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  • Assistant Professor
  • Associate Professor
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  • Full Professor
  • Honorary Professor
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  • Permanent Researcher
  • Pharmacist
  • PhD Student
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  • Post-doc
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  • Research Engineer
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  • Technician
  • Undergraduate Student
  • Veterinary
  • Visiting Scientist
  • Deputy Director of Center
  • Deputy Director of Department
  • Deputy Director of National Reference Center
  • Deputy Head of Facility
  • Director of Center
  • Director of Department
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© Research
Member: Head of Structure - Alumni

Sandra Pellegrini

Alumni

About

Sandra Pellegrini is Director of Research INSERM and Head of the Unit of Cytokine Signaling at the Institut Pasteur in Paris. After graduating with a Laurea in Biological Sciences at the University La Sapienza in Rome (Italy), she obtained a Ph.D in Basic Medical Sciences from New York University, New York (USA) in 1986. Following a post-doctoral training at the Imperial Cancer Research Fund, London (UK), she joined the Institut Pasteur. Since 2002, she heads a research unit in the Department of Immunology investigating molecular mechanisms underlying the pleiotropic action of type I interferons.

Projects

Project
Ongoing
3 Members

TYK2 variants in cytokine signaling and autoimmune diseases

Sandra Pellegrini (PI)

TYK2 belongs to the Janus/JAK family of protein tyrosine kinases and is involved in signaling of immunoregulatory cytokines (type I and type III IFNs, IL-6, IL-10 and IL-12 families) that contribute to a balanced […]
Project
Ongoing
2 Members

Exploring a link between ISGylation and cell cycle via SKP2

Sandra Pellegrini (PI)

We recently uncovered a potentially interesting connection between ISGylation and cell cycle regulation. We reported that the degradation of USP18, major negative regulator of IFN-I signaling, involves SKP2, a well known actor in cell […]
Project
Ongoing
2 Members

Fine-tuning of IFN-I response by USP18

Sandra Pellegrini (PI)

The type I IFN system needs to be regulated not only at the level of its production, but also at the level of responses. We have shown that cells that have responded to IFN-I […]

Publications

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