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2011 Jornada Científica de la Sociedad Española de Arcillas 14 de ...

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<strong>Jornada</strong> Científica <strong>de</strong> <strong>la</strong> <strong>Sociedad</strong> Españo<strong>la</strong> <strong>de</strong> Arcil<strong>la</strong>s. <strong>14</strong> <strong>de</strong> Noviembre <strong>de</strong> <strong>2011</strong><br />

LIPID-BASED BIO-NANOHYBRIDS FOR THERMAL STABILIZATION OF<br />

VIRAL SPECIES AND APPLICATION AS INFLUENZA VACCINES<br />

B. Wicklein*, M.A. Martin <strong>de</strong>l Burgo**, M. Yuste**, M. Dar<strong>de</strong>r*, P. Aranda*, J.<br />

Ortin***, G. <strong>de</strong>l Real**, E. Ruiz-Hitzky*<br />

*Instituto <strong>de</strong> Ciencia <strong>de</strong> Materiales <strong>de</strong> Madrid, CSIC. Cantob<strong>la</strong>nco, 28049<br />

Madrid<br />

**Instituto Nacional <strong>de</strong> Investigación y Tecnología Agraria y Alimentaria, Ctra.<br />

<strong>de</strong> <strong>la</strong> Coruña Km 7,5, 28040 Madrid<br />

***Centro Nacional <strong>de</strong> Biotecnología, CSIC, Cantob<strong>la</strong>nco, 28049 Madrid<br />

We report the preparation and efficacy testing of influenza A vaccines<br />

composed of bio-nanohybrids based on phospholipid modified c<strong>la</strong>ys [1] as<br />

carrier for either inactivated influenza A virus particles (PR8/H1N1) or the main<br />

surface influenza antigen hemagglutinin (HA) (Fig. 1A and B) [2]. Thermal<br />

stabilization of vaccines during shipment and distribution is a challenging task,<br />

especially in <strong>de</strong>veloping countries. To address this question, we have <strong>de</strong>signed<br />

a novel carrier p<strong>la</strong>tform based on two types of c<strong>la</strong>ys, sepiolite and Mg/Al type<br />

<strong>la</strong>yered double hydroxi<strong>de</strong>, disp<strong>la</strong>ying biomimetic lipid interfaces to ensure native<br />

and maximum stability of immobilized antigens. It is well known that solid<br />

adjuvants as vaccine carriers may inflict conformational alterations on the<br />

antigen by strong interactions and thus, diminish its immunogenic potential [3].<br />

Therefore, lipid bi<strong>la</strong>yer membranes are incorporated to modu<strong>la</strong>te these<br />

interactions. In addition to the use of the whole viral particle, the surface antigen<br />

HA was also immobilized on the lipid interface mimicking its localization on the<br />

viral membrane. As a result, these vaccine modifications preserved the<br />

biological nature of the antigens (Fig. 1C), elicited virus-specific antibodies in<br />

mice and showed higher thermal stability as compared to aluminum salts, the<br />

currently most wi<strong>de</strong>ly used antigenic adjuvant [4].<br />

87

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