Skip to main content
ukiyo journal - 日本と世界をつなぐ新しいニュースメディア Logo
  • All Articles
  • 🗒️ Register
  • 🔑 Login
    • 日本語
    • 中文
    • Español
    • Français
    • 한국어
    • Deutsch
    • ภาษาไทย
    • हिंदी
Cookie Usage

We use cookies to improve our services and optimize user experience. Privacy Policy and Cookie Policy for more information.

Cookie Settings

You can configure detailed settings for cookie usage.

Essential Cookies

Cookies necessary for basic site functionality. These cannot be disabled.

Analytics Cookies

Cookies used to analyze site usage and improve our services.

Marketing Cookies

Cookies used to display personalized advertisements.

Functional Cookies

Cookies that provide functionality such as user settings and language selection.

New Coronavirus: "Possibly Effective Against All Variants"? The Key to Overcoming Mutations Lies in "Humans" — RIKEN and Others Take the Next Step with TMPRSS2 Antibodies

New Coronavirus: "Possibly Effective Against All Variants"? The Key to Overcoming Mutations Lies in "Humans" — RIKEN and Others Take the Next Step with TMPRSS2 Antibodies

2025年09月13日 00:57
On September 11, 2025, a collaborative research group from RIKEN, the Institute of Medical Science at the University of Tokyo, and Shiga University of Medical Science announced the development of a monoclonal antibody targeting the human enzyme TMPRSS2, which is essential for SARS-CoV-2 infection. This antibody was shown to suppress infection across all examined variants, including Omicron. Notably, the antibody does not inhibit the enzymatic activity of TMPRSS2 itself but physically disrupts the interaction among spike, ACE2, and TMPRSS2. The effectiveness of both prophylactic and therapeutic administration was suggested in human lung organoids, mice, and cynomolgus monkeys. The findings were published in iScience. On social media, there are voices of optimism, calling it "Nobel Prize-worthy," alongside cautious remarks pointing out that safety and efficacy have not yet been verified in preclinical stages. It is crucial to carefully assess the reproducibility in clinical trials, the emergence of alternative entry pathways (endosome/MMP), and implementation challenges such as administration routes and costs.
← Back to Article List

Contact |  Terms of Service |  Privacy Policy |  Cookie Policy |  Cookie Settings

© Copyright ukiyo journal - 日本と世界をつなぐ新しいニュースメディア All rights reserved.