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Verfasst von:Nassal, Michael [VerfasserIn]   i
 Skamel, Claudia [VerfasserIn]   i
 Kratz, Peter A. [VerfasserIn]   i
 Wallich, Reinhard [VerfasserIn]   i
 Stehle, Thomas [VerfasserIn]   i
 Simon, Markus M. [VerfasserIn]   i
Titel:A fusion product of the complete Borrelia burgdorferi outer surface protein A (OspA) and the hepatitis B virus capsid protein is highly immunogenic and induces protective immunity similar to that seen with an effective lipidated OspA vaccine formula
Verf.angabe:Michael Nassal, Claudia Skamel, Peter A. Kratz, Reinhard Wallich, Thomas Stehle and Markus M. Simon
Jahr:2005
Umfang:11 S.
Teil:volume:35
 year:2005
 number:2
 pages:655-665
 extent:11
Fussnoten:Gesehen am 04.06.2021
Titel Quelle:Enthalten in: European journal of immunology
Ort Quelle:Weinheim : Wiley-VCH, 1971
Jahr Quelle:2005
Band/Heft Quelle:35(2005), 2, Seite 655-665
ISSN Quelle:1521-4141
Abstract:The immunogenicity of peptides and protein fragments can be considerably enhanced by their presentation on particulate carriers such as capsid-like particles (CLP) from hepatitis B virus (HBV). Here we tested the suitability of the HBV capsid protein as a carrier for a relevant full-length pathogen-derived protein antigen. The entire 255-amino acid ectodomain of the outer surface protein A (OspA) from Borrelia burgdorferi, the causative agent of Lyme disease, was inserted into the major B cell epitope of the HBV capsid, yielding a multimerization-competent fusion protein, termed coreOspA. CoreOspA, consisting only in part of regular CLP, induced antibodies to OspA, including the Ig isotype profile and specificity for the protective epitope LA-2, with an efficiency similar to that of recombinant lipidated OspA, the first generation vaccine against Lyme disease. Moreover, coreOspA actively and passively protected mice against subsequent challenge with B. burgdorferi. The data demonstrate the capacity of the HBV capsid protein to act as a potent immunomodulator even for full-length and structurally complex polypeptide chains and thus opens new avenues for novel vaccine designs.
DOI:doi:10.1002/eji.200425449
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/https://doi.org/10.1002/eji.200425449
 Volltext: https://onlinelibrary.wiley.com/doi/full/10.1002/eji.200425449
 DOI: https://doi.org/10.1002/eji.200425449
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Animals
 Antigens, Surface
 Bacterial Outer Membrane Proteins
 Bacterial Vaccines
 Borrelia burgdorferi
 Capsid Proteins
 Female
 Hepatitis B Antigens
 Hepatitis B virus
 Lipid Metabolism
 Lipoproteins
 Lyme Disease
 Lyme Disease Vaccines
 Mice
 Mice, Inbred BALB C
 Mice, SCID
 Protein Structure, Tertiary
 Recombinant Fusion Proteins
K10plus-PPN:1759809128
Verknüpfungen:→ Zeitschrift

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