Enzo Z. Poirier

Has grant

PSL Research University
Country flagFrance

Research Interests

Explore related searches

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

Recent Grants

Grant: Close

Understand and subvert the protective role of the aviD RNA interference pathway in physiology and cancer

Open Date: 2022-04-01

Close Date: 2025-03-01

Grant: Close

Stem cell immunity

Open Date: 2022-01-01

Close Date: 2025-12-01

Grant: Close

ATIP Avenir

Open Date: 2022-01-01

Close Date:

Grant: Close

ARN JCJC

Open Date: 2022-01-01

Close Date:

Grant: Close

Emergences Ville de Paris

Open Date: 2022-01-01

Close Date:

Articles (8)

Antiviral RNA interference (RNAi) is an immune pathway that can, in certain conditions, protect mammalian cells against RNA viruses. It depends on the recognition and dicing of viral double-stranded RNA by a protein of the Dicer family, which leads to the production of viral small interfering RNAs (vsiRNAs) that sequence-specifically guide the degradation of cognate viral RNA. If the first line of defence against viruses relies on type-I and type-III interferons (IFN) in mammals, certain cell types such as stem cells, that are hyporesponsive for IFN, instead use antiviral RNAi via the expression of a specific antiviral Dicer. In certain conditions, antiviral RNAi can also contribute to the protection of differentiated cells. Indeed, abundant vsiRNAs are detected in infected cells and efficiently guide the degradation of viral RNA, especially in cells infected with viruses disabled for viral suppressors of RNAi (VSRs), which are virally encoded blockers of antiviral RNAi. The existence and importance of antiviral RNAi in differentiated cells has however been debated in the field, because data document mutual inhibition between IFN and antiviral RNAi. Recent developments include the engineering of a small molecule inhibitor of VSR to probe antiviral RNAi in vivo, as well as the detection of vsiRNAs inside extracellular vesicles in the serum of infected mice. It suggests that using more complex, in vivo models could allow to unravel the contribution of antiviral RNAi to immunity at the host level.

Year:

2023

Year:

2023

Year:

2021

Year:

2021

Year:

2021

Year:

2020

Year:

2020

Year:

2020

Collaborators (17)

Jimena Perez-Lloret

University College London

UNITED KINGDOM
View details

Paula Ordonez

Teaching Fellow

Imperial College London

UNITED KINGDOM
View details

Johnathan Canton

Assistant Professor

University of Calgary

CANADA
View details

Nina Vora

University College London

UNITED KINGDOM
View details

James Fleming

Chief Information Officer

The Francis Crick Institute

UNITED KINGDOM
View details

Joshua Wright

-

NEW ZEALAND
View details

Margaret Crawford

The Francis Crick Institute

UNITED KINGDOM
View details

Rachel Ulferts

The Francis Crick Institute

UNITED KINGDOM
View details

Claudio Bussi

The Francis Crick Institute

UNITED KINGDOM
View details

Ellen Knuepfer

Lecturer

Royal Veterinary College - Hawkshead Campus

UNITED KINGDOM
View details

Graeme Hewitt

King’s College London

UNITED KINGDOM
View details

Neil Rogers

The Francis Crick Institute

UNITED KINGDOM
View details

Adam Sateriale

The Francis Crick Institute

UNITED KINGDOM
View details

Theo Sanderson

Assistant Professor

London School of Hygiene & Tropical Medicine

UNITED KINGDOM
View details

Amin Oomatia

University College London

UNITED KINGDOM
View details

Abhinay Ramaprasad

University of Glasgow

UNITED KINGDOM
View details

Caetano Reis e Sousa

The Francis Crick Institute

UNITED KINGDOM
View details
ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.