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People who preserve immune resilience live longer, resist infections

People who preserve immune resilience live longer, resist infections
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People who preserve immune resilience live

An international team including researchers from The University of Texas Health Science Center at San Antonio have developed a novel set of metrics called "immune resilience" (IR) and shown that individuals with optimal levels of IR are more likely to live longer, resist HIV and influenza infections, and survive COVID-19 infections, among outcomes studied.

Mastering the Longevity Code: Immune Resilience Is Key to Resisting Disease and Living Longer

Multinational study identifies immune resilience as a factor that influences life span, HIV/AIDS, flu, sepsis mortality, recurrent skin cancer, and COVID-19 mortality. Researchers from The University of Texas Health Science Center at San Antonio, working with collaborators in five countries, toda

People who preserve immune resilience live

People who preserve immune resilience live
eurekalert.org - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from eurekalert.org Daily Mail and Mail on Sunday newspapers.

SARS-CoV-2 Mpro inhibitors with antiviral activity in a transgenic mouse model

The COVID-19 pandemic caused by the SARS-CoV-2 virus continually poses serious threats to global public health. The main protease (Mpro) of SARS-CoV-2 plays a central role in viral replication. We designed and synthesized 32 new bicycloproline-containing Mpro inhibitors derived from either Boceprevir or Telaprevir, both of which are approved antivirals. All compounds inhibited SARS-CoV-2 Mpro activity in vitro with IC50 values ranging from 7.6 to 748.5 nM. The co-crystal structure of Mpro in complex with MI-23, one of the most potent compounds, revealed its interaction mode. Two compounds (MI-09 and MI-30) showed excellent antiviral activity in cell-based assays. In a SARS-CoV-2 infection transgenic mouse model, oral or intraperitoneal treatment with MI-09 or MI-30 significantly reduced lung viral loads and lung lesions. Both also displayed good pharmacokinetic properties and safety in rats.

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