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ANNUAL REPORT - Pevion Biotech AG

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Ultrastructure of virosomes<br />

Virosomes are spherical, unilamellar vesicles with a mean diameter of 150<br />

nm. Essentially, virosomes represent reconstituted empty influenza virus<br />

envelopes devoid of the nucleocapsid<br />

including the genetic material of the source<br />

virus. Virosomes are not able to replicate but<br />

are pure fusion-active vesicles. They function<br />

as both carrier platforms and adjuvants. In<br />

contrast to liposomes, virosomes contain<br />

functional viral envelope glycoproteins:<br />

influenza virus hemagglutinin (HA) and<br />

neuraminidase (NA) intercalated in the<br />

phospholipid bilayer membrane. The unique<br />

properties of virosomes partially relate to the<br />

presence of these glycoproteins. They not<br />

only confer structural stability and<br />

homogeneity to virosome formulations, but<br />

they significantly contribute to the<br />

immunological properties of virosomes, which<br />

are clearly distinct from other liposomal and<br />

proteoliposomal carrier systems. These<br />

proteins enable the virosome membranes to<br />

fuse with cells of the immune system and thus<br />

deliver their contents – the specific antigens –<br />

directly to their target cells, eliciting a specific first-class immune response<br />

even with weak-immunogenic antigens. Once they have delivered the<br />

antigens, the virosomes are completely metabolized, whereas the<br />

conventional adjuvant aluminum stays in the body. Thus virosomes are an<br />

efficient and safe carrier and adjuvant system.<br />

PeviPRO TM<br />

PeviPRO TM is <strong>Pevion</strong> <strong>Biotech</strong>’s proprietary virosome carrier platform for the<br />

development of antigen-specific prophylactic vaccines. Vaccines based on<br />

PeviPRO TM generate high quality humoral immune responses and longlasting<br />

protection, even with weak immunogens (for instance peptide<br />

antigens). A main focus in <strong>Pevion</strong> <strong>Biotech</strong>’s own developments is the<br />

PeviPROTM-based malaria vaccine, which completed clinical Phase I in Q2<br />

2005.<br />

PeviTER TM<br />

Hemagglutinin<br />

Neuraminidase<br />

Phosphatidylcholine<br />

Phosphatidylethanolamine<br />

Figure 2: Ultrastructure of<br />

virosomes<br />

PeviTER TM is <strong>Pevion</strong> <strong>Biotech</strong>’s proprietary virosome carrier platform for the<br />

development of T-cell antigen specific therapeutic vaccines against chronic<br />

infectious diseases as well as other diseases including cancer. Vaccines<br />

based on PeviTER TM generate a highly specific cellular immune response.<br />

<strong>Pevion</strong> <strong>Biotech</strong>’s hepatitis C (HCV) vaccine uses the PeviTER TM approach by<br />

encapsulating T-cell epitopes into virosomes and exposing them to the<br />

immune system via the MHC class I/II pathway.<br />

PeviPHAR<br />

PeviPHAR is <strong>Pevion</strong> <strong>Biotech</strong>’s proprietary technology platform for drug<br />

antisense and DNA delivery. Using specific receptors/ligands or<br />

antigens/antibodies interactions, the virosomes will be targeted to specific<br />

cells. Drugs, encapsulated into virosomes, will mainly be delivered to the<br />

targeted cells, which will reduce the amount of the drug used and will also<br />

diminish the toxic effects. A main focus is the site-specific delivery of<br />

cytostatics in cancer therapy.<br />

<strong>Pevion</strong> <strong>Biotech</strong>_Annual Report2005_01_01_04_004 8/13

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