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Carlos A. Guzmán

Researcher at University of Genoa

Publications -  281
Citations -  10481

Carlos A. Guzmán is an academic researcher from University of Genoa. The author has contributed to research in topics: Immune system & Antigen. The author has an hindex of 54, co-authored 260 publications receiving 9506 citations. Previous affiliations of Carlos A. Guzmán include Hannover Medical School & Bill & Melinda Gates Foundation.

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In Silico Vaccine Strain Prediction for Human Influenza Viruses

TL;DR: Computational techniques should already be incorporated into the vaccine-selection process in an independent, parallel track, and their performance continuously evaluated.
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Interaction of Salmonella enterica serotype Typhimurium with dendritic cells is defined by targeting to compartments lacking lysosomal membrane glycoproteins.

TL;DR: The capacity of serotype Typhimurium to survive within the established mouse DC line CB1 is shown and it is shown that the PhoPQ two-component regulatory system is not essential for pathogen intracellular survival.
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Pidotimod promotes functional maturation of dendritic cells and displays adjuvant properties at the nasal mucosa level.

TL;DR: Pidotimod is demonstrated to induce DC maturation and up-regulate the expression of HLA-DR and co-stimulatory molecules CD83 and CD86, which are fundamental for communication with adaptative immunity cells, and to promote an effective mucosal and systemic immune response.
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A New RNA-Based Adjuvant Enhances Virus-Specific Vaccine Responses by Locally Triggering TLR- and RLH-Dependent Effects.

TL;DR: Vaccinating mice with an influenza subunit vaccine with RNAdjuvant significantly enhanced this IgG1 and additionally promoted the formation of IgG2b/c, which is indicative of Th1 responses, and upon vaccination with virus-like particles displaying vesicular stomatitis virus G protein, mice were protected against lethal virus infection.
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Dendritic Cell–Mediated Immune Humanization of Mice: Implications for Allogeneic and Xenogeneic Stem Cell Transplantation

TL;DR: Adoptive immunotherapy with engineered DC provides a novel strategy for de novo immune reconstitution after human HCT and a practical and effective tool for studying human lymphatic regeneration in vivo in immune deficient xenograft hosts.