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Immunization with Genetically Modified Trypanosomes Provides Protection against Transmissible Spongiform Encephalopathies.
Triller, Gianna; Garyfallos, Dimitrios A; Papavasiliou, F Nina; Sklaviadis, Theodoros; Stavropoulos, Pete; Xanthopoulos, Konstantinos.
Afiliação
  • Triller G; Laboratory of Lymphocyte Biology, The Rockefeller University, New York, NY 10065, USA.
  • Garyfallos DA; Cambridge Institute of Therapeutic Immunology & Infectious Disease (CITIID), University of Cambridge, Puddicombe Way, Cambridge CB2 0AW, UK.
  • Papavasiliou FN; Division of Immune Diversity, Deutsches Krebsforschungszentrum, 69120 Heidelberg, Germany.
  • Sklaviadis T; Laboratory of Pharmacology, School of Pharmacy, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
  • Stavropoulos P; Laboratory of Lymphocyte Biology, The Rockefeller University, New York, NY 10065, USA.
  • Xanthopoulos K; Laboratory of Pharmacology, School of Pharmacy, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
Int J Mol Sci ; 23(18)2022 Sep 13.
Article em En | MEDLINE | ID: mdl-36142526
ABSTRACT
Transmissible spongiform encephalopathies are incurable neurodegenerative diseases, associated with the conversion of the physiological prion protein to its disease-associated counterpart. Even though immunization against transmissible spongiform encephalopathies has shown great potential, immune tolerance effects impede the use of active immunization protocols for successful prophylaxis. In this study, we evaluate the use of trypanosomes as biological platforms for the presentation of a prion antigenic peptide to the host immune system. Using the engineered trypanosomes in an immunization protocol without the use of adjuvants led to the development of a humoral immune response against the prion protein in wild type mice, without the appearance of adverse reactions. The immune reaction elicited with this protocol displayed in vitro therapeutic potential and was further evaluated in a bioassay where immunized mice were partially protected in a representative murine model of prion diseases. Further studies are underway to better characterize the immune reaction and optimize the immunization protocol.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trypanosoma / Príons / Doenças Priônicas Tipo de estudo: Guideline Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Trypanosoma / Príons / Doenças Priônicas Tipo de estudo: Guideline Limite: Animals Idioma: En Ano de publicação: 2022 Tipo de documento: Article