JinHuangJieDu (JHJD) formula attenuates SARS-CoV-2 infection by interrupting RBD-ACE2 binding and HIF-1α-dependent inflammation - Summary - MDSpire

JinHuangJieDu (JHJD) formula attenuates SARS-CoV-2 infection by interrupting RBD-ACE2 binding and HIF-1α-dependent inflammation

  • By

  • Zhan-Qun Yang

  • Ning Ding

  • Meng-Zhu Zheng

  • Jian Wen

  • Yuan Xue

  • Li-Ting Zheng

  • Yi-Heng Yang

  • Cheng-He Shi

  • Hua Jiang

  • Jian Lin

  • Long Chen

  • May 11, 2026

  • 0 min

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Objective:

To evaluate the therapeutic potential and mechanism of action of the JinHuangJieDu (JHJD) formula against SARS-CoV-2, highlighting its relevance in current treatment strategies.

Key Findings:
  • JHJD effectively blocked wildtype and Omicron RBD binding to ACE2, suggesting its potential as a therapeutic agent.
  • Inhibition of pseudovirus infection was observed, indicating a direct antiviral effect.
  • Network analyses identified 375 ingredients, 338 targets, and 63 significant pathways, providing a comprehensive overview of JHJD's action.
  • CCND1 and HIF1A were identified as pivotal genes, linking JHJD's effects to critical biological processes.
  • JHJD targets HIF-1α to attenuate inflammation, which may improve patient outcomes.
Interpretation:

JHJD demonstrates dual mechanisms of action by disrupting the RBD-ACE2 interaction and modulating inflammation, making it a promising therapeutic candidate for COVID-19, particularly in light of emerging variants.

Limitations:
  • The study primarily focused on in vitro assessments; clinical efficacy remains to be established, necessitating further clinical trials.
  • Further studies are needed to explore the long-term effects and safety of JHJD, which are crucial for its potential use in clinical settings.
Conclusion:

JHJD is a novel TCM formula that shows potential in inhibiting SARS-CoV-2 entry and alleviating inflammation, particularly effective against Omicron variants, warranting further investigation in clinical trials.

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