Immunogenicity of a virosomally-formulated Plasmodium falciparum GLURP-MSP3 chimeric protein-based malaria vaccine candidate in comparison to adjuvanted formulations

Research output: Contribution to journalJournal articleResearchpeer-review

  • Marco Tamborrini
  • Sabine A Stoffel
  • Nicole Westerfeld
  • Mario Amacker
  • Theisen, Michael
  • Rinaldo Zurbriggen
  • Gerd Pluschke
In clinical trials, immunopotentiating reconstituted influenza virosomes (IRIVs) have shown great potential as a versatile antigen delivery platform for synthetic peptides derived from Plasmodium falciparum antigens. This study describes the immunogenicity of a virosomally-formulated recombinant fusion protein comprising domains of the two malaria vaccine candidate antigens MSP3 and GLURP.
Original languageEnglish
JournalMalaria Journal
Volume10
Pages (from-to)359
ISSN1475-2875
DOIs
Publication statusPublished - 2011

    Research areas

  • Adjuvants, Immunologic, Animals, Antibodies, Protozoan, Antigens, Protozoan, Cross Reactions, Immunoglobulin G, Injections, Intramuscular, Malaria Vaccines, Mannitol, Mice, Oleic Acids, Plasmodium falciparum, Protozoan Proteins, Recombinant Fusion Proteins, Vaccines, Synthetic, Vaccines, Virosome

ID: 37835014