Development and Characterization of an Anti-Cancer Monoclonal Antibody for Treatment of Human Carcinomas.
Kwong Yok TsangMassimo FantiniSharon A MavroukakisAnjum ZakiChristina M AnnunziataPhilip M ArlenPublished in: Cancers (2022)
NEO-201 is an IgG1 humanized monoclonal antibody (mAb) that binds to tumor-associated variants of carcinoembryonic antigen-related cell adhesion molecule (CEACAM)-5 and CEACAM-6. NEO-201 reacts to colon, ovarian, pancreatic, non-small cell lung, head and neck, cervical, uterine and breast cancers, but is not reactive against most normal tissues. NEO-201 can kill tumor cells via antibody-dependent cell-mediated cytotoxicity (ADCC) and complement dependent cytotoxicity (CDC) to directly kill tumor cells expressing its target. We explored indirect mechanisms of its action that may enhance immune tumor killing. NEO-201 can block the interaction between CEACAM-5 expressed on tumor cells and CEACAM-1 expressed on natural killer (NK) cells to reverse CEACAM-1-dependent inhibition of NK cytotoxicity. Previous studies have demonstrated safety/tolerability in non-human primates, and in a first in human phase 1 clinical trial at the National Cancer Institute (NCI). In addition, preclinical studies have demonstrated that NEO-201 can bind to human regulatory T (Treg) cells. The specificity of NEO-201 in recognizing suppressive Treg cells provides the basis for combination cancer immunotherapy with checkpoint inhibitors targeting the PD-1/PD-L1 pathway.
Keyphrases
- monoclonal antibody
- endothelial cells
- clinical trial
- nk cells
- induced pluripotent stem cells
- induced apoptosis
- pluripotent stem cells
- gene expression
- stem cells
- cell cycle
- cell adhesion
- single cell
- cell therapy
- cell cycle arrest
- high grade
- open label
- dna damage
- cell proliferation
- bone marrow
- drug delivery
- study protocol
- genome wide
- case control
- dna methylation
- cancer therapy
- replacement therapy
- phase iii