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Eric Perouzel
Researcher at Imperial College London
Publications - 41
Citations - 1343
Eric Perouzel is an academic researcher from Imperial College London. The author has contributed to research in topics: Liposome & Immune system. The author has an hindex of 21, co-authored 40 publications receiving 1130 citations. Previous affiliations of Eric Perouzel include Mitsubishi.
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Journal ArticleDOI
Dectin-1 Is Essential for Reverse Transcytosis of Glycosylated SIgA-Antigen Complexes by Intestinal M Cells
Nicolas Rochereau,Daniel Drocourt,Eric Perouzel,Vincent Pavot,Pierre Redelinghuys,Gordon D. Brown,Gérard Tiraby,Xavier Roblin,Bernard Verrier,Christian Genin,Blaise Corthésy,Stéphane Paul +11 more
TL;DR: This work reports the long-awaited identification of Dectin-1 and Siglec-5 as the M cell co-receptors that mediate the reverse transcytosis of secretory IgA molecules to mount a gut immune response.
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Encapsulation of Nod1 and Nod2 receptor ligands into poly(lactic acid) nanoparticles potentiates their immune properties
Vincent Pavot,Nicolas Rochereau,Charlotte Primard,Christian Genin,Eric Perouzel,Thierry Lioux,Stéphane Paul,Bernard Verrier +7 more
TL;DR: Co-injection of encapsulated Nod-ligands with PLA particles carrying Gag p24 HIV-1 antigen allowed a 100 fold increase in antibody responses in comparison to Alum.
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Rational design of adjuvants targeting the C-type lectin Mincle.
Alexiane Decout,Sandro Silva-Gomes,Daniel Drocourt,Sophie Barbe,Isabelle André,Francisco J. Cueto,Thierry Lioux,David Sancho,Eric Perouzel,Alain Vercellone,Jacques Prandi,Martine Gilleron,Gérard Tiraby,Jérôme Nigou +13 more
TL;DR: New compounds inducing stronger immune responses than the currently available Mincle ligands that represent new powerful adjuvant molecules are synthesized and found to induce strong Th1 and Th17 immune responses in vivo in immunization experiments in mice and conferred protection in a murine model of Mycobacteria tuberculosis infection.
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Characterisation of LMD virus-like nanoparticles self-assembled from cationic liposomes, adenovirus core peptide μ (mu) and plasmid DNA
Toshiaki Tagawa,Michelle C Manvell,Nick Brown,Michael D. Keller,Eric Perouzel,Karl Murray,Richard P. Harbottle,M. Tecle,F. Booy,M C Brahimi-Horn,Charles Coutelle,Nicholas R. Lemoine,Eric W.F.W. Alton,Andrew D. Miller +13 more
TL;DR: LMD particles can be formulated reproducibly, they are amenable to long-term storage at −80°C and are stable to aggregation at a plasmid DNA concentration up to 5 mg/ml, which make LMD an important new non-viral vector platform system from which to derive tailor-made non-Viral delivery systems by a process of systematic modular upgrading.
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Nuclear localisation sequence templated nonviral gene delivery vectors: investigation of intracellular trafficking events of LMD and LD vector systems.
Michael D. Keller,Richard P. Harbottle,Eric Perouzel,Morvane Colin,Imran Shah,Ahad A. Rahim,Laurence Vaysse,Anna Bergau,S Moritz,Christiane Brahimi-Horn,Charles Coutelle,Andrew D. Miller +11 more
TL;DR: LD systems prepared from DC‐Chol/DOPE cationic liposomes and pDNA(Cy3) behave similarly to LMD systems, which suggests that mu peptide is unable to influence trafficking events in this current LMD formulation, in spite of its strong NLS capacity.