tetano
Editor, Senior Moderator
MedComm (2020)
. 2024 Jul 28;5(8):e666.
doi: 10.1002/mco2.666. eCollection 2024 Aug. Development of potent pan-coronavirus fusion inhibitors with a new design strategy
Yuanmei Zhu[SUP] 1 [/SUP], Zhongcai Gao[SUP] 2 [/SUP], Xiaoli Feng[SUP] 3 [/SUP], Lin Cheng[SUP] 4 [/SUP], Nian Liu[SUP] 1 [/SUP], Chao Liu[SUP] 2 [/SUP], Shaowei Han[SUP] 2 [/SUP], Qiaojiang Yang[SUP] 3 [/SUP], Qingcui Zou[SUP] 3 [/SUP], Huihui Chong[SUP] 1 [/SUP], Zheng Zhang[SUP] 4 [/SUP], Minghua Li[SUP] 3 [/SUP], Gengshen Song[SUP] 2 [/SUP], Yuxian He[SUP] 1 [/SUP]
Affiliations
Development of potent and broad-spectrum drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) remains one of the top priorities, especially in the cases of the emergence of mutant viruses and inability of current vaccines to prevent viral transmission. In this study, we have generated a novel membrane fusion-inhibitory lipopeptide IPB29, which is currently under clinical trials; herein, we report its design strategy and preclinical data. First, we surprisingly found that IPB29 with a rigid linker between the peptide sequence and lipid molecule had greatly improved α-helical structure and antiviral activity. Second, IPB29 potently inhibited a large panel of SARS-CoV-2 variants including the previously and currently circulating viruses, such as Omicron XBB.5.1 and EG.5.1. Third, IPB29 could also cross-neutralize the bat- and pangolin-isolated SARS-CoV-2-related CoVs (RatG13, PCoV-GD, and PCoV-GX) and other human CoVs (SARS-CoV, MERS-CoV, HCoV-NL63, and HCoV-229E). Fourth, IPB29 administrated as an inhalation solution (IPB29-IS) in Syrian hamsters exhibited high therapeutic and preventive efficacies against SARS-CoV-2 Delta or Omicron variant. Fifth, the pharmacokinetic profiles and safety pharmacology of IPB29-IS were extensively characterized, providing data to support its evaluation in humans. In conclusion, our studies have demonstrated a novel design strategy for viral fusion inhibitors and offered an ideal drug candidate against SARS-CoV-2 and other coronaviruses.
Keywords: SARS‐CoV‐2; coronavirus; fusion inhibitor; lipopeptide.
. 2024 Jul 28;5(8):e666.
doi: 10.1002/mco2.666. eCollection 2024 Aug. Development of potent pan-coronavirus fusion inhibitors with a new design strategy
Yuanmei Zhu[SUP] 1 [/SUP], Zhongcai Gao[SUP] 2 [/SUP], Xiaoli Feng[SUP] 3 [/SUP], Lin Cheng[SUP] 4 [/SUP], Nian Liu[SUP] 1 [/SUP], Chao Liu[SUP] 2 [/SUP], Shaowei Han[SUP] 2 [/SUP], Qiaojiang Yang[SUP] 3 [/SUP], Qingcui Zou[SUP] 3 [/SUP], Huihui Chong[SUP] 1 [/SUP], Zheng Zhang[SUP] 4 [/SUP], Minghua Li[SUP] 3 [/SUP], Gengshen Song[SUP] 2 [/SUP], Yuxian He[SUP] 1 [/SUP]
Affiliations
- PMID: 39070180
- PMCID: PMC11283584
- DOI: 10.1002/mco2.666
Development of potent and broad-spectrum drugs against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) remains one of the top priorities, especially in the cases of the emergence of mutant viruses and inability of current vaccines to prevent viral transmission. In this study, we have generated a novel membrane fusion-inhibitory lipopeptide IPB29, which is currently under clinical trials; herein, we report its design strategy and preclinical data. First, we surprisingly found that IPB29 with a rigid linker between the peptide sequence and lipid molecule had greatly improved α-helical structure and antiviral activity. Second, IPB29 potently inhibited a large panel of SARS-CoV-2 variants including the previously and currently circulating viruses, such as Omicron XBB.5.1 and EG.5.1. Third, IPB29 could also cross-neutralize the bat- and pangolin-isolated SARS-CoV-2-related CoVs (RatG13, PCoV-GD, and PCoV-GX) and other human CoVs (SARS-CoV, MERS-CoV, HCoV-NL63, and HCoV-229E). Fourth, IPB29 administrated as an inhalation solution (IPB29-IS) in Syrian hamsters exhibited high therapeutic and preventive efficacies against SARS-CoV-2 Delta or Omicron variant. Fifth, the pharmacokinetic profiles and safety pharmacology of IPB29-IS were extensively characterized, providing data to support its evaluation in humans. In conclusion, our studies have demonstrated a novel design strategy for viral fusion inhibitors and offered an ideal drug candidate against SARS-CoV-2 and other coronaviruses.
Keywords: SARS‐CoV‐2; coronavirus; fusion inhibitor; lipopeptide.