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Doina Ganea

Researcher at Temple University

Publications -  152
Citations -  10552

Doina Ganea is an academic researcher from Temple University. The author has contributed to research in topics: Vasoactive intestinal peptide & Immune system. The author has an hindex of 67, co-authored 152 publications receiving 9947 citations. Previous affiliations of Doina Ganea include Rutgers University & Indiana University.

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Journal ArticleDOI

The Significance of Vasoactive Intestinal Peptide in Immunomodulation

TL;DR: Recognition of the central functions VIP plays in cellular processes is focusing attention on this “very important peptide” as exciting new candidates for therapeutic intervention and drug development.
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The Proinflammatory Effect of Prostaglandin E2 in Experimental Inflammatory Bowel Disease Is Mediated through the IL-23→IL-17 Axis

TL;DR: It is proposed that high levels of PGE2 exacerbate the inflammatory process in inflammatory bowel disease through the preferential expression and release of DC-derived IL-23 and the subsequent support of the autoreactive/inflammatory Th17 phenotype.
Journal Article

Vasoactive Intestinal Peptide (VIP) and Pituitary Adenylate Cyclase-Activation Polypeptide (PACAP) Protect Mice from Lethal Endotoxemia Through the Inhibition of TNF-α and IL-6

TL;DR: The neuropeptides VIP/PACAP protect from the lethal effect of high endotoxemia, presumably by down-regulating TNF-α and IL-6 production, and may offer an alternative in the treatment of human septic shock syndrome.
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Vasoactive Intestinal Peptide and Pituitary Adenylate Cyclase-Activating Polypeptide Enhance IL-10 Production by Murine Macrophages: In Vitro and In Vivo Studies

TL;DR: The stimulation of IL-10 production in activated macrophages represents a novel anti-inflammatory activity of VIP and PACAP, which presumably acts in vivo in conjunction with the inhibition of proinflammatory cytokines such as IL-6 and TNF-alpha to reduce the magnitude of the immune response.
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Prostaglandin E2 induces IL-23 production in bone marrow-derived dendritic cells

TL;DR: The results indicate that PGE2 increases the production of functional IL‐23 from immature BM‐DCs in a time‐ and dose‐dependent manner, and suggest an additional mechanism for its pro‐ inflammatory role, particularly significant for autoimmune diseases, such as rheumatoid arthritis.