibits the highest blocking efficacy of the PD-1/PD-L1 interaction. Moreover, the CLV3 dAb significantly inhibits tumor growth in mice implanted with CT26 colon carcinoma cells. These results suggest that CLV3 dAb can be potentially used as an anti-PD-L1 inhibitor for cancer immunotherapy.

Automated summary

This study discovered anti-human PD-L1 single-domain antibodies (dAbs) that block the PD-1/PD-L1 interaction using a human domain antibody phage library for the first time. Among them, the CLV3 dAb showed the highest affinity and blocking efficacy to PD-L1, and significantly inhibited tumor growth in mice. These results suggest the potential of CLV3 dAb as an anti-PD-L1 inhibitor for cancer immunotherapy.