Completed Infection & Immunity Lungs & Breathing

Poxvirus immune evasion strategies.

In plain English

AI plain-English summary

Vaccinia virus, the weapon that eradicated smallpox, is still hiding tricks from the immune system, and this research will hunt them down. The problem is that even a successful vaccine leaves gaps in our understanding. Vaccinia virus (VACV) carries dozens of proteins that actively sabotage the host’s immune response, but many of these molecular weapons remain unidentified, and the mechanisms of known ones are poorly understood. This programme will systematically identify new VACV immune-evasion proteins, work out how they block host defences, and determine their three-dimensional structures. It will also investigate how host cells detect double-stranded DNA in the cytoplasm—a key alarm system for viral infection—and how VACV disables that alarm. This is fundamental science, not applied vaccine development. The immediate payoff is a deeper understanding of virus-host conflict at the molecular level. If successful, it will reveal the precise biochemical moves viruses use to win early battles against our cells. That knowledge could eventually guide the design of more immunogenic poxvirus-based vaccines or therapies for other viruses that use similar evasion tactics—but those applications are years away. For now, the value lies in mapping the battlefield.

View original technical description
This research programme will study the immune evasion strategies of vaccinia virus (VACV), the vaccine used to eradicate smallpox. The key goals are to i) identify new VACV proteins that interfere with the host response to infection, understand the mechanism of action of these proteins and what host molecules they interact with, and to evaluate the contribution these proteins make to virus virulence and immunogenicity; ii) further characterise VACV proteins that are known to interfere with the h ost response to infection and determine their structures alone and in combination with binding partners, and iii) identify and study the host molecules that sense dsDNA in the cytoplasm and to characterise VACV inhibitors of this(ese). Overall, this programme of work is designed to increase our knowledge of virus pathogenesis and the strategies viruses use to interfere with the host response to infection, to better understand the host innate response to infection, and to build more immunogenic p oxvirus based vaccines.

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Researchers

Geoffrey Smith (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Vaccinia virus entry, exit and evasion
Deciphering nanoscale interactions at the virus-host interface
Modulation of the Ubiquitin Proteasome System During Multiple Stages of the Poxvirus Lifecycle
Regulation of the dsDNA sensor protein-mediated anti-viral response by vaccinia virus
Restriction of DNA viruses by TRIM5a and ZAP / TRIM25 / KHNYN: mechanisms of restriction and viral evasion

Original classification

Principal Research Fellowship Renewal

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