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Combination strategies with PD-1/PD-L1 blockade: current advances and future directions

📅 January 21, 2022 👤 Ming Yi, Xiaoli Zheng, Mengke Niu et al. 📖 Molecular Cancer 📊 1,443 citations

🤖 Plain-English Summary

Antibodies targeting programmed cell death protein-1 (PD-1) or its ligand PD-L1 rescue T cells from exhausted status and revive immune response against cancer cells. Moreover, we focused on the advances of α-PD-1/PD-L1-based immunomodulatory strategies in clinical studies.

🔑 Key Findings

  • Based on the immense success in clinical trials, ten α-PD-1 (nivolumab, pembrolizumab, cemiplimab, sintilimab, camrelizumab, toripalimab, tislelizumab, zimberelimab, prolgolimab, and dostarlimab) and three α-PD-L1 antibodies (atezolizumab, durvalumab, and avelumab) have been approved for various types of cancers.
  • Nevertheless, the low response rate of α-PD-1/PD-L1 therapy remains to be resolved.
  • For most cancer patients, PD-1/PD-L1 pathway is not the sole speed-limiting factor of antitumor immunity, and it is insufficient to motivate effective antitumor immune response by blocking PD-1/PD-L1 axis.

💡 Why This Matters

These innovations can translate to real-world improvements in technology, infrastructure, and everyday tools.

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📋 Article Details

Category ⚙️ Engineering & Technology
Published Jan 21, 2022
Journal Molecular Cancer
Authors Ming Yi, Xiaoli Zheng, Mengke Niu, Shuangli Zhu, Hong Ge
DOI 10.1186/s12943-021-01489-2
Citations 1,443
Source OpenAlex

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