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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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Schistosoma mansoni infection-induced transcriptional changes in hepatic macrophage metabolism correlate with an athero-protective phenotype

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.
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Reverse genetics and the study of the immune response to schistosomes.

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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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.

Edward J. Pearce, +1 more
- 01 Dec 1983 - 
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.