Dual-mechanism anti-CD73 antibodies CR201 and CR202 targeting distinct domains for cancer immunotherapy - Summary - MDSpire

Dual-mechanism anti-CD73 antibodies CR201 and CR202 targeting distinct domains for cancer immunotherapy

  • By

  • Miao Zhang

  • Haibin Yuan

  • Xindi Pan

  • Xian Li

  • Zichen Wang

  • Shuping Zhang

  • Zhigang Gu

  • Biao Hu

  • Xuedong Qu

  • Qian Wang

  • Xiangguo Gu

  • Bo Wang

  • Yu Cao

  • Guilin Mu

  • Guangbo Kang

  • Ario de Marco

  • Xiangshan Zhou

  • He Huang

  • June 10, 2026

  • 0 min

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Objective:

To develop novel anti-CD73 antibodies with dual mechanisms of action, including enzymatic blockade and receptor internalization, to disrupt the adenosine barrier in the tumor microenvironment.

Approach:
    Key Findings:
    • CR201 and CR202 bind to human and cynomolgus CD73, recognizing distinct structural domains, with CR202 targeting the N-terminal domain and CR201 targeting the C-terminal domain.
    • CR202 showed greater potency against membrane-bound CD73, while CR201 completely inhibited soluble CD73 activity.
    • Both antibodies restored T-cell proliferation and IFN-γ production and promoted CD73 internalization.
    • In vivo treatment with either antibody significantly suppressed tumor growth without observable toxicity.
    Interpretation:

    Limitations:
    • The study does not address potential long-term effects or the full range of immune responses.
    Conclusion:

    CR201 and CR202 represent next-generation therapeutic candidates for targeting the adenosine axis in cancer.

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