E
Edward J. Pearce
Researcher at Max Planck Society
Publications - 237
Citations - 34759
Edward J. Pearce is an academic researcher from Max Planck Society. The author has contributed to research in topics: Schistosoma mansoni & Immune system. The author has an hindex of 81, co-authored 218 publications receiving 30184 citations. Previous affiliations of Edward J. Pearce include National Institutes of Health & Ithaca College.
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Journal ArticleDOI
Schistosoma mansoni infection-induced transcriptional changes in hepatic macrophage metabolism correlate with an athero-protective phenotype
Diana Cortes-Selva,Andrew Elvington,Andrew Elvington,Andrew Ready,Bartek Rajwa,Edward J. Pearce,Gwendalyn J. Randolph,Keke C. Fairfax,Keke C. Fairfax +8 more
TL;DR: The results suggest a previously unknown and unreported role of hepatic macrophages in the modulation of whole body lipid and glucose metabolism during infection and provide a template for examining the role of immunomodulation on the long-term metabolism of the host.
Journal ArticleDOI
Reverse genetics and the study of the immune response to schistosomes.
Edward J. Pearce,Tori C. Freitas +1 more
TL;DR: Recent advances in the development of tools for studying gene function in schistosomes are reviewed and how these new tools may be exploited to investigate issues of key importance in the interaction of schistOSomes with the host immune system are discussed.
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Plasmacytoid dendritic cell activation is dependent on coordinated expression of distinct amino acid transporters
Katarzyna M. Grzes,David E. Sanin,David E. Sanin,Agnieszka M. Kabat,Michal A. Stanczak,Michal A. Stanczak,Joy Edwards-Hicks,Mai Matsushita,Alexandra Hackl,Fabian Hässler,Kristin Knoke,Sophie Zahalka,Matteo Villa,David M. Kofler,Reinhard E. Voll,Paola Zigrino,Mario Fabri,Erika L. Pearce,Edward J. Pearce +18 more
TL;DR: This article found that IL-3-induced Janus kinase 2-dependent expression of SLC7A5 and SLC3A2 was required for mammalian target of rapamycin complex 1 (mTORC1) nutrient sensor activation in response to toll-like receptor agonists.
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Induction of protective immunity against Schistosoma mansoni by a non-living vaccine. VI. Antigen recognition by non-responder mouse strains.
TL;DR: The hypothesis that the intradermal vaccine acts through induction of T‐cell‐mediated immune resistance mechanisms is strengthened, as vaccinated P and BALB/c mice showed specific defects in cell‐mediated immunity to schistosome antigens, including decreased production of macrophage‐activating lymphokines and an inability to produce activated macrophages at the site of antigen challenge.
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Reappraisal of the guinea-pig as an experimental host for studies of schistosomiasis mansoni.
TL;DR: The guinea-pig has been reassessed as a potential laboratory host for Schistosoma mansoni and the fact that schistosome eggs are deposited in the lungs of these animals indicates that portal systemic anastomosis is a feature of the model.