Polymeric PD1/PDL1 bispecific antibody enhances immune checkpoint blockade therapy.

ABSTRACT: Immune checkpoint blockade (ICB) therapy, particularly PD1/PDL1 inhibition, has demonstrated success in bolstering durable responses in patients. However, the response rate remains below 30 %. In this study, we developed a polymeric bispecific antibody (BsAb) targeting PD1/PDL1 to enhance ICB therapy. Specifically, poly(_L-glutamic acid) (PGLU) was conjugated with a double cyclic Fc binding peptide, Fc-III-4C, through condensation reactions between the -COOH group of PGLU and the -NH₂ group of Fc-III-4C. This conjugate was then mixed with αPD1 and αPDL1 monoclonal antibodies (mAbs) in an aqueous solution. Mechanistically, the PD1/PDL1 BsAb (BsAb_αPD1+αPDL1) acts as a bridge between tumor cells and CD8⁺ T cells, continuously activating CD8⁺

SUBMITTER: Xue F 

PROVIDER: S-EPMC11421358 | biostudies-literature | 2024 Oct

REPOSITORIES: biostudies-literature