Abstract |
Exosomes have been proposed as candidates for therapeutic immunization. The present study demonstrates that incorporation of the G protein of vesicular stomatitis virus (VSV-G) into exosome-like vesicles (ELVs) enhances their uptake and induces the maturation of dendritic cells. Targeting of VSV-G and ovalbumin as a model antigen to the same ELVs increased the cross-presentation of ovalbumin via an endosomal acidification mechanism. Immunization of mice with VSV-G and ovalbumin containing ELVs led to an increased IgG2a antibody response, expansion of antigen-specific CD8 T cells, strong in vivo CTL responses, and protection from challenge with ovalbumin expressing tumor cells. Thus, incorporation of VSV-G and targeting of antigens to ELVs are attractive strategies to improve exosomal vaccines.
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Authors | Vladimir V Temchura, Matthias Tenbusch, Godwin Nchinda, Ghulam Nabi, Bettina Tippler, Maryna Zelenyuk, Oliver Wildner, Klaus Uberla, Seraphin Kuate |
Journal | Vaccine
(Vaccine)
Vol. 26
Issue 29-30
Pg. 3662-72
(Jul 04 2008)
ISSN: 0264-410X [Print] Netherlands |
PMID | 18538453
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antibodies
- G protein, vesicular stomatitis virus
- Membrane Glycoproteins
- Vaccines
- Viral Envelope Proteins
- Ovalbumin
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Topics |
- Animals
- Antibodies
(blood)
- Antigen Presentation
- CD8-Positive T-Lymphocytes
(immunology)
- Cytotoxicity, Immunologic
- Dendritic Cells
(immunology)
- Endosomes
(metabolism)
- Humans
- Membrane Glycoproteins
(immunology)
- Mice
- Mice, Inbred C57BL
- Neoplasms
(prevention & control)
- Ovalbumin
(immunology)
- Protein Transport
- Secretory Vesicles
(immunology)
- Vaccines
(immunology)
- Viral Envelope Proteins
(immunology)
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